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(+)-Pseudoephedrine hydrochloride
Empirical Formula (Hill Notation): C10H15NO · HCl Linear Formula: C6H5CH[CH(NHCH3)CH3]OH·HCl CAS Number: 345-78-8 Molecular Weight: 201.69 Beilstein/REAXYS Number: 3915112 EC Number: 206-462-1 MDL number: MFCD00058088 PubChem Substance ID: 24894482 NACRES: NA.77
Кат. номер E2750-100G E2750-25G E2750-1G Packaging25, 100 g in glass bottleBiochem/physiol ActionsNon-selective adrenergic agonist; decongestantПараметрыQuality Level 200 assay 98% application(s) HPLC: suitable, gas chromatography (GC): suitable mp 185-188 °C (lit.) Featured Industry Forensics and Toxicology
Pharmaceutical (small molecule)
VeterinarySMILES string Cl.CN[C@@H](C)[C@@H](O)c1ccccc1 InChI 1S/C10H15NO.ClH/c1-8(11-2)10(12)9-6-4-3-5-7-9;/h3-8,10-12H,1-2H3;1H/t8-,10+;/m0./s1 InChI key BALXUFOVQVENIU-KXNXZCPBSA-N
Safety Informationpictograms GHS07 signalword Warning hcodes H302 - H336 pcodes P301 + P312 + P330 Target Organs Central nervous system Personal Protective Equipment dust mask type N95 (US), Eyeshields, Faceshields, Gloves RIDADR NONH for all modes of transport WGK Germany WGK 3 Узнать цену -
(Z)-Guggulsterone
Empirical Formula (Hill Notation): C21H28O2 CAS Number: 39025-23-5 Molecular Weight: 312.45 MDL number: MFCD01310757 PubChem Substance ID: 24278392 NACRES: NA.77
Кат. номер G5168-25MG-PW G5168-5MG G5168-25MG G5168-5MG-PW Biochem/physiol Actions(Z)-Guggulsterone is a natural product that lowers cholesterol due to its function as an antagonist ligand for the bile acid receptor. (Z)-Guggulsterone is a nuclear hormone receptor that regulates the transcription of several genes involved in cholesterol metabolism and plays a role in cholesterol level regulation. (Z)-Guggulsterone is also a selective farnesoid X receptor (FXR) modulator.ПараметрыQuality Level 200 assay 89% (HPLC) form powder application(s) HPLC: suitable, gas chromatography (GC): suitable impurities 5.4% E-form color light yellow solubility DMSO: 5 mg/mL Featured Industry Forensics and Toxicology
Veterinarystorage temp. 2-8°C SMILES string [H][C@@]12CCC3=CC(=O)CC[C@]3(C)[C@@]1([H])CC[C@]4(C)\C(=C\C)C(=O)C[C@@]24[H] InChI 1S/C21H28O2/c1-4-16-19(23)12-18-15-6-5-13-11-14(22)7-9-20(13,2)17(15)8-10-21(16,18)3/h4,11,15,17-18H,5-10,12H2,1-3H3/b16-4+/t15-,17+,18+,20+,21-/m1/s1 InChI key WDXRGPWQVHZTQJ-OSJVMJFVSA-N
Safety Informationpictograms GHS07 signalword Warning hcodes H315 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 Узнать цену -
-Estradiol
Empirical Formula (Hill Notation): C18H24O2 CAS Number: 50-28-2 Molecular Weight: 272.38 Beilstein/REAXYS Number: 1914275 EC Number: 200-023-8 MDL number: MFCD00003693 PubChem Substance ID: 24894389 NACRES: NA.77
Кат. номер E1132-5VL E1132-1VL Packaging1 vial in poly bottle
Supplied in amber screw-cap vialsBiochem/physiol ActionsThe major estrogen secreted by the premenopausal ovary. Estrogens direct the development of the female phenotype in embryogenesis and during puberty by regulating gene transcription and, thus, protein synthesis. It also induces the production of gonadotropins which, in turn, induce ovulation. Exposure to estradiol increases breast cancer incidence and proliferation.Параметрыgrade analytical standard Quality Level 200 packaging vial of 250 mg application(s) HPLC: suitable, gas chromatography (GC): suitable mp 176-180 °C (lit.) Featured Industry Pharmaceutical SMILES string O[C@H]1CC[C@@]2([H])[C@]3([H])CCC4=CC(O)=CC=C4[C@@]3([H])CC[C@@]21C InChI 1S/C18H24O2/c1-18-9-8-14-13-5-3-12(19)10-11(13)2-4-15(14)16(18)6-7-17(18)20/h3,5,10,14-17,19-20H,2,4,6-9H2,1H3/t14-,15-,16+,17+,18+/m1/s1 InChI key VOXZDWNPVJITMN-ZBRFXRBCSA-N Gene Information human ... ESR1(2099), ESR2(2100), ESRRA(2101), ESRRB(2103), GPER(2852), SERPINA6(866)
mouse ... Esr1(13982), Esr2(13983), Esrra(26379)
rat ... Afp(24177), Ar(24208), Esr1(24890), Esr2(25149), Shbg(24775)
Safety Informationpictograms GHS08,GHS09 signalword Danger hcodes H351 - H360FD - H362 - H410 pcodes P202 - P260 - P263 - P264 - P273 - P308 + P313 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 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Acetylsalicylic acid
Empirical Formula (Hill Notation): C9H8O4 Linear Formula: 2-(CH3CO2)C6H4CO2H CAS Number: 50-78-2 Molecular Weight: 180.16 Beilstein/REAXYS Number: 779271 EC Number: 200-064-1 MDL number: MFCD00002430 PubChem Substance ID: 24890723 NACRES: NA.21
Кат. номер A3160-5X1VL A3160-1VL Packaging1 vial in poly bottle
Supplied in amber screw-cap vialsBiochem/physiol ActionsBlocks the production of prostaglandins by inhibiting cyclooxygenase (prostaglandin H synthase), with greater selectivity toward the COX-1 isoform. The antithrombotic effect is due to the inhibition of COX-1 in platelets that blocks thromboxane production and platelet aggregation. Chemopreventive against colorectal and other solid tumors.ПараметрыQuality Level 200 grade analytical standard form powder packaging vial of 500 mg application(s) HPLC: suitable, gas chromatography (GC): suitable mp 134-136 °C (lit.) Featured Industry Forensics and Toxicology
Pharmaceutical
VeterinarySMILES string CC(=O)Oc1ccccc1C(O)=O InChI 1S/C9H8O4/c1-6(10)13-8-5-3-2-4-7(8)9(11)12/h2-5H,1H3,(H,11,12) InChI key BSYNRYMUTXBXSQ-UHFFFAOYSA-N Gene Information human ... ITGA2B(3674), PTGS1(5742), PTGS2(5743)
Safety Informationpictograms GHS07 signalword Warning hcodes H302 pcodes P301 + P312 + P330 Personal Protective Equipment dust mask type N95 (US), Eyeshields, Faceshields, Gloves RIDADR NONH for all modes of transport WGK Germany WGK 1 Flash Point F 482.0 °F Flash Point C 250 °C Узнать цену -
AH 11110
Empirical Formula (Hill Notation): C21H26N2O2 · HCl CAS Number: 179388-65-9 Molecular Weight: 374.90 MDL number: MFCD03093187 PubChem Substance ID: 24890774 NACRES: NA.77
Кат. номер A3477-50MG A3477-10MG Packaging50 mg in poly bottleBiochem/physiol Actions1B-adrenoceptor ligandFeatures and BenefitsThis compound was developed by GlaxoSmithKline. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.ПараметрыQuality Level 100 assay >98% (HPLC) form solid application(s) HPLC: suitable, gas chromatography (GC): suitable color slightly yellow solubility H2O: soluble ~2.5 mg/mL, DMSO: insoluble Featured Industry Forensics and Toxicology
Veterinaryoriginator GlaxoSmithKline storage temp. 20°C SMILES string Cl[H].OC(COc1ccccc1-c2ccccc2)CC(=N)N3CCCCC3 InChI 1S/C21H26N2O2.ClH/c22-21(23-13-7-2-8-14-23)15-18(24)16-25-20-12-6-5-11-19(20)17-9-3-1-4-10-17;/h1,3-6,9-12,18,22,24H,2,7-8,13-16H2;1H InChI key WWHGFIXWBLHHQB-UHFFFAOYSA-N
Safety InformationPersonal 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 Узнать цену -
Anisotropine methyl bromide
Empirical Formula (Hill Notation): C17H32BrNO2 CAS Number: 80-50-2 Molecular Weight: 362.35 EC Number: 201-285-6 MDL number: MFCD00083234 PubChem Substance ID: 24890953 NACRES: NA.22
Кат. номер A5181-5G A5181-1G A5181-25G ПараметрыQuality Level 200 application(s) HPLC: suitable, gas chromatography (GC): suitable Featured Industry Forensics and Toxicology
Veterinarystorage temp. 2-8°C SMILES string [Br-].CCCC(CCC)C(=O)O[C@H]1C[C@H]2CC[C@@H](C1)[N+]2(C)C InChI 1S/C17H32NO2.BrH/c1-5-7-13(8-6-2)17(19)20-16-11-14-9-10-15(12-16)18(14,3)4;/h13-16H,5-12H2,1-4H3;1H/q+1;/p-1/t14-,15+,16+; InChI key QSFKGMJOKUZAJM-CNKDKAJDSA-M Gene Information human ... CHRM1(1128), CHRM3(1131)
Safety Informationpictograms GHS07,GHS09 signalword Warning hcodes H302 + H312 + H332 - H400 pcodes P273 - P280 - P301 + P312 + P330 - P302 + P352 + P312 - P304 + P340 + P312 Personal Protective Equipment dust mask type N95 (US), Eyeshields, Gloves RIDADR UN 3077 9 / PGIII WGK Germany WGK 3 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Fluoxymesterone
Empirical Formula (Hill Notation): C20H29FO3 CAS Number: 76-43-7 Molecular Weight: 336.44 EC Number: 200-961-8 MDL number: MFCD00010480 PubChem Substance ID: 24894947
Кат. номер F7751-100MG F7751-50MG F7751-5G F7751-500MG F7751-1G Biochem/physiol ActionsFluoxymesterone is an androgen and anabolic steroid.Параметрыbiological source Porcine pancreas, bovine milk (other parts like skeletal muscle/bile/bone/connective tissue/skin), microbial (Mycobacterium sp.) form solid (photosensitive) drug control USDEA Schedule III; Home Office Schedule 4.2; regulated under CDSA - not available from Sigma-Aldrich Canada application(s) HPLC: suitable, gas chromatography (GC): suitable color white solubility H2O: 0.5 mg/mL, 45% (w/v) aq 2-hydroxypropyl--cyclodextrin: 6.4 mg/mL, ethanol: 7.3 mg/mL Featured Industry Forensics and Toxicology
Veterinaryshipped in ambient storage temp. room temp SMILES string [H][C@@]12CC[C@](C)(O)[C@@]1(C)C[C@H](O)[C@@]3(F)[C@@]2([H])CCC4=CC(=O)CC[C@]34C InChI 1S/C20H29FO3/c1-17-8-6-13(22)10-12(17)4-5-15-14-7-9-19(3,24)18(14,2)11-16(23)20(15,17)21/h10,14-16,23-24H,4-9,11H2,1-3H3/t14-,15-,16-,17-,18-,19-,20-/m0/s1 InChI key YLRFCQOZQXIBAB-RBZZARIASA-N Gene Information human ... AR(367), ESR1(2099), PRLR(5618)
Safety Informationpictograms GHS08 signalword Warning hcodes H361 pcodes P281 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 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Formestane F2552-1G
Empirical Formula (Hill Notation): C19H26O3 CAS Number: 566-48-3 Molecular Weight: 302.41 MDL number: MFCD00057814 PubChem Substance ID: 24894827 NACRES: NA.25 Packaging1 g in glass bottleBiochem/physiol ActionsAromatase inhibitor used as an anti-cancer agent against estrogen-dependent tumors.Параметрыbiological source synthetic (organic) Quality Level 100 assay 98% (HPLC) form solid application(s) HPLC: suitable, gas chromatography (GC): suitable solubility chloroform: 50 mg/mL, clear to slightly hazy, colorless to faintly yellow Featured Industry Forensics and Toxicology
Veterinarystorage temp. 2-8°C SMILES string C[C@]12CC[C@H]3[C@@H](CCC4=C(O)C(=O)CC[C@]34C)[C@@H]1CCC2=O InChI 1S/C19H26O3/c1-18-10-8-15(20)17(22)14(18)4-3-11-12-5-6-16(21)19(12,2)9-7-13(11)18/h11-13,22H,3-10H2,1-2H3/t11-,12-,13-,18+,19-/m0/s1 InChI key OSVMTWJCGUFAOD-KZQROQTASA-N Gene Information human ... CYP19A1(1588)
Safety Informationpictograms GHS08 signalword Danger hcodes H360 pcodes P201 - P308 + P313 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 Узнать цену -
Hydrocodone (+)-bitartrate salt
Empirical Formula (Hill Notation): C18H21NO3 · C4H6O6 CAS Number: 143-71-5 Molecular Weight: 449.45 EC Number: 205-608-1 MDL number: MFCD00078557 PubChem Substance ID: 24895519 NACRES: NA.77
Кат. номер H4516-10MG H4516-50MG H4516-250MG Biochem/physiol Actionsμ opioid receptor agonist; narcotic analgesic and antitussive.Features and BenefitsThis compound was developed by Abbott. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.ПараметрыQuality Level 200 drug control USDEA Schedule II; Home Office Schedule 2; stupfiant (France); kontrollierte Droge in Deutschland; regulated under CDSA - not available from Sigma-Aldrich Canada; estupefaciente (Spain); Decreto Lei 15/93: Tabela IA (Portugal) application(s) HPLC: suitable, gas chromatography (GC): suitable solubility H2O: 62 mg/mL, ethanol: soluble Featured Industry Forensics and Toxicology
Veterinaryoriginator Abbott SMILES string O[C@H]([C@@H](O)C(O)=O)C(O)=O.[H][C@]12CCC(=O)[C@]3([H])Oc4c(OC)ccc5C[C@H]1N(C)CC[C@@]23c45 InChI 1S/C18H21NO3.C4H6O6/c1-19-8-7-18-11-4-5-13(20)17(18)22-16-14(21-2)6-3-10(15(16)18)9-12(11)19;5-1(3(7)8)2(6)4(9)10/h3,6,11-12,17H,4-5,7-9H2,1-2H3;1-2,5-6H,(H,7,8)(H,9,10)/t11-,12+,17-,18-;1-,2-/m01/s1 InChI key OJHZNMVJJKMFGX-BWCYBWMMSA-N
Safety InformationPersonal 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 Узнать цену -
Lidocaine N-ethyl bromide
Empirical Formula (Hill Notation): C16H27BrN2O CAS Number: 21306-56-9 Molecular Weight: 343.30 MDL number: MFCD00083182 PubChem Substance ID: 329817630 NACRES: NA.24
Кат. номер L5783-250MG-PW L5783-50MG-PW L5783-VAR L5783-50MG L5783-250MG ApplicationLidocaine N-ethyl bromide has been used as a standard in studying the demethylation effect of lidocaine N-ethyl bromide on breast cancer cells in vitro using colorimetric assay.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.Packaging50, 250 mg in poly bottleBiochem/physiol ActionsA quaternary derivative of lidocaine that is not membrane permeable. Blocks both fast Na+-dependent action potentials and voltage-dependent, non-inactivating Na+ conductance.Параметрыgrade analytical standard Quality Level 200 application(s) HPLC: suitable, gas chromatography (GC): suitable Featured Industry Forensics and Toxicology
Pharmaceutical (small molecule)
Veterinaryformat neat SMILES string [Br-].CC[N+](CC)(CC)CC(=O)Nc1c(C)cccc1C InChI 1S/C16H26N2O.BrH/c1-6-18(7-2,8-3)12-15(19)17-16-13(4)10-9-11-14(16)5;/h9-11H,6-8,12H2,1-5H3;1H InChI key DLHMKHREUTXMCH-UHFFFAOYSA-N
Safety InformationPersonal 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 Узнать цену -
Pantoprazole sodium hydrate
Empirical Formula (Hill Notation): C16H14F2N3O4S · Na · xH2O CAS Number: 718635-09-7 Molecular Weight: 405.35 (anhydrous basis) PubChem Substance ID: 329819976 NACRES: NA.77
Кат. номер P0021-50MG P0021-10MG ApplicationPantoprazole sodium hydrate has been used:- as a standard in high-performance liquid chromatography (HPLC){58
- as a prazole to study its effects on prodrug activation and human immunodeficiency virus 1 (HIV-1) inhibition
- to study its effects on breast cancer resistance protein (BCRP) inhibitors in various in vitro membrane preparations from various cell lines
Packaging10, 50 mg in glass bottleBiochem/physiol ActionsPantoprazole has the potential to treat symptoms of heartburn and acid regurgitation. It also has been studied to treat Helicobacter pylori infection and duodenal ulcer.
Pantoprazole is a benzimidazole derivative,activated in acidic environment. It is useful in treating long term prophylaxis and acid-related disorders.
Pantoprazole is a gastric proton pump inhibitor.Features and BenefitsThis compound was developed by Novartis. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.
This compound is featured on the Acid-Sensing (Proton-gated) Ion Channels (ASICs) page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.ПараметрыQuality Level 100 assay 98% (HPLC) form powder storage condition desiccated application(s) HPLC: suitable, gas chromatography (GC): suitable color white to off-white solubility H2O: 20 mg/mL originator Novartis storage temp. 20°C SMILES string O.[Na+].COc1ccnc(CS(=O)c2nc3cc(OC(F)F)ccc3[n-]2)c1OC InChI 1S/C16H14F2N3O4S.Na.H2O/c1-23-13-5-6-19-12(14(13)24-2)8-26(22)16-20-10-4-3-9(25-15(17)18)7-11(10)21-16;;/h3-7,15H,8H2,1-2H3;;1H2/q-1;+1; InChI key CGJRLPRCWSHOFU-UHFFFAOYSA-N Gene Information human ... ATP4A(495), ATP4B(496)
Safety Informationpictograms GHS07 signalword Warning hcodes H302 RIDADR NONH for all modes of transport WGK Germany WGK 1 Flash Point F Not applicable Flash Point C Not applicable Узнать цену -
Pilocarpine hydrochloride
Empirical Formula (Hill Notation): C11H16N2O2 · HCl CAS Number: 54-71-7 Molecular Weight: 244.72 Beilstein/REAXYS Number: 4034491 EC Number: 200-212-5 MDL number: MFCD00012722 PubChem Substance ID: 24277862 NACRES: NA.77
Кат. номер P6503-10G P6503-5G P6503-50G P6503-1G ApplicationPilocarpine hydrochloride has been used to stimulate salivary secretions in mice. It has also been used to induce status epilepticus(SE) in rat.Packaging5, 10, 50 g in poly bottleBiochem/physiol ActionsPilocarpine is alkaloid isolated from the shrub Pilocarpus species. It comprises imidazole ring and - lactone rings in its structure. It has cholinergic potential and it stimulates the parasympathetic system. Pilocarpine is also effective for treating glaucoma. It stimulates ciliary muscle contraction by binding to muscarinic M3 receptors. It is effective in treating corneal dryness in Sjogrens syndrome. It is a secretagogue, which improves salivary secretions in Xerostomia or a dry mouth condition in Sjogrens syndrome patients and in radiotherapy patients with head and neck carcinoma.
Nonselective muscarinic acetylcholine receptor agonist; used to produce an experimental model of epilepsy.Features and BenefitsThis compound is a featured product for ADME Tox and Neuroscience research. Discover more featured ADME Tox and Neuroscience products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.
This compound is featured on the Acetylcholine Receptors (Muscarinic) page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, 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.CautionHygroscopic, light sensitiveOther NotesShelf life of the powder is at least five years.Legal InformationLOPAC is a registered trademark of Sigma-Aldrich Co. LLCПараметрыQuality Level 100 assay 99% (titration) form powder application(s) HPLC: suitable, gas chromatography (GC): suitable color white mp 202-205 °C (lit.) solubility H2O: 100 mg/mL Featured Industry Forensics and Toxicology
Veterinaryrelevant disease(s) epilepsy SMILES string Cl.CC[C@H]1[C@H](COC1=O)Cc2cncn2C InChI 1S/C11H16N2O2.ClH/c1-3-10-8(6-15-11(10)14)4-9-5-12-7-13(9)2;/h5,7-8,10H,3-4,6H2,1-2H3;1H/t8-,10-;/m0./s1 InChI key RNAICSBVACLLGM-GNAZCLTHSA-N Gene Information human ... CHRM1(1128), CHRM2(1129), CHRM3(1131), CHRM4(1132), CHRM5(1133)
Safety Informationpictograms GHS06 signalword Danger hcodes H300 + H330 pcodes P301 + P310 + P330 - P304 + P340 + P310 RIDADR UN 1544PSN2 6.1 / PGII WGK Germany WGK 3 Узнать цену -
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
Кат. номер S8139-5G S8139-25G ApplicationTreatment 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.29Packaging5, 25 g in poly bottleBiochem/physiol ActionsSulindac 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 BenefitsThis 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.Legal InformationLOPAC is a registered trademark of Sigma-Aldrich Co. LLCПараметрыQuality 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
Veterinaryoriginator 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)
Safety Informationpictograms 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 Узнать цену
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