Chromatography Standards

CERTIPUR is a registered trademark of Merck KGaA, Darmstadt, Germany

Sulfathiazole is a broad-spectrum antibacterial drug, belonging to the class of sulfonamides, used in veterinary and human medication for the treatment of infections. It is also involved in promoting growth of livestock and fish.

storage conditions	Store at +15°C to +25°C.
Quality Level	100
application(s)	ion chromatography: suitable
density	0.998 g/cm³ at 20 °C
Featured Industry	Environmental Food and Beverages
format	single component solution
storage temp.	15-25°C

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Sulfathiazole

Empirical Formula (Hill Notation):	C₉H₉N₃O₂S₂
CAS Number:	72-14-0
Molecular Weight:	255.32
Beilstein/REAXYS Number:	226178
EC Number:	200-771-5
MDL number:	MFCD00005319
PubChem Substance ID:	329824636
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Sulfathiazole is used as an analytical reference standard for the quantification of the analyte in meat, and honey samples using different chromatography techniques.

100, 250 g in poly bottle

Sulfonamide antibiotic that blocks the synthesis of dihydrofolic acid by inhibiting the enzyme dihydropteroate synthase.
Mode of Action: Inhibits folic acid synthesis in prokaryotes.
Anti-microbial Spectrum: Gram positive, Gram negative, Chlamydia
Mode of Resistance: Alteration of dihydropteroate synthase or alternative pathway for folic acid synthesis.

Quality Level	100
grade	analytical standard
Agency/Method	EPA 1694
assay	99.0-101.0% (EP)
form	powder
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	200-202 °C (lit.)
Featured Industry	Clinical Environmental Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
SMILES string	Nc1ccc(cc1)S(=O)(=O)Nc2nccs2
InChI	1S/C9H9N3O2S2/c10-7-1-3-8(4-2-7)16(13,14)12-9-11-5-6-15-9/h1-6H,10H2,(H,11,12)
InChI key	JNMRHUJNCSQMMB-UHFFFAOYSA-N

Chemical structure: sulfonamide

pictograms	GHS07
signalword	Warning
hcodes	H315 - H319 - H335 - H412
pcodes	P261 - P264 - P271 - P273 - P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 2

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Sulfathiazole-(phenyl-13C6)

Empirical Formula (Hill Notation):	¹³C₆C₃H₉N₃O₂S₂
CAS Number:	1196157-72-8
Molecular Weight:	261.27
MDL number:	MFCD16652579
PubChem Substance ID:	329754265
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	100
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Clinical Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
mass shift	M+6
SMILES string	N[13c]1[13cH][13cH][13c]([13cH][13cH]1)S(=O)(=O)Nc2nccs2
InChI	1S/C9H9N3O2S2/c10-7-1-3-8(4-2-7)16(13,14)12-9-11-5-6-15-9/h1-6H,10H2,(H,11,12)/i1+1,2+1,3+1,4+1,7+1,8+1
InChI key	JNMRHUJNCSQMMB-UQUYMPKGSA-N

Chemical structure: sulfonamide

pictograms	GHS07
signalword	Warning
hcodes	H315 - H319 - H335 - H412
pcodes	P261 - P264 - P271 - P273 - P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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Sulfisomidin

Empirical Formula (Hill Notation):	C₁₂H₁₄N₄O₂S
CAS Number:	515-64-0
Molecular Weight:	278.33
Beilstein/REAXYS Number:	261305
EC Number:	208-204-3
MDL number:	MFCD00010567
PubChem Substance ID:	329757260
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	200
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	242-243 °C (lit.)
Featured Industry	Clinical Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
SMILES string	Cc1cc(NS(=O)(=O)c2ccc(N)cc2)nc(C)n1
InChI	1S/C12H14N4O2S/c1-8-7-12(15-9(2)14-8)16-19(17,18)11-5-3-10(13)4-6-11/h3-7H,13H2,1-2H3,(H,14,15,16)
InChI key	YZMCKZRAOLZXAZ-UHFFFAOYSA-N

Sulfolane is widely used in combination with diisopropanolamine in the sulfinol process of removal of toxic levels of hydrogen sulfide and carbonyl sulfide from raw natural gas condensate. It is also used as an industrial solvent for photographic chemicals, polymer, and petrochemical industries.
Sulfolane is an aprotic polar solvent, used in the separation of aromatic hydrocarbons from aliphatic hydrocarbons.

pictograms	GHS07
signalword	Warning
hcodes	H315 - H319 - H335
pcodes	P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 2

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Sulfolane

Empirical Formula (Hill Notation):	C₄H₈O₂S
CAS Number:	126-33-0
Molecular Weight:	120.17
Beilstein/REAXYS Number:	107765
EC Number:	204-783-1
MDL number:	MFCD00005484
PubChem Substance ID:	329769680
NACRES:	NA.24

Sulfolane may be used as an analytical reference standard for the quantification of the analyte in groundwater samples using gas chromatography-mass spectrometry technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Quality Level	100
grade	analytical standard
vapor density	4.2 (vs air)
vapor pressure	0.01 mmHg ( 20 °C)
assay	99.8% (GC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.484 (lit.), n20/D 1.485
bp	104 °C/0.2 mmHg (lit.), 285 °C (lit.)
mp	20-26 °C (lit.)
density	1.261 g/mL at 25 °C (lit.)
Featured Industry	Environmental
format	neat
SMILES string	O=S1(=O)CCCC1
InChI	1S/C4H8O2S/c5-7(6)3-1-2-4-7/h1-4H2
InChI key	HXJUTPCZVOIRIF-UHFFFAOYSA-N

Treatment of human colorectal cancer cell lines induces MRP1 and MRP3 but not other members of the MRP family. Reported to significantly increase the cytotoxicity of the anthracyclines (doxorubicin, daunorubicin and epirubicin), as well as teniposide, VP-16 and vincristine. Sulindac was tested for its effect on heat-induced denaturation of albumin in vitro28 and its ability to bind to human plasma protein.29

pictograms	GHS07,GHS08
signalword	Danger
hcodes	H302 - H360FD
pcodes	P202 - P264 - P270 - P280 - P301 + P312 - P308 + P313
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point F	350.6 °F - closed cup
Flash Point C	177 °C - closed cup

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Sulindac

Empirical Formula (Hill Notation):	C₂₀H₁₇FO₃S
CAS Number:	38194-50-2
Molecular Weight:	356.41
EC Number:	253-819-2
MDL number:	MFCD00599589
PubChem Substance ID:	57654635
NACRES:	NA.77

5, 25 g in poly bottle

Sulindac is non-steroidal anti-inflammatory drug and an analgesic that has antiproliferative and apoptotic effects. It inhibits the expression and activity of cyclooxygenase-2 in human colon cancer cells25,26 and reduces tumor burden in adenomatous polyposis patients.27
Nonsteroidal anti-inflammatory; preferential inhibitor of COX-1.

Features and Benefits

This compound was developed by Merck & Co., Inc., Kenilworth, NJ, U.S.. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.
This compound is also offered as part of Sigmas Library of Pharmacologically Active Compounds (LOPAC®1280), a biologically annotated collection of high-quality, ready-to-screen compounds. Click here to learn more.
This compound is a featured product for ADME Tox research. Click here to discover more featured ADME Tox products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

LOPAC is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	200
biological source	synthetic (organic)
assay	98.0%
form	powder
application(s)	HPLC: suitable, gas chromatography (GC): suitable
solubility	methanol: 50 mg/mL
Featured Industry	Forensics and Toxicology Veterinary
originator	Merck & Co., Inc., Kenilworth, NJ, U.S.
SMILES string	CC1=C(CC(O)=O)c2cc(F)ccc2\C1=C/c3ccc(cc3)S(C)=O
InChI	1S/C20H17FO3S/c1-12-17(9-13-3-6-15(7-4-13)25(2)24)16-8-5-14(21)10-19(16)18(12)11-20(22)23/h3-10H,11H2,1-2H3,(H,22,23)/b17-9-
InChI key	MLKXDPUZXIRXEP-MFOYZWKCSA-N
Gene Information	human ... ALB(213), PTGS1(5742), PTGS2(5743)

Sulisobenzone is a broad spectrum organic UV filter in sunscreen formulations, known to absorb deleterious UV light.

pictograms	GHS06,GHS08
signalword	Danger
hcodes	H301 - H317 - H334 - H361
pcodes	P201 - P280 - P301 + P310 + P330 - P302 + P352
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
RIDADR	UN 2811 6.1 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Sulisobenzone

Empirical Formula (Hill Notation):	C₁₄H₁₂O₆S
CAS Number:	4065-45-6
Molecular Weight:	308.31
Beilstein/REAXYS Number:	2889165
EC Number:	223-772-2
MDL number:	MFCD00024962
PubChem Substance ID:	329757575
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Sulisobenzone may be used as an analytical reagent for the determination of the analyte in sunscreen formulations by high-performance liquid chromatography with UV spectrophotometric detection.

100 mg in glass bottle
Bottomless glass bottle. Contents are inside inserted fused cone.

grade	analytical standard
Quality Level	100
assay	97.5% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Cleaning Products Cosmetics Environmental Food and Beverages Personal Care
format	neat
SMILES string	COc1cc(O)c(cc1S(O)(=O)=O)C(=O)c2ccccc2
InChI	1S/C14H12O6S/c1-20-12-8-11(15)10(7-13(12)21(17,18)19)14(16)9-5-3-2-4-6-9/h2-8,15H,1H3,(H,17,18,19)
InChI key	CXVGEDCSTKKODG-UHFFFAOYSA-N

Sunset Yellow FCF azo-dye is generally used as a colorant in drug industries and in common foods.

pictograms	GHS07
signalword	Warning
hcodes	H315 - H319 - H412
pcodes	P273 - P302 + P352 - P305 + P351 + P338
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point F	No data available
Flash Point C	No data available

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Sunset Yellow FCF

Empirical Formula (Hill Notation):	C₁₆H₁₀N₂Na₂O₇S₂
CAS Number:	2783-94-0
Molecular Weight:	452.37
Colour Index Number:	15985
EC Number:	220-491-7
MDL number:	MFCD00036437
PubChem Substance ID:	329761152
E Number:	E110
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Bottomless glass bottle. Contents are inside inserted fused cone.

grade	analytical standard
Quality Level	100
assay	95% (HPLC)
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	>300 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Food and Beverages Personal Care
format	neat
SMILES string	[Na+].[Na+].Oc1ccc2cc(ccc2c1\N=N\c3ccc(cc3)S([O-])(=O)=O)S([O-])(=O)=O
InChI	1S/C16H12N2O7S2.2Na/c19-15-8-1-10-9-13(27(23,24)25)6-7-14(10)16(15)18-17-11-2-4-12(5-3-11)26(20,21)22;;/h1-9,19H,(H,20,21,22)(H,23,24,25);;/q;2*+1/p-2/b18-17+;;
InChI key	OIQPTROHQCGFEF-QIKYXUGXSA-L

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 2
Flash Point F	Not applicable
Flash Point C	Not applicable

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Tamoxifen

Empirical Formula (Hill Notation):	C₂₆H₂₉NO
Linear Formula:	C₆H₅C(C₂H₅)=C(C₆H₅)C₆H₄OCH₂CH₂N(CH₃)₂
CAS Number:	10540-29-1
Molecular Weight:	371.51
EC Number:	234-118-0
MDL number:	MFCD00010454
PubChem Substance ID:	329769367

Protein kinase C inhibitor. Induces apoptosis in human malignant glioma cell lines. Tamoxifen and its metabolite 4-hydroxytamoxifen are selective estrogen response modifiers (SERMs) that act as estrogen antagonists in mammary gland. Blocks estradiol-stimulated VEGF production in breast tumor cells.

Quality Level	100
grade	analytical standard
assay	98.0% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
impurities	0.5% water
mp	97-98 °C (lit.)
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
storage temp.	2-8°C
SMILES string	CC\C(c1ccccc1)=C(/c2ccccc2)c3ccc(OCCN(C)C)cc3
InChI	1S/C26H29NO/c1-4-25(21-11-7-5-8-12-21)26(22-13-9-6-10-14-22)23-15-17-24(18-16-23)28-20-19-27(2)3/h5-18H,4,19-20H2,1-3H3/b26-25-
InChI key	NKANXQFJJICGDU-QPLCGJKRSA-N
Gene Information	human ... ESR1(2099)

This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the Issuing Pharmacopoeia.

pictograms	GHS08,GHS09
signalword	Danger
hcodes	H350 - H360 - H410
pcodes	P201 - P273 - P308 + P313
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Tamoxifen citrate

Empirical Formula (Hill Notation):	C₂₆H₂₉NO · C₆H₈O₇
CAS Number:	54965-24-1
Molecular Weight:	563.64
MDL number:	MFCD00058321
PubChem Substance ID:	329826577
NACRES:	NA.24

Unit quantity: 60 mg. Subject to change. The product is delivered as supplied by the issuing Pharmacopoeia.

Sales restrictions may apply.

grade	pharmaceutical primary standard
form	neat
Торговая марка	EDQM
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Pharmaceutical (small molecule)
format	neat
storage temp.	2-8°C
SMILES string	OC(=O)CC(O)(CC(O)=O)C(O)=O.CC\C(c1ccccc1)=C(/c2ccccc2)c3ccc(OCCN(C)C)cc3
InChI	1S/C26H29NO.C6H8O7/c1-4-25(21-11-7-5-8-12-21)26(22-13-9-6-10-14-22)23-15-17-24(18-16-23)28-20-19-27(2)3;7-3(8)1-6(13,5(11)12)2-4(9)10/h5-18H,4,19-20H2,1-3H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)/b26-25-;
InChI key	FQZYTYWMLGAPFJ-OQKDUQJOSA-N
Gene Information	human ... ESR1(2099)

Tanshinone I is a bioconstituent, belonging to the class of tanshinone compounds isolated from Salvia miltiorrhiza Bunge. It is commonly used to dilate coronary arteries, increase coronary flow, modulate mutagenic activity and protect the myocardium against ischaemia.

pictograms	GHS07,GHS08,GHS09
signalword	Danger
hcodes	H302 - H350 - H360D - H410
pcodes	P201 - P273 - P301 + P312 + P330 - P308 + P313
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Tanshinone I

Empirical Formula (Hill Notation):	C₁₈H₁₂O₃
CAS Number:	568-73-0
Molecular Weight:	276.29
MDL number:	MFCD00210563
PubChem Substance ID:	329769042
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Tanshinone I may be used as an analytical reference standard for the quantification of the analyte in pharmaceutical formulations and roots of Salvia miltiorrhiza using different chromatography techniques.

Phenanthrenequinone constituent of Chinese medicinal herb Danshen (Salvia miltiorrhiza). Modulates or prevents breast cancer metastasis by regulating adhesion molecules. Anti-inflammatory.

Bottomless glass bottle. Contents are inside inserted fused cone.

Quality Level	100
grade	analytical standard
assay	≥98.0% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Food and Beverages
format	neat
storage temp.	2-8°C
SMILES string	Cc1coc2-c3ccc4c(C)cccc4c3C(=O)C(=O)c12
InChI	1S/C18H12O3/c1-9-4-3-5-12-11(9)6-7-13-15(12)17(20)16(19)14-10(2)8-21-18(13)14/h3-8H,1-2H3
InChI key	AIGAZQPHXLWMOJ-UHFFFAOYSA-N

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Tanshinone IIA

Empirical Formula (Hill Notation):	C₁₉H₁₈O₃
CAS Number:	568-72-9
Molecular Weight:	294.34
MDL number:	MFCD00238692
PubChem Substance ID:	329757732
NACRES:	NA.24

Phenanthrenequinone constituent of Chinese medicinal herb Danshen (Salvia miltiorrhiza). Anti-inflammatory. Antioxidant. Cytotoxic against a variety of cell lines, inlcuding human glioma cells.

Bottomless glass bottle. Contents are inside inserted fused cone.

Quality Level	100
grade	analytical standard
assay	≥98.0% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	204-208 °C
Featured Industry	Food and Beverages
format	neat
storage temp.	2-8°C
SMILES string	Cc1coc2-c3ccc4c(CCCC4(C)C)c3C(=O)C(=O)c12
InChI	1S/C19H18O3/c1-10-9-22-18-12-6-7-13-11(5-4-8-19(13,2)3)15(12)17(21)16(20)14(10)18/h6-7,9H,4-5,8H2,1-3H3
InChI key	HYXITZLLTYIPOF-UHFFFAOYSA-N

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to SI unit kg and measured against primary material from an NMI, e.g. NIST.
Certified content incl. uncertainty and expiry date are given on the label.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Tartrate Standard for IC

Analysis Note

1000 mg/L tartrate in water, prepared with tartaric acid and water; filtered through a 0.2 μm membrane filter and stabilized with sodium azide

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	300
grade	certified reference material, TraceCERT^®
product line	TraceCERT^®
concentration	1000 mg/L tartrate in water
application(s)	ion chromatography: suitable
Featured Industry	Cleaning Products Cosmetics Environmental Food and Beverages Personal Care
format	single component solution

Tartrazine is a synthetic azo dye, commonly found in drugs, food products and cosmetics. It can be synthesized by the reaction of sulfanilic acid with 3-carboxy-l-(4-sulfophenyl)-5-pyrazolone.

RIDADR	NONH for all modes of transport
WGK Germany	nwg
Flash Point F	Not applicable
Flash Point C	Not applicable

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Tartrazine

Empirical Formula (Hill Notation):	C₁₆H₉N₄Na₃O₉S₂
CAS Number:	1934-21-0
Molecular Weight:	534.36
Colour Index Number:	19140
Beilstein/REAXYS Number:	69850
EC Number:	217-699-5
MDL number:	MFCD00148908
PubChem Substance ID:	329747588
E Number:	E102
NACRES:	NA.24

Tartrazine may be used as reference standard for the determination of tartrazine in commercial soft drinks using thin layer chromatography and ion-pair high performance liquid chromatography.

Bottomless glass bottle. Contents are inside inserted fused cone.

grade	analytical standard
Quality Level	100
assay	99.0% (HPLC)
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Cleaning Products Cosmetics Food and Beverages Personal Care
format	neat
SMILES string	[Na+].[Na+].[Na+].[O-]C(=O)C1=NN(c2ccc(cc2)S([O-])(=O)=O)C(=O)C1N=Nc3ccc(cc3)S([O-])(=O)=O
InChI	1S/C16H12N4O9S2.3Na/c21-15-13(18-17-9-1-5-11(6-2-9)30(24,25)26)14(16(22)23)19-20(15)10-3-7-12(8-4-10)31(27,28)29;;;/h1-8,13H,(H,22,23)(H,24,25,26)(H,27,28,29);;;/q;3*+1/p-3
InChI key	UJMBCXLDXJUMFB-UHFFFAOYSA-K

Taxifolin is a plant flavonoid, which may find applications in the treatment of coronary heart disease, angina pectoris, cerebral thrombosis, cerebral infarction and sequelae.

Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Faceshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1

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Taxifolin

Empirical Formula (Hill Notation):	C₁₅H₁₂O₇
CAS Number:	480-18-2
Molecular Weight:	304.25
Beilstein/REAXYS Number:	5299277
EC Number:	207-543-4
MDL number:	MFCD00006845
PubChem Substance ID:	329768169
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Taxifolin can be used as a reference standard for the determination of taxifolin in plasma of rabbit using high performance liquid chromatography technique(HPLC).

Bottomless glass bottle. Contents are inside inserted fused cone.

Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. 78666.pdf Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.

grade	analytical standard
Quality Level	100
assay	≥85% (HPLC)
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Food and Beverages
format	neat
SMILES string	O[C@@H]1[C@H](Oc2cc(O)cc(O)c2C1=O)c3ccc(O)c(O)c3
InChI	1S/C15H12O7/c16-7-4-10(19)12-11(5-7)22-15(14(21)13(12)20)6-1-2-8(17)9(18)3-6/h1-5,14-19,21H/t14-,15+/m0/s1
InChI key	CXQWRCVTCMQVQX-LSDHHAIUSA-N

Temozolomide (TMZ) is an alkylating agent of the imidazotetrazine derivatives that shows broad-spectrum antitumor activity against murine tumors.

Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Temozolomide

Empirical Formula (Hill Notation):	C₆H₆N₆O₂
CAS Number:	85622-93-1
Molecular Weight:	194.15
MDL number:	MFCD00866492
PubChem Substance ID:	329767423
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
TMZ may be used as a reference standard for the analysis of temozolomide in serum and brain tumor samples by micellar electrokinetic capillary chromatography (MEKC), in aqueous solutions by liquid chromatography-electrospray-tandem mass spectrometry (LC-ESI-MS/MS), in active pharmaceutical ingredients (APIs) by high performance liquid chromatography (HPLC) with MS/MS and in pharmaceutical dosage form by HPLC equipped with photodiode array (PDA) detector.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	100
grade	analytical standard
product line	VETRANAL^®
assay	99.0% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
ign. residue	0.2%
loss	0.5% loss on drying
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
storage temp.	2-8°C
SMILES string	CN1N=Nc2c(ncn2C1=O)C(N)=O
InChI	1S/C6H6N6O2/c1-11-6(14)12-2-8-3(4(7)13)5(12)9-10-11/h2H,1H3,(H2,7,13)
InChI key	BPEGJWRSRHCHSN-UHFFFAOYSA-N

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms	GHS07,GHS08
signalword	Danger
hcodes	H302 - H315 - H319 - H335 - H340 - H350 - H360FD
pcodes	P201 - P202 - P301 + P312 - P302 + P352 - P305 + P351 + P338 - P308 + P313
Target Organs	Respiratory system
Personal Protective Equipment	Eyeshields, Gloves, type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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Terbutaline acetate salt hemihydrate

Empirical Formula (Hill Notation):	C₁₂H₁₉NO₃ · C₂H₄O₂ · 0.5H₂O
Molecular Weight:	294.34
NACRES:	NA.24

Caution

Air Sensitive: Handle under Argon
Light Sensitive: Sensitive

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

grade	analytical standard
Quality Level	100
product line	VETRANAL^®
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
format	neat
SMILES string	O.CC(O)=O.CC(O)=O.CC(C)(C)NCC(O)c1cc(O)cc(O)c1.CC(C)(C)NCC(O)c2cc(O)cc(O)c2

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

192,99 € / 18 154 ₽

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Terbutaline-(tert-butyl-d9) acetate salt hemihydrate

Empirical Formula (Hill Notation):	C₁₂D₉H₁₀NO₃ · C₂H₄O₂ · 0.5H₂O
Molecular Weight:	303.40
NACRES:	NA.24

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

grade	analytical standard
Quality Level	100
product line	VETRANAL^®
form	neat
storage condition	under inert gas
application(s)	HPLC: suitable, gas chromatography (GC): suitable
format	neat
storage temp.	2-8°C
SMILES string	O.CC(O)=O.CC(O)=O.[2H]C([2H])([2H])C(C)(NCC(O)c1cc(O)cc(O)c1)C([2H])([2H])[2H].[2H]C([2H])([2H])C(NCC(O)c2cc(O)cc(O)c2)(C([2H])([2H])[2H])C([2H])([2H])[2H]

Terbuthylazin-desethyl is a triazine herbicide used for the control and elimination of weeds.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

192,99 € / 18 154 ₽

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Terbuthylazin-desethyl

Empirical Formula (Hill Notation):	C₇H₁₂ClN₅
CAS Number:	30125-63-4
Molecular Weight:	201.66
Beilstein/REAXYS Number:	514392
MDL number:	MFCD00144061
PubChem Substance ID:	329753689
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Terbuthylazin-desethyl may be used as a reference standard for the determination of terbuthylazin-desethyl in water samples using dispersed single-walled carbon nanohorns as sorbent and gas chromatography-mass spectrometry as instrumental technique.

PESTANAL is a registered trademark of Sigma-Aldrich International GmbH

grade	analytical standard
Quality Level	100
product line	PESTANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Agriculture Clinical Environmental
format	neat
SMILES string	CC(C)(C)Nc1nc(N)nc(Cl)n1
InChI	1S/C7H12ClN5/c1-7(2,3)13-6-11-4(8)10-5(9)12-6/h1-3H3,(H3,9,10,11,12,13)
InChI key	LMKQNTMFZLAJDV-UHFFFAOYSA-N

Общее описание
Стандарт для картриджей Supelco MIP SPE. Для получения дополнительной информации запросите литературу Supelco T407075, T706023
Тербутилазин-2-гидрокси является метаболитом триазинового гербицида. Он используется для борьбы с однолетними и многолетними сорняками, злаками и широколиственными сорняками в сельскохозяйственных культурах до и после всходов.
Приложение
Для получения дополнительной информации о подходящей методике проведения анализа обратитесь к сертификату на изделие. Обратитесь в техническую службу для получения дополнительной поддержки. Тербутилазин-2-гидрокси может использоваться в качестве аналитического эталона для количественного определения анализируемого вещества в пробах окружающей среды с использованием различных методов хроматографии.
Юридическая информация
PESTANAL является зарегистрированной торговой маркой Sigma-Aldrich International GmbH

Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Faceshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Тербутилазин-2-гидрокси

Empirical Formula (Hill Notation):	C₉H₁₇N₅O
CAS Number:	66753-07-9
Molecular Weight:	211.26
MDL number:	MFCD01632313
PubChem Substance ID:	329757058
NACRES:	NA.24

Информация по технике безопасности

Уровень качества	100
Класс	аналитический стандарт
Линейка продуктов	PESTANAL^®
Форма	аккуратный
Срок годности	ограниченный срок годности, дата истечения срока годности указана на этикетке
Область применения	HPLC: suitable, gas chromatography (GC): suitable, solid phase extraction (SPE): suitable
Избранная отрасль	Сельское хозяйство Экологический
Формат	аккуратный
Строка УЛЫБОК	CCNc1nc(O)nc(NC(C)(C)C)n1
InChI	1S/C9H17N5O/c1-5-10-6-11-7(13-8(15)12-6)14-9(2,3)4/h5H2,1-4H3,(H3,10,11,12,13,14,15)
InChI key	OYTCZOJKXCTBHG-UHFFFAOYSA-N

Пиктограммы	GHS07
Сигнальное слово	Warning
hcodes	H315 - H319 - H335
pcodes	P302 + P352 - P305 + P351 + P338
Target Organs	Дыхательная система
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Непригодный
Flash Point C	Непригодный

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Terconazole

Empirical Formula (Hill Notation):	C₂₆H₃₁Cl₂N₅O₃
CAS Number:	67915-31-5
Molecular Weight:	532.46
EC Number:	267-751-6

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

grade	analytical standard
Quality Level	100
product line	VETRANAL^®
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Veterinary
format	neat
InChI	1S/C26H31Cl2N5O3/c1-19(2)31-9-11-32(12-10-31)21-4-6-22(7-5-21)34-14-23-15-35-26(36-23,16-33-18-29-17-30-33)24-8-3-20(27)13-25(24)28/h3-8,13,17-19,23H,9-12,14-16H2,1-2H3/t23-,26-/m0/s1
InChI key	BLSQLHNBWJLIBQ-OZXSUGGESA-N

tert-Amyl methyl ether (TAME) is a fuel oxygenate which is utilized as an additive in gasoline to enhance the octane rating and to improve combustion.

pictograms	GHS07
signalword	Warning
hcodes	H315 - H319 - H335 - H413
pcodes	P261 - P305 + P351 + P338
Target Organs	Respiratory system
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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tert-Amyl methyl ether 442794

Empirical Formula (Hill Notation):	C₆H₁₄O
Linear Formula:	C₂H₅C(CH₃)₂OCH₃
CAS Number:	994-05-8
Molecular Weight:	102.17
Beilstein/REAXYS Number:	1731452
EC Number:	213-611-4
MDL number:	MFCD00010186
PubChem Substance ID:	24867673

General description

TAME has been used as a reference standard for the determination of the analyte in Catalonian groundwater and soil samples by purge-and-trap gas chromatography/mass spectrometry (P&T-GC/MS) and in aqueous solutions by solid-phase microextraction (SPME) combined with GC-MS. It may be used as a reference standard for the identification of the analyte in gasoline-contaminated groundwater by GC combined with various detectors/quantification methods such as photoionization detector (PID), flame ionization detector (FID), or MS.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Quality Level	200
grade	analytical standard
form	neat
CofA	current certificate can be downloaded
packaging	ampule of 1000 mg
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.389 (lit.), n20/D 1.3896
bp	85-86 °C (lit.)
density	0.76-0.78 g/mL at 25 °C (lit.)
Featured Industry	Environmental
format	neat
storage temp.	room temp
SMILES string	CCC(C)(C)OC
InChI	1S/C6H14O/c1-5-6(2,3)7-4/h5H2,1-4H3
InChI key	HVZJRWJGKQPSFL-UHFFFAOYSA-N

tert-butanol can find applications as an ideal reaction medium or solvent for the lipase-catalyzed biodiesel production.

pictograms	GHS02,GHS07
signalword	Danger
hcodes	H225 - H302 - H336
pcodes	P210 - P301 + P312 + P330
Target Organs	Central nervous system
Personal Protective Equipment	Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
RIDADR	UN 3271 3 / PGII
WGK Germany	WGK 3
Flash Point F	19.4 °F - closed cup
Flash Point C	-7 °C - closed cup

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tert-Butanol

Empirical Formula (Hill Notation):	C₄H₁₀O
Linear Formula:	(CH₃)₃COH
CAS Number:	75-65-0
Molecular Weight:	74.12
Beilstein/REAXYS Number:	906698
EC Number:	200-889-7
MDL number:	MFCD00004464
PubChem Substance ID:	329757613
NACRES:	NA.24

tert-butanol can also find applications in the alkylation of p-cresol to obtain 2-tert-butyl-p-cresol and 2,6-di-tert-butyl-p-cresol, also known as butylated hydroxy toluene, used in the manufacturing of polymerization inhibitors and phenolic resins as antioxidants.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Quality Level	100
grade	analytical standard
vapor density	2.5 (vs air)
vapor pressure	31 mmHg ( 20 °C), 44 mmHg ( 26 °C)
assay	99.8% (GC)
form	neat
autoignition temp.	896 °F
shelf life	limited shelf life, expiry date on the label
expl. lim.	8 %
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.387 (lit.), n20/D 1.387
bp	83 °C (lit.)
mp	23-26 °C (lit.)
density	0.775 g/mL at 25 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Environmental Flavors and Fragrances Food and Beverages Personal Care
format	neat
SMILES string	CC(C)(C)O
InChI	1S/C4H10O/c1-4(2,3)5/h5H,1-3H3
InChI key	DKGAVHZHDRPRBM-UHFFFAOYSA-N

tert-Butyl ethyl ether is a fuel additive used in the formulation of automotive gasoline for reducing the emission of carbon monoxide and unburned hydrocarbons, and also to improve octane ratings.

pictograms	GHS02,GHS07
signalword	Danger
hcodes	H225 - H319 - H332 - H335 - H336
pcodes	P210 - P233 - P240 - P241 - P304 + P340 + P312 - P305 + P351 + P338
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN1120 - class 3 - PG 2 - Butanols
WGK Germany	WGK 1
Flash Point F	59.0 °F - closed cup
Flash Point C	15 °C - closed cup

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tert-Butyl ethyl ether 442795

Empirical Formula (Hill Notation):	C₆H₁₄O
Linear Formula:	C₂H₅OC(CH₃)₃
CAS Number:	637-92-3
Molecular Weight:	102.17
Beilstein/REAXYS Number:	1731469
EC Number:	211-309-7
MDL number:	MFCD00009225
PubChem Substance ID:	24867674

General description

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Quality Level	100
grade	analytical standard
vapor pressure	155 mmHg ( 25 °C)
form	neat
CofA	current certificate can be downloaded
packaging	ampule of 1000 mg
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.375 (lit.)
bp	72-73 °C (lit.)
mp	97 °C (lit.)
density	0.742 g/mL at 25 °C (lit.)
Featured Industry	Environmental
format	neat
storage temp.	room temp
SMILES string	CCOC(C)(C)C
InChI	1S/C6H14O/c1-5-7-6(2,3)4/h5H2,1-4H3
InChI key	NUMQCACRALPSHD-UHFFFAOYSA-N

tert-Butyl methyl ether or methyl tert-butyl ether (MTBE) is an oxygenated compound.. It is commonly used as a gasoline additive in fuel. Though it is known to control air pollution, it is a potential groundwater pollutant.

pictograms	GHS02,GHS07
signalword	Danger
hcodes	H225 - H336
pcodes	P210
Target Organs	Central nervous system
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN 3271 3 / PGII
WGK Germany	WGK 1
Flash Point F	-2.2 °F - closed cup
Flash Point C	-19 °C - closed cup

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tert-Butyl methyl ether

Empirical Formula (Hill Notation):	C₅H₁₂O
Linear Formula:	(CH₃)₃COCH₃
CAS Number:	1634-04-4
Molecular Weight:	88.15
Beilstein/REAXYS Number:	1730942
EC Number:	216-653-1
MDL number:	MFCD00008812
PubChem Substance ID:	329748620
NACRES:	NA.24

MTBE may be used as a reference standard for the determination of MTBE in water by headspace-solid-phase microextraction (headspace-SPME) method.

Quality Level	100
grade	analytical standard
vapor density	3.1 (vs air)
assay	99.9% (GC)
autoignition temp.	705 °F
shelf life	limited shelf life, expiry date on the label
expl. lim.	15.1 %
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.369 (lit.), n20/D 1.369
bp	55-56 °C (lit.)
density	0.74 g/mL at 25 °C (lit.)
Featured Industry	Environmental
format	neat
SMILES string	COC(C)(C)C
InChI	1S/C5H12O/c1-5(2,3)6-4/h1-4H3
InChI key	BZLVMXJERCGZMT-UHFFFAOYSA-N

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms	GHS02,GHS07
signalword	Danger
hcodes	H225 - H315
pcodes	P210 - P302 + P352
Personal Protective Equipment	Eyeshields, Faceshields, Gloves
RIDADR	UN 2398 3 / PGII
WGK Germany	WGK 1
Flash Point F	-18.4 °F - closed cup
Flash Point C	-28 °C - closed cup

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Testosterone solution

CAS Number:	58-22-0
Beilstein/REAXYS Number:	1915399
MDL number:	MFCD00003654
PubChem Substance ID:	329826822
NACRES:	NA.24

1 mL in ampule

grade	drug standard
Quality Level	200
drug control	Home Office Schedule 4.2
concentration	1.0 mg/mL in 1,2-dimethoxyethane
application(s)	HPLC: suitable, gas chromatography (GC): suitable
format	single component solution
storage temp.	2-8°C
SMILES string	[H][C@@]12CCC3=CC(=O)CC[C@]3(C)[C@@]1([H])CC[C@]4(C)[C@@H](O)CC[C@@]24[H]
InChI	1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-17,21H,3-10H2,1-2H3/t14-,15-,16-,17-,18-,19-/m0/s1
InChI key	MUMGGOZAMZWBJJ-DYKIIFRCSA-N
Gene Information	human ... AR(367), EBP(10682), ESR1(2099), PGR(5241), SERPINA6(866), SHBG(6462) mouse ... Esr1(13982) rat ... Ar(24208), Esr1(24890), Nr3c1(24413), Nr3c2(25672), Pgr(25154)

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms	GHS02,GHS07,GHS08
signalword	Danger
hcodes	H225 - H315 - H332 - H360FD
pcodes	P202 - P210 - P233 - P303 + P361 + P353 - P304 + P340 + P312 - P308 + P313
Supp Hazards	EUH019
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN 2252 3 / PGII
WGK Germany	WGK 1
Flash Point F	41.0 °F - closed cup
Flash Point C	5 °C - closed cup

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Testosterone-d3 solution

CAS Number:	77546-39-5
EC Number:	203-794-9
MDL number:	MFCD00079586
PubChem Substance ID:	329826826
NACRES:	NA.24

1 mL in ampule

Quality Level	200
grade	analytical standard, for drug analysis
drug control	Home Office Schedule 4.2
concentration	100 µg/mL in 1,2-dimethoxyethane
application(s)	HPLC: suitable, gas chromatography (GC): suitable
format	single component solution
storage temp.	2-8°C
SMILES string	[H]C1([H])C[C@]2([H])[C@@]3([H])CCC4=CC(=O)CC[C@]4(C)[C@]3([H])CC[C@@]2(C)[C@]1([H])O
InChI	1S/C19H28O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h11,14-17,21H,3-10H2,1-2H3/t14-,15-,16-,17-,18-,19-/m0/s1/i6D2,17D
InChI key	MUMGGOZAMZWBJJ-HZRGXLBSSA-N

pictograms	GHS02,GHS07,GHS08
signalword	Danger
hcodes	H225 - H315 - H332 - H360FD
pcodes	P202 - P210 - P233 - P303 + P361 + P353 - P304 + P340 + P312 - P308 + P313
Supp Hazards	EUH019
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN 2252 3 / PGII
WGK Germany	WGK 1
Flash Point F	41.0 °F - closed cup
Flash Point C	5 °C - closed cup

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Tetrachloroethene solution 40083

CAS Number:

127-18-4

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	100
grade	certified reference material, TraceCERT^®
CofA	current certificate can be downloaded
packaging	ampule of 1 mL
concentration	5000 µg/mL in methanol
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Environmental Petroleum
format	single component solution
storage temp.	2-8°C
InChI	1S/C2Cl4/c3-1(4)2(5)6
InChI key	CYTYCFOTNPOANT-UHFFFAOYSA-N

Tetrachloroethene is a colorless liquid having an ethereal odor, which can find applications as a chemical intermediate and dry cleaning agent. It can also undergo reductive dehalogenation in the presence of an anaerobic bacterium to yield cis-1,2-dichloroethene.

pictograms	GHS02,GHS06,GHS08
signalword	Danger
hcodes	H225 - H301 + H311 + H331 - H370
pcodes	P210 - P233 - P280 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P311
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN1230 - class 3 - PG 2 - Methanol, solution
WGK Germany	WGK 2
Flash Point F	51.8 °F
Flash Point C	11 °C

202,36 € / 19 036 ₽

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Tetrachloroethene solution 48609

CAS Number:	127-18-4
EC Number:	200-659-6

General description

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	100
grade	certified reference material, TraceCERT^®
CofA	current certificate can be downloaded
packaging	ampule of 1 mL
concentration	200 µg/mL in methanol
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Environmental Petroleum
format	single component solution
InChI	1S/C2Cl4/c3-1(4)2(5)6
InChI key	CYTYCFOTNPOANT-UHFFFAOYSA-N

Tetrachloroethylene is a chlorinated ethylene compound commonly used as a dry cleaning and degreasing solvent. It is a groundwater contaminant, which has adverse effects on human health due to its potential toxicity and carcinogenicity.

pictograms	GHS02,GHS06,GHS08
signalword	Danger
hcodes	H225 - H301 + H311 + H331 - H370
pcodes	P210 - P233 - P280 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P311
RIDADR	UN1230 - class 3 - PG 2 - Methanol
WGK Germany	WGK 2
Flash Point F	51.8 °F - closed cup
Flash Point C	11 °C - closed cup

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Tetrachloroethylene

Empirical Formula (Hill Notation):	C₂Cl₄
Linear Formula:	CCl₂=CCl₂
CAS Number:	127-18-4
Molecular Weight:	165.83
Beilstein/REAXYS Number:	1361721
EC Number:	204-825-9
MDL number:	MFCD00000834
PubChem Substance ID:	329747481
NACRES:	NA.24

Tetrachloroethylene may be used as an extraction solvent for the determination of oils and grease in water samples using the Fourier-transform infrared spectroscopy technique. It may be used as an analytical reference standard for the quantification of the analyte in biological fluids using headspace solid-phase micro extraction-capillary gas chromatography with electron capture detection.

Quality Level	100
grade	analytical standard
vapor density	5.83 (vs air)
vapor pressure	13 mmHg ( 20 °C), 19 mmHg ( 25 °C)
assay	99.9% (GC)
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.505 (lit.), n20/D 1.506
bp	121 °C (lit.)
mp	22 °C (lit.)
density	1.623 g/mL at 25 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Environmental Food and Beverages Personal Care
format	neat
SMILES string	Cl\C(Cl)=C(\Cl)Cl
InChI	1S/C2Cl4/c3-1(4)2(5)6
InChI key	CYTYCFOTNPOANT-UHFFFAOYSA-N

Tetracycline hydrochloride is a broad-spectrum antibiotic, effective against both Gram-negative and Gram-positive microorganisms. Its aqueous solution has effective as a root canal irrigant for the removal of smear layer.
Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards.

pictograms	GHS07,GHS08,GHS09
signalword	Warning
hcodes	H315 - H317 - H319 - H336 - H351 - H411
pcodes	P202 - P273 - P280 - P302 + P352 - P305 + P351 + P338 - P308 + P313
Target Organs	Central nervous system
Personal Protective Equipment	Eyeshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN 1897 6.1 / PGIII
WGK Germany	WGK 3
Flash Point F	No data available
Flash Point C	No data available

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Tetracycline hydrochloride

Empirical Formula (Hill Notation):	C₂₂H₂₄N₂O₈ · HCl
CAS Number:	64-75-5
Molecular Weight:	480.90
Beilstein/REAXYS Number:	3844873
EC Number:	200-593-8
MDL number:	MFCD00078142
PubChem Substance ID:	329823071

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.
Tetracycline hydrochloride may be used as a pharmaceutical reference standard for the determination of the analyte in pharmaceutical formulations by kinetic spectrophotometric method.

Mode of Action: Tetracycline passively diffuses through proin channels in the cell membrane, binding to 30S ribosomes and inhibits protein synthesis by preventing access of aminoacyl tRNA to the acceptor site on the mRNA-ribosome complex. It also binds to the bacterial 50S ribosomal subunit, altering the membrane and causing intracellular components to leak from bacterial cells. The inhibitory effects can be reversed by washing, suggesting that it is the reversibly bound antibiotic, and not the irreversibly bound drug, that is responsible for antibacterial action.
Mode of Resistance: The effects are inactivated via a loss of cell wall permeability.
Antimicrobial spectrum: Includes a wide range of antimicrobial activity against gram-positive and gram-negative bacteria.

Caution

This product should be frozen below 0°C and protected from light and moisture. In these conditions, the product has been shown to retain activity for 4 years. Stock solutions should be stored at -20°C and are stable at 37°C for 4 days.

Preparation Note

The product is freely soluble in water, soluble in methanol and ethanol but is insoluble in ether and hydrocarbons. In water, the product yields a clear, yellow-orange solution with heating and in 95% ethanol, 50 mg dissolved in 4 mL with heating yields a clear, yellow-green solution. Tetracycline is rapidly destroyed by alkali hydroxide solutions and standing water solutions become turbid due to hydrolysis and precipitation. The potency of tetracycline is reduced in solutions with pH below 2.

Analysis Note

These secondary standards offer multi-traceability to the USP EP (PhEur) and BP primary standards where they are available.

To see an example of a Certificate of Analysis for this material enter LRAA7192 in the slot below. This is an example certificate only and may not be the lot that you receive.

Footnote

Quality Level	300
grade	certified reference material, pharmaceutical secondary standard
form	neat
CofA	current certificate can be downloaded
application(s)	HPLC: suitable, gas chromatography (GC): suitable
mp	220-223 °C (lit.)
Featured Industry	Pharmaceutical (small molecule)
format	neat
pharmacopeia traceability	traceable to BP 480, traceable to PhEur T060000, traceable to USP 1651009
SMILES string	Cl.CN(C)[C@H]1[C@@H]2C[C@H]3C(=C(O)[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)c4c(O)cccc4[C@@]3(C)O
InChI	1S/C22H24N2O8.ClH/c1-21(31)8-5-4-6-11(25)12(8)16(26)13-9(21)7-10-15(24(2)3)17(27)14(20(23)30)19(29)22(10,32)18(13)28;/h4-6,9-10,15,25,27-28,31-32H,7H2,1-3H3,(H2,23,30);1H/t9-,10-,15-,21+,22-;/m0./s1
InChI key	XMEVHPAGJVLHIG-FMZCEJRJSA-N

Tetrahydrocurcumin is a colorless compound and a major metabolite of curcumin, which is known to possess antioxidant activity and inhibitory effects on tertiary butyl hydroperoxide-induced lipid peroxidation. It can be obtained via hydrogenation of curcumin in the presence of platinum(IV)oxide.

pictograms	GHS08,GHS09
signalword	Warning
hcodes	H361d - H411
pcodes	P201 - P273 - P308 + P313
RIDADR	UN 3077 9 / PGIII
WGK Germany	WGK 2

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Tetrahydrocurcumin

Empirical Formula (Hill Notation):	C₂₁H₂₄O₆
CAS Number:	36062-04-1
Molecular Weight:	372.41
Beilstein/REAXYS Number:	3485469
MDL number:	MFCD04152347
PubChem Substance ID:	329757577
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Bottomless glass bottle. Contents are inside inserted fused cone.

grade	analytical standard
Quality Level	100
assay	≥95.0% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Food and Beverages
format	neat
SMILES string	COc1cc(CCC(=O)CC(=O)CCc2ccc(O)c(OC)c2)ccc1O
InChI	1S/C21H24O6/c1-26-20-11-14(5-9-18(20)24)3-7-16(22)13-17(23)8-4-15-6-10-19(25)21(12-15)27-2/h5-6,9-12,24-25H,3-4,7-8,13H2,1-2H3
InChI key	LBTVHXHERHESKG-UHFFFAOYSA-N

Tetrahydrofuran (THF) is a saturated cyclic ether. Its potential use as a biofuel for internal combustion engines is investigated.
Tetrahydrofuran is an important basic chemical compound, which belongs to the category of 5-membered heterocycles.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	385.2 °F
Flash Point C	196.2 °C

141,41 € / 13 302 ₽

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Tetrahydrofuran

Empirical Formula (Hill Notation):	C₄H₈O
CAS Number:	109-99-9
Molecular Weight:	72.11
Beilstein/REAXYS Number:	102391
EC Number:	203-726-8
MDL number:	MFCD00005356
PubChem Substance ID:	329768151
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Tetrahydrofuran may be used as an extraction solvent for the determination of pesticide residues in olive oil and phthalates in toys and child care articles by chromatography techniques.
Tetrahydrofuran may find application as a solvent in the synthesis of (S)-2-(1-pyrrolidinylmethyl)pyrrolidine. It is also an excellent solvent for sodium diisopropylamide, which can find applications as an effective base for the isomerization of alkenes and metalation of 1,4-dienes.

Quality Level	100
grade	analytical standard
vapor density	2.5 (vs air)
vapor pressure	114 mmHg ( 15 °C), 143 mmHg ( 20 °C)
assay	99.9% (GC)
form	neat
autoignition temp.	610 °F
shelf life	limited shelf life, expiry date on the label
contains	~0.025% 2,6-di-tert.-butyl-4-methylphenol as stabilizer
expl. lim.	1.8-11.8 %
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.407 (lit.)
bp	65-67 °C (lit.)
mp	108 °C (lit.)
solubility	H₂O: soluble
density	0.889 g/mL at 25 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Environmental Food and Beverages Personal Care
format	neat
SMILES string	C1CCOC1
InChI	1S/C4H8O/c1-2-4-5-3-1/h1-4H2
InChI key	WYURNTSHIVDZCO-UHFFFAOYSA-N

Tetramisole-d5 hydrochloride is an isotopically labeled compound of tetramisole.

pictograms	GHS02,GHS07,GHS08
signalword	Danger
hcodes	H225 - H302 - H319 - H335 - H336 - H351
pcodes	P201 - P202 - P210 - P301 + P312 - P305 + P351 + P338 - P308 + P313
Supp Hazards	EUH018 - EUH019
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN 2056 3 / PGII
WGK Germany	WGK 1
Flash Point F	-6.2 °F - closed cup
Flash Point C	-21.2 °C - closed cup

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Tetramisole-d5 hydrochloride

Empirical Formula (Hill Notation):	C₁₁D₅H₇N₂S · HCl
CAS Number:	1173021-85-6
Molecular Weight:	245.78
MDL number:	MFCD16661171
PubChem Substance ID:	329754357
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Tetramisole-d5 hydrochloride may be used as an internal standard for the determination of levamisole in milk samples by liquid chromatography-tandem mass spectrometry (LC-MS/MS).

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	100
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
mass shift	M+5
SMILES string	Cl.[2H]c1c([2H])c([2H])c(c([2H])c1[2H])C2CN3CCSC3=N2
InChI	1S/C11H12N2S.ClH/c1-2-4-9(5-3-1)10-8-13-6-7-14-11(13)12-10;/h1-5,10H,6-8H2;1H/i1D,2D,3D,4D,5D;
InChI key	LAZPBGZRMVRFKY-GWVWGMRQSA-N

Tetrandrine (TET) is classified under the bisbenzylisoquinoline alkaloid family of compounds extracted from Stephania tetrandra S. Moore.

pictograms	GHS07
signalword	Warning
hcodes	H302 - H315 - H319 - H335
pcodes	P261 - P264 - P270 - P301 + P312 - P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Tetrandrine

Empirical Formula (Hill Notation):	C₃₈H₄₂N₂O₆
CAS Number:	518-34-3
Molecular Weight:	622.75
MDL number:	MFCD08689909
PubChem Substance ID:	329826723
NACRES:	NA.24

Analgesic, antipyretic.
TET may be used as an analytical reference standard for the determination of TET in:

Blood samples by online multidimensional solid phase extraction liquid chromatography coupled to tandem mass spectrometry (MD-SPE-LC-MS/MS) equipped with electrospray ionization (ESI) source and multiple reaction monitoring (MRM) detection.
Rat plasma by ultra-high performance liquid chromatography (UHPLC) combined with MS/MS with MRM detection.
Qi-Fang-Xi-Bi-Granules used in Chinese medicine by reversed phase HPLC equipped with ultraviolet (UV) detector.
Fangji Huangqi Tang Chinese medicine by UHPLC coupled to triple quadrupole mass spectrometry (QqQ-MS) with MRM detection.

It may be used as an internal standard for the determination of hernandezine in:

Rat plasma and tissues by UHPLC-MS/MS with MRM detection.

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

1 g in poly bottle

Quality Level	100
grade	analytical standard, for drug analysis
assay	90%
form	solid
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	COc1ccc2C[C@@H]3N(C)CCc4cc(OC)c(OC)c(Oc5cc6[C@H](Cc7ccc(Oc1c2)cc7)N(C)CCc6cc5OC)c34
InChI	1S/C38H42N2O6/c1-39-15-13-25-20-32(42-4)34-22-28(25)29(39)17-23-7-10-27(11-8-23)45-33-19-24(9-12-31(33)41-3)18-30-36-26(14-16-40(30)2)21-35(43-5)37(44-6)38(36)46-34/h7-12,19-22,29-30H,13-18H2,1-6H3/t29-,30-/m0/s1
InChI key	WVTKBKWTSCPRNU-KYJUHHDHSA-N

Theaflavin is a polyphenol, naturally available in tea, which can mainly play a role in the inhibition of xanthine oxidase enzyme to yield uric acid. It can also find applications in reducing oxidative stress and can also act like scavengers of superoxide.

pictograms	GHS06
signalword	Danger
hcodes	H300
pcodes	P264 - P270 - P301 + P310 - P405 - P501
Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Theaflavin

Empirical Formula (Hill Notation):	C₂₉H₂₄O₁₂
CAS Number:	4670-05-7
Molecular Weight:	564.49
MDL number:	MFCD03427500
PubChem Substance ID:	329758072
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Bottomless glass bottle. Contents are inside inserted fused cone.

grade	analytical standard
Quality Level	100
assay	≥90.0% (HPLC)
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Food and Beverages
format	neat
storage temp.	−20°C
SMILES string	O[C@@H]1Cc2c(O)cc(O)cc2O[C@@H]1C3=Cc4c(cc(O)c(O)c4C(=O)C(O)=C3)[C@H]5Oc6cc(O)cc(O)c6C[C@H]5O
InChI	1S/C29H24O12/c30-11-3-17(32)15-8-21(36)28(40-23(15)5-11)10-1-13-14(7-20(35)27(39)25(13)26(38)19(34)2-10)29-22(37)9-16-18(33)4-12(31)6-24(16)41-29/h1-7,21-22,28-33,35-37,39H,8-9H2,(H,34,38)/t21-,22-,28-,29-/m1/s1
InChI key	IPMYMEWFZKHGAX-ZKSIBHASSA-N

Chemical structure: sulfonamide
Thiamphenicol is an analog of a broad spectrum antibiotic, chloramphenicol. It shows therapeutic effects in respiratory infections, venereal diseases and bacterial prostatitis.

Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Thiamphenicol

Empirical Formula (Hill Notation):	C₁₂H₁₅Cl₂NO₅S
CAS Number:	15318-45-3
Molecular Weight:	356.22
Beilstein/REAXYS Number:	2819542
EC Number:	239-355-3
MDL number:	MFCD00467983
PubChem Substance ID:	329751348
NACRES:	NA.24

Thiamphenicol may be used as a reference standard in the determination of thiamphenicol in honey using dispersive liquid-liquid microextraction (DLLME) coupled with high-performance liquid chromatography-variable wavelength detector (HPLC-VWD).
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Quality Level	100
grade	analytical standard
assay	≥99.0% (HPLC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
solubility	ethanol: 50 mg/mL, clear, colorless to faintly yellow
Featured Industry	Clinical
format	neat
storage temp.	2-8°C
SMILES string	CS(=O)(=O)c1ccc(cc1)[C@@H](O)[C@@H](CO)NC(=O)C(Cl)Cl
InChI	1S/C12H15Cl2NO5S/c1-21(19,20)8-4-2-7(3-5-8)10(17)9(6-16)15-12(18)11(13)14/h2-5,9-11,16-17H,6H2,1H3,(H,15,18)/t9-,10-/m1/s1
InChI key	OTVAEFIXJLOWRX-NXEZZACHSA-N

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 2
Flash Point F	Not applicable
Flash Point C	Not applicable

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Thiamylal

Empirical Formula (Hill Notation):	C₁₂H₁₈N₂O₂S
CAS Number:	77-27-0
Molecular Weight:	254.35
EC Number:	201-018-3
MDL number:	MFCD00057565
PubChem Substance ID:	329826909
NACRES:	NA.24

Intravenous anesthetic

grade	analytical standard
Quality Level	200
form	neat
drug control	USDEA Schedule III; regulated under CDSA - not available from Sigma-Aldrich Canada
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	S=C(N1)NC(C(C(C)CCC)(CC=C)C1=O)=O
InChI	1S/C12H18N2O2S/c1-4-6-8(3)12(7-5-2)9(15)13-11(17)14-10(12)16/h5,8H,2,4,6-7H2,1,3H3,(H2,13,14,15,16,17)
InChI key	XLOMZPUITCYLMJ-UHFFFAOYSA-N
Gene Information	human ... GABRA1(2554), GABRA2(2555), GABRA3(2556), GABRA4(2557), GABRA5(2558), GABRA6(2559), GABRB1(2560), GABRB2(2561), GABRB3(2562), GABRD(2563), GABRE(2564), GABRG1(2565), GABRG2(2566), GABRG3(2567), GABRP(2568), GABRQ(55879)

Thiophene belongs to the class of polycyclic aromatic sulfur heterocycles, which are carcinogenic compounds found in crude oil. Thiopenes are widely used as building blocks in many agrochemicals, pharmaceuticals, and material science.

pictograms	GHS06
signalword	Danger
hcodes	H301 + H311 + H331
pcodes	P261 - P264 - P280 - P301 + P310 - P302 + P352 + P312 - P304 + P340 + P311
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
RIDADR	UN 2811 6.1 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Thiophene

Empirical Formula (Hill Notation):	C₄H₄S
CAS Number:	110-02-1
Molecular Weight:	84.14
Beilstein/REAXYS Number:	103222
EC Number:	203-729-4
MDL number:	MFCD00005413
PubChem Substance ID:	329748301
NACRES:	NA.24

Thiophene may be used as an analytical reference standard for the quantification of the analyte in diesel oil and crude oil using two-dimensional gas chromatography with sulfur chemiluminescence detection.

Quality Level	100
grade	analytical standard
vapor density	2.9 (vs air)
vapor pressure	40 mmHg ( 12.5 °C)
assay	99.5% (GC)
autoignition temp.	743 °F
shelf life	limited shelf life, expiry date on the label
expl. lim.	12.5 %
application(s)	HPLC: suitable, gas chromatography (GC): suitable
impurities	~0.2% benzene
refractive index	n20/D 1.529 (lit.), n20/D 1.529
bp	84 °C (lit.)
mp	38 °C (lit.)
density	1.051 g/mL at 25 °C (lit.)
Featured Industry	Environmental
format	neat
SMILES string	c1ccsc1
InChI	1S/C4H4S/c1-2-4-5-3-1/h1-4H
InChI key	YTPLMLYBLZKORZ-UHFFFAOYSA-N

Thiophenol is an organosulfur compound, which is used as a raw material for the syntheses of pesticides, polymers, and pharmaceuticals.

pictograms	GHS02,GHS07,GHS08
signalword	Danger
hcodes	H225 - H302 - H319 - H340 - H350 - H412
pcodes	P202 - P210 - P273 - P301 + P312 - P305 + P351 + P338 - P308 + P313
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN 2414 3 / PGII
WGK Germany	WGK 3
Flash Point F	15.8 °F
Flash Point C	-9 °C

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Thiophenol

Empirical Formula (Hill Notation):	C₆H₆S
Linear Formula:	C₆H₅SH
CAS Number:	108-98-5
Molecular Weight:	110.18
Beilstein/REAXYS Number:	506523
EC Number:	203-635-3
MDL number:	MFCD00004826
PubChem Substance ID:	329748755
NACRES:	NA.24

Thiophenol may be used as an analytical reference standard for the quantification of the analyte in water samples using chromatography techniques.

PESTANAL is a registered trademark of Sigma-Aldrich International GmbH

Quality Level	100
grade	analytical standard
vapor density	3.8 (vs air)
vapor pressure	1.4 mmHg ( 20 °C)
product line	PESTANAL^®
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.588 (lit.)
bp	169 °C (lit.)
mp	15 °C (lit.)
density	1.073 g/mL at 25 °C (lit.)
Featured Industry	Agriculture Cleaning Products Cosmetics Environmental Flavors and Fragrances Food and Beverages Personal Care
format	neat
SMILES string	Sc1ccccc1
InChI	1S/C6H6S/c7-6-4-2-1-3-5-6/h1-5,7H
InChI key	RMVRSNDYEFQCLF-UHFFFAOYSA-N

pictograms	GHS02,GHS06,GHS08,GHS09
signalword	Danger
hcodes	H226 - H300 + H310 + H330 - H315 - H319 - H335 - H361 - H372 - H410
pcodes	P210 - P273 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
Target Organs	Kidney, Respiratory system
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
RIDADR	UN 2337 3(6.1) / PGI
WGK Germany	WGK 3
Flash Point F	122.0 °F - closed cup
Flash Point C	50 °C - closed cup

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Thujone Standard Mixture

Empirical Formula (Hill Notation):	C₁₀H₁₆O
CAS Number:	76231-76-0
Molecular Weight:	152.23
MDL number:	MFCD00135597
NACRES:	NA.24

Quality Level	100
grade	analytical standard
description	reference substance for GC
composition	-thujone, 90-98% , -thujone, 2-10%
application(s)	HPLC: suitable, gas chromatography (GC): suitable
refractive index	n20/D 1.450, n20/D 1.455 (lit.)
bp	84-86 °C/17 mmHg (lit.)
density	0.925 g/mL at 25 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Flavors and Fragrances Food and Beverages Personal Care
format	neat
storage temp.	2-8°C
SMILES string	CC(C)[C@@]12C[C@@H]1[C@@H](C)C(=O)C2.CC(C)[C@@]34C[C@@H]3[C@H](C)C(=O)C4
InChI	1S/2C10H16O/c21-6(2)10-4-8(10)7(3)9(11)5-10/h26-8H,4-5H2,1-3H3/t7-,8+,10-;7-,8-,10+/m01/s1
InChI key	AKPBIVZAUPVDMO-APEKEWONSA-N

Thymol is a phenol compound and a major component of essential oil extracted from Thymus vulgaris L. medicinal plant. It exhibits antioxidant and antimicrobial properties and is widely used to treat bronchitis, gastritis, laryngitis, indigestion and dry coughs.

pictograms	GHS07
signalword	Warning
hcodes	H302
pcodes	P264 - P270 - P301 + P312 - P501
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
WGK Germany	WGK 3
Flash Point F	152.6 °F - closed cup
Flash Point C	67 °C - closed cup

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Thymol

Empirical Formula (Hill Notation):	C₁₀H₁₄O
Linear Formula:	2-[(CH₃)₂CH]C₆H₃-5-(CH₃)OH
CAS Number:	89-83-8
Molecular Weight:	150.22
Beilstein/REAXYS Number:	1907135
EC Number:	201-944-8
MDL number:	MFCD00002309
PubChem Substance ID:	329764107

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Thymol may be used as an analytical reference standard for the quantification of the analyte in Thymus vulgaris L. volatile oil using high-performance liquid chromatography technique.

Bottomless glass bottle. Contents are inside inserted fused cone.

Quality Level	100
grade	analytical standard
vapor pressure	1 mmHg ( 64 °C)
assay	99.9% (GC)
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
bp	232 °C (lit.)
mp	48-51 °C (lit.), 49-51 °C
density	0.965 g/mL at 25 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Environmental Flavors and Fragrances Food and Beverages Personal Care
format	neat
SMILES string	CC(C)c1ccc(C)cc1O
InChI	1S/C10H14O/c1-7(2)9-5-4-8(3)6-10(9)11/h4-7,11H,1-3H3
InChI key	MGSRCZKZVOBKFT-UHFFFAOYSA-N

Thymoquinone is employed in preclinical studies as neuroprotective and anticonvulsant agent.

pictograms	GHS05,GHS07,GHS09
signalword	Danger
hcodes	H302 - H314 - H411
pcodes	P260 - P273 - P280 - P301 + P312 - P303 + P361 + P353 - P305 + P351 + P338
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type P1 (EN143) respirator filter, type P3 (EN 143) respirator cartridges
RIDADR	UN2430 - class 8 - PG 3 - EHS - Alkylphenols, solid, n.o.s., HI: A,S
WGK Germany	WGK 2
Flash Point F	240.8 °F - closed cup
Flash Point C	116 °C - closed cup

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Thymoquinone

Empirical Formula (Hill Notation):	C₁₀H₁₂O₂
CAS Number:	490-91-5
Molecular Weight:	164.20
EC Number:	207-721-1
MDL number:	MFCD00001602
PubChem Substance ID:	329747625
NACRES:	NA.24

Thymoquinone has been used as an analytical standard for the determination of thymoquinone in Nigella sativa extracts and formulations by high performance thin layer chromatography (HPTLC). It may be used as a reference standard for the identification of thymoquinone as volatile aglycone in seasonally collected Satureja montana L. and in Juniperus oxycedrus L. by gas chromatography-mass spectrometry (GC-MS).

Quality Level	100
grade	analytical standard
assay	98.5% (GC)
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
bp	230-232 °C (lit.)
mp	45-47 °C (lit.)
Featured Industry	Cleaning Products Cosmetics Flavors and Fragrances Food and Beverages Personal Care
format	neat
SMILES string	CC(C)C1=CC(=O)C(C)=CC1=O
InChI	1S/C10H12O2/c1-6(2)8-5-9(11)7(3)4-10(8)12/h4-6H,1-3H3
InChI key	KEQHJBNSCLWCAE-UHFFFAOYSA-N

Sigma-Aldrich offers tiamulin fumarate for a variety of applications that include, but are not limited to, environmental, food and beverage, forensics, petrochemical and pharmaceutical analyses. Purity of the chemical is about 99% unless otherwise stated.

pictograms	GHS07
signalword	Warning
hcodes	H302 - H315 - H319 - H335
pcodes	P301 + P312 + P330 - P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	219.2 °F - closed cup
Flash Point C	104 °C - closed cup

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Tiamulin fumarate

Empirical Formula (Hill Notation):	C₃₂H₅₁NO₈S
CAS Number:	55297-96-6
Molecular Weight:	609.81
EC Number:	259-581-6
MDL number:	MFCD00145407
PubChem Substance ID:	329757276
NACRES:	NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

Quality Level	100
grade	analytical standard
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Clinical Forensics and Toxicology Pharmaceutical (small molecule)
format	neat
storage temp.	2-8°C
SMILES string	OC(=O)\C=C\C(O)=O.CCN(CC)CCSCC(=O)O[C@@H]1C[C@@](C)(C=C)[C@@H](O)[C@H](C)[C@@]23CC[C@@H](C)[C@]1(C)[C@@H]2C(=O)CC3
InChI	1S/C28H47NO4S.C4H4O4/c1-8-26(6)17-22(33-23(31)18-34-16-15-29(9-2)10-3)27(7)19(4)11-13-28(20(5)25(26)32)14-12-21(30)24(27)28;5-3(6)1-2-4(7)8/h8,19-20,22,24-25,32H,1,9-18H2,2-7H3;1-2H,(H,5,6)(H,7,8)/b;2-1+/t19?,20-,22+,24-,25-,26+,27-,28-;/m0./s1
InChI key	YXQXDXAHCSEVSD-IHAONTCTSA-N

Ticlopidine hydrochloride has been used as an analytical standard to investigate the developmental toxicity and teratogenic potential of ticlopidine in Xenopus laevis embryos and human endothelial cells using a frog embryo teratogenesis assay-Xenopus (FETAX) and blood and lymph vessel formation assay.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms	GHS07
signalword	Warning
hcodes	H302
pcodes	P264 - P270 - P301 + P312 - P501
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	UN 2811 6.1 / PGIII
WGK Germany	WGK 3

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Ticlopidine hydrochloride

Empirical Formula (Hill Notation):	C₁₄H₁₄ClNS · HCl
CAS Number:	53885-35-1
Molecular Weight:	300.25
EC Number:	258-837-4
MDL number:	MFCD00079606
PubChem Substance ID:	329826850
NACRES:	NA.24

Quality Level	100
grade	analytical standard, for drug analysis
assay	99%
form	neat
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Forensics and Toxicology Pharmaceutical (small molecule) Veterinary
format	neat
SMILES string	Cl.Clc1ccccc1CN2CCc3sccc3C2
InChI	1S/C14H14ClNS.ClH/c15-13-4-2-1-3-11(13)9-16-7-5-14-12(10-16)6-8-17-14;/h1-4,6,8H,5,7,9-10H2;1H
InChI key	MTKNGOHFNXIVOS-UHFFFAOYSA-N
Gene Information	human ... P2RY12(64805)

Tilmicosin is a semisynthetic macrolide antibiotic, with broad spectrum activity towards Mycoplasma spp., Pasteurella spp., and various gram-positive organisms in animals.

pictograms	GHS07
signalword	Warning
hcodes	H302
pcodes	P301 + P312 + P330
Personal Protective Equipment	dust mask type N95 (US), Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Tilmicosin

Empirical Formula (Hill Notation):	C₄₆H₈₀N₂O₁₃
Molecular Weight:	869.13
MDL number:	MFCD19705582
PubChem Substance ID:	329754677
NACRES:	NA.24

Commission Regulation (EU) No 37/2010 of 22 December 2009 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Tilmicosin may be used as a reference standard for the determination of the analyte in chicken, swine, cattle, sheep tissues and milk samples using liquid chromatography with ultraviolet detection (LC-UV).

VETRANAL is a registered trademark of Sigma-Aldrich Chemie GmbH

grade	analytical standard
Quality Level	100
product line	VETRANAL^®
form	neat
shelf life	limited shelf life, expiry date on the label
application(s)	HPLC: suitable
Featured Industry	Pharmaceutical (small molecule)
format	neat
SMILES string	CC1OC(OCC(C(CC)O2)/C=C(/C=C/C(C(C)CC(CCN3CC(C)CC(C)C3)C(OC4OC(C)C(O)C(N(C)C)C4O)C(C)C(O)CC2=O)=O)C)C(OC)C(OC)C1O
InChI	1S/C46H80N2O13/c1-13-36-33(24-57-46-44(56-12)43(55-11)40(53)31(8)59-46)19-25(2)14-15-34(49)28(5)20-32(16-17-48-22-26(3)18-27(4)23-48)42(29(6)35(50)21-37(51)60-36)61-45-41(54)38(47(9)10)39(52)30(7)58-45/h14-15,19,26-33,35-36,38-46,50,52-54H,13,16-18,20-24H2,1-12H3/b15-14+,25-19+/t26-,27+,28-,29+,30-,31-,32+,33-,35-,36-,38+,39-,40-,41-,42-,43-,44-,45+,46-/m1/s1
InChI key	JTSDBFGMPLKDCD-XVFHVFLVSA-N

Personal Protective Equipment	Eyeshields, Gloves, type N95 (US)
RIDADR	NONH for all modes of transport
WGK Germany	WGK 3

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TO11/IP-6A Aldehyde/Ketone-DNPH Mix CRM47285

NACRES:

NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	100
grade	certified reference material, TraceCERT^®
CofA	current certificate can be downloaded
packaging	ampule of 1 mL
concentration	15 µg/mL in acetonitrile (as the aldehyde)
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Environmental
format	multi-component solution
storage temp.	2-8°C

pictograms	GHS02,GHS07
signalword	Danger
hcodes	H225 - H302 + H312 + H332 - H319
pcodes	P210 - P280 - P301 + P312 - P303 + P361 + P353 - P304 + P340 + P312 - P305 + P351 + P338
RIDADR	UN 1648 3 / PGII
WGK Germany	WGK 2
Flash Point F	35.6 °F - closed cup
Flash Point C	2.0 °C - closed cup

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TO11/IP-6A Aldehyde/Ketone-DNPH Mix CRM4M7285

NACRES:

NA.24

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
TO11/IP-6A Aldehyde/Ketone-DNPH Mix has been used as certified reference material:

For the determination of air-dispersed formaldehyde and carbonyl compounds (CCs) as vapors by denuder-filter sampling and gas chromatography method of analysis.
To investigate the impact of NO, NO2 and CO in air samples on the capture and retention of formaldehyde and acetaldehyde with the DNPH-cartridge. The reaction products and chromatographic interferences are identified using chromatography techniques.

TraceCERT is a registered trademark of Sigma-Aldrich Co. LLC

Quality Level	100
grade	certified reference material, TraceCERT^®
CofA	current certificate can be downloaded
packaging	ampule of 3 x 1 mL
concentration	15 µg/mL each component in acetonitrile (as the aldehyde or ketone)
application(s)	HPLC: suitable, gas chromatography (GC): suitable
Featured Industry	Environmental
format	multi-component solution
storage temp.	2-8°C