Detergents

Reported to be useful in solubilizing membrane proteins.
Tetraethylene glycol monooctyl ether has been used in a study to assess thermal diffusion behavior of nonionic surfactants in water. It has also been used in a study to investigate unusual micelle and surface adsorption behavior in mixtures of surfactants.

description	non-ionic
Quality Level	200,
assay	≥98% (GC)
form	liquid
mol wt	306.44 g/mol
density	0.969 g/mL at 20 °C (lit.)
SMILES string	CCCCCCCCOCCOCCOCCOCCO
InChI	1S/C16H34O5/c1-2-3-4-5-6-7-9-18-11-13-20-15-16-21-14-12-19-10-8-17/h17H,2-16H2,1H3
InChI key	FEOZZFHAVXYAMB-UHFFFAOYSA-N

Tetramethylammonium binds AT-rich DNA polymers while concomitantly abolishing the preferential melting of AT versus GC base pairs. Supplied as 0.2 μm filtered solution in 18 megohm water.

pictograms	GHS07
signalword	Warning
hcodes	H315 - H319 - H335
pcodes	P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	Eyeshields,, Gloves,, type ABEK (EN14387) respirator filter,
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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Tetraglycol

CAS Number: 31692-85-0

MDL number: MFCD00801146

NACRES: NA.25

Кат. номер

T3396-1KG

T3396-100G

T3396-250G

Application
Used as solvent to dissolve water-insoluble compounds.
Caution
Do not confuse with tetraethylene glycol, which is also sometimes called tetraglycol.
Параметры

description non-ionic

Quality Level 200,

product line BioXtra

density 1.09 g/mL at 25 °C (lit.)

InChI 1S/C7H14O3/c8-3-5-9-6-7-2-1-4-10-7/h7-8H,1-6H2

InChI key CTPDSKVQLSDPLC-UHFFFAOYSA-N

Safety Information

Personal Protective Equipment 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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Tetramethylammonium chloride solution

CAS Number:	75-57-0
MDL number:	MFCD00011628
PubChem Substance ID:	24900143
NACRES:	NA.31

Quality Level	200,
grade	for molecular biology
concentration	5 M
foreign activity	DNase, RNase, none detected
SMILES string	[Cl-].C[N+](C)(C)C
InChI	1S/C4H12N.ClH/c1-5(2,3)4;/h1-4H3;1H/q+1;/p-1
InChI key	OKIZCWYLBDKLSU-UHFFFAOYSA-M

Tetramethylammonium hydroxide pentahydrate is a clathrate hydrate which has been found to be a fast “proton” or “hydroxide ion” conductor.

pictograms	GHS06,GHS08,GHS09
signalword	Danger
hcodes	H301 + H311 - H315 - H370 - H411
pcodes	P273 - P280 - P301 + P310 + P330 - P302 + P352 + P312
Target Organs	Central nervous system
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type ABEK (EN14387) respirator filter,
RIDADR	UN 2810 6.1 / PGIII
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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Tetramethylammonium hydroxide pentahydrate

Empirical Formula (Hill Notation):	C₄H₁₃NO · 5H₂O
Linear Formula:	(CH₃)₄N(OH) · 5H₂O
CAS Number:	10424-65-4
Molecular Weight:	181.23
Beilstein/REAXYS Number:	3714235
EC Number:	200-882-9
MDL number:	MFCD00149566
PubChem Substance ID:	24900455
NACRES:	NA.25

Tetramethylammonium hydroxide pentahydrate has been used in a study to assess strains of Pseudomnas species by a single-step gas chromatographic characterization procedure. It has also been used in a study to investigate solid-state metal hydride batteries nickel oxyhydroxide-metal hydride and manganese dioxide-metal hydride.

1 kg in glass bottle
5, 25, 100 g in glass bottle

vapor density	1.1 (vs air)
Quality Level	200,
description	non-ionic
assay	≥97%
autoignition temp.	878 °F
mol wt	181.23 g/mol
expl. lim.	36 %
mp	67-70 °C (lit.)
SMILES string	O.O.O.O.O.[OH-].C[N+](C)(C)C
InChI	1S/C4H12N.6H2O/c1-5(2,3)4;;;;;;/h1-4H3;6*1H2/q+1;;;;;;/p-1
InChI key	MYXKPFMQWULLOH-UHFFFAOYSA-M

Thesit has been used in the reaction buffer to reduce the background sedimentation.
Suggested substitute for Lubrol in the preparation of G protein from bovine brain.

pictograms	GHS05,GHS06,GHS08,GHS09
signalword	Danger
hcodes	H300 + H310 - H314 - H370 - H372 - H411
pcodes	P260 - P273 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338
Target Organs	Central nervous system
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type P1 (EN143) respirator filter,, type P3 (EN 143) respirator cartridges,
RIDADR	UN 3423 8 / PGII
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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Thesit®

Linear Formula:	HO(CH₂CH₂O)_n(CH₂)₁₁CH₃
CAS Number:	9002-92-0
MDL number:	MFCD00080891
PubChem Substance ID:	57653299
NACRES:	NA.21

Thesit/Polidocanol possesses in vitro and in vivo anti-angiogenic effects. This sclerosant is mainly used for sclerotherapy.

Thesit is a registered trademark of Desitin Arzneimittel GmbH

grade	for membrane research
Quality Level	200,
description	non-ionic
mol wt	average mol wt 583
impurities	1 ppm peroxides (as H₂O₂)
CMC	0.1 mM (20-25°C)
SMILES string	CCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO
InChI	1S/C58H118O24/c1-2-3-4-5-6-7-8-9-10-11-13-60-15-17-62-19-21-64-23-25-66-27-29-68-31-33-70-35-37-72-39-41-74-43-45-76-47-49-78-51-53-80-55-57-82-58-56-81-54-52-79-50-48-77-46-44-75-42-40-73-38-36-71-34-32-69-30-28-67-26-24-65-22-20-63-18-16-61-14-12-59/h59H,2-58H2,1H3
InChI key	IEQAICDLOKRSRL-UHFFFAOYSA-N

Trehalose is commonly used as a stabilizer and protective material for biomaterial compounds. Because of these characteristics, Trehalose is introduced as a hydrophilic part. Due to these properties of Trehalose, protein degeneration is expected to be prevented with Trehalose detergents. Therefore, Trehalose detergents may keep the function of the protein and be utilized in the field of proteomics research.

pictograms	GHS05,GHS07,GHS09
signalword	Danger
hcodes	H302 - H315 - H318 - H410
pcodes	P264 - P273 - P280 - P301 + P312 - P302 + P352 - P305 + P351 + P338
Personal Protective Equipment	dust mask type N95 (US),, Eyeshields,, Gloves,
RIDADR	NONH for all modes of transport
WGK Germany	WGK 2
Flash Point F	235.4 °F - closed cup
Flash Point C	113 °C - closed cup

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Trehalose 6-decanoate

Empirical Formula (Hill Notation):	C₂₂H₄₀O₁₂
CAS Number:	924885-56-3
Molecular Weight:	496.55
PubChem Substance ID:	329753561
NACRES:	NA.25

Quality Level	100,
assay	≥95.0% (GC)
mol wt	496.55 g/mol
application(s)	protein quantification: suitable
CMC	3 mM
storage temp.	2-8°C
SMILES string	O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@H]2O[C@H](COC(CCCCCCCCC)=O)[C@@H](O)[C@H](O)[C@H]2O
InChI	1S/C22H40O12/c1-2-3-4-5-6-7-8-9-14(24)31-11-13-16(26)18(28)20(30)22(33-13)34-21-19(29)17(27)15(25)12(10-23)32-21/h12-13,15-23,25-30H,2-11H2,1H3/t12?,13?,15-,16-,17?,18?,19+,20+,21-,22-/m1/s1
InChI key	NWUMPUQFMKERLR-FLRCUGBKSA-N

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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Trehalose 6-dodecanoate

Empirical Formula (Hill Notation):	C₂₄H₄₄O₁₂
CAS Number:	64622-91-9
Molecular Weight:	524.60
PubChem Substance ID:	329753546
NACRES:	NA.25

Quality Level	100,
assay	≥95.0% (GC)
mol wt	524.60 g/mol
application(s)	protein quantification: suitable
CMC	0.15 mM
storage temp.	2-8°C
SMILES string	O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@H]2O[C@H](COC(CCCCCCCCCCC)=O)[C@@H](O)[C@H](O)[C@H]2O
InChI	1S/C24H44O12/c1-2-3-4-5-6-7-8-9-10-11-16(26)33-13-15-18(28)20(30)22(32)24(35-15)36-23-21(31)19(29)17(27)14(12-25)34-23/h14-15,17-25,27-32H,2-13H2,1H3/t14?,15?,17-,18-,19?,20?,21+,22+,23-,24-/m1/s1
InChI key	LISGDTVWONGLJR-VOEYTPSHSA-N

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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Trehalose 6-hexadecanoate

Empirical Formula (Hill Notation):	C₂₈H₅₂O₁₂
CAS Number:	42939-93-5
Molecular Weight:	580.71
PubChem Substance ID:	329753539
NACRES:	NA.25

Quality Level	100,
assay	≥95.0% (GC)
mol wt	580.71 g/mol
CMC	0.0061 mM
storage temp.	2-8°C
SMILES string	O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@H]2O[C@H](COC(CCCCCCCCCCCCCCC)=O)[C@@H](O)[C@H](O)[C@H]2O
InChI	1S/C28H52O12/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-20(30)37-17-19-22(32)24(34)26(36)28(39-19)40-27-25(35)23(33)21(31)18(16-29)38-27/h18-19,21-29,31-36H,2-17H2,1H3/t18?,19?,21-,22-,23?,24?,25+,26+,27-,28-/m1/s1
InChI key	VNHFMAKRYDWMAF-DHFWNHDGSA-N

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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Trehalose 6-octanoate

Empirical Formula (Hill Notation):	C₂₀H₃₆O₁₂
CAS Number:	64622-90-8
Molecular Weight:	468.49
PubChem Substance ID:	329760885
NACRES:	NA.25

Quality Level	100,
assay	≥95.0% (GC)
mol wt	468.49 g/mol
CMC	5.6 mM
storage temp.	2-8°C
SMILES string	O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@@H]1O[C@H]2O[C@H](COC(CCCCCCC)=O)[C@@H](O)[C@H](O)[C@H]2O
InChI	1S/C20H36O12/c1-2-3-4-5-6-7-12(22)29-9-11-14(24)16(26)18(28)20(31-11)32-19-17(27)15(25)13(23)10(8-21)30-19/h10-11,13-21,23-28H,2-9H2,1H3/t10?,11?,13-,14-,15?,16?,17+,18+,19-,20-/m1/s1
InChI key	WNPJPTWSRIRPIJ-LPKQXWMESA-N

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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Tridecyl -D-maltoside 16321-1G

Empirical Formula (Hill Notation):	C₂₅H₄₈O₁₁
CAS Number:	93911-12-7
Molecular Weight:	524.64
MDL number:	MFCD08062386
PubChem Substance ID:	329751187
NACRES:	NA.25

description	non-ionic
Quality Level	100,
assay	99.0% (TLC)
application(s)	electrophoresis: suitable, protein purification: suitable, protein quantification: suitable
solubility	H₂O: 10 mg/mL, clear, colorless
SMILES string	CCCCCCCCCCCCCO[C@@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O
InChI	1S/C25H48O11/c1-2-3-4-5-6-7-8-9-10-11-12-13-33-24-22(32)20(30)23(17(15-27)35-24)36-25-21(31)19(29)18(28)16(14-26)34-25/h16-32H,2-15H2,1H3/t16-,17-,18-,19+,20-,21-,22-,23-,24-,25-/m1/s1
InChI key	JZPRPDMVGIRGBV-IYBATYGCSA-N

Triethylene glycol monomethyl ether (TEGME) was used in the following studies:

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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Triethylene glycol monomethyl ether

Empirical Formula (Hill Notation):	C₇H₁₆O₄
Linear Formula:	CH₃(OCH₂CH₂)₃OH
CAS Number:	112-35-6
Molecular Weight:	164.20
Beilstein/REAXYS Number:	1700198
EC Number:	203-962-1
MDL number:	MFCD00002875
PubChem Substance ID:	329769908
NACRES:	NA.23

To study the structural and thermosensitive properties of phosphazene derivatives having glycol and amino acids groups.
Synthesis of amphiphilic o-phenylene ethylene oligomers.
Preparation of pegylated zinc(II) phthalocyanines.
Modification of 2-OH positions in cyclodextrin thioethers, which are used for transport of hydrophobic drugs.
Functionalizing polymethacrylic acid (PMMA), hence increasing inhibition in crack generation in TEGMA-PMMA compared to unmodified PMMA electrodes.
Preparation of difunctionalized ionic liquids (ILs).
As terminal groups for cationic dendrons, which was further used to encapsulate an inorganic polyanionic cluster.

Quality Level	200,
vapor density	5.66 (vs air)
vapor pressure	<0.01 mmHg ( 20 °C)
description	non-ionic
grade	purum
assay	97.0% (GC)
mol wt	164.20 g/mol
refractive index	n20/D 1.439 (lit.), n20/D 1.439
bp	122 °C/10 mmHg (lit.)
density	1.026 g/mL at 25 °C (lit.)
SMILES string	COCCOCCOCCO
InChI	1S/C7H16O4/c1-9-4-5-11-7-6-10-3-2-8/h8H,2-7H2,1H3
InChI key	JLGLQAWTXXGVEM-UHFFFAOYSA-N

Personal Protective Equipment	Eyeshields,, Gloves,
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point F	230.0 °F - closed cup
Flash Point C	110 °C - closed cup

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Trimethyloctadecylammonium chloride 53112-10G

Empirical Formula (Hill Notation):	C₂₁H₄₆ClN
Linear Formula:	CH₃(CH₂)₁₇N(Cl)(CH₃)₃
CAS Number:	112-03-8
Molecular Weight:	348.05
Beilstein/REAXYS Number:	3917847
EC Number:	203-929-1
MDL number:	MFCD00050188
PubChem Substance ID:	329757914
NACRES:	NA.25

Quality Level	100,
assay	95.0% (calc. on dry substance, T)
mol wt	348.05 g/mol
application(s)	electrophoresis: suitable, protein quantification: suitable
impurities	3.0% water
pH	5.5-8.5 (20 °C, 0.05% in H₂O)
	0.05 % in H₂O
UV absorption	: 225 nm A_max: 0.08, : 260 nm A_max: 0.06, : 280 nm A_max: 0.04, : 340 nm A_max: 0.02
SMILES string	[Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C
InChI	1S/C21H46N.ClH/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22(2,3)4;/h5-21H2,1-4H3;1H/q+1;/p-1
InChI key	VBIIFPGSPJYLRR-UHFFFAOYSA-M

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product is a biodegradable surfactant and is aligned with the 10th principle of Green Chemistry "Design for Degradation".
Triton CG-110 is a mixture of 58.0-62.0% D-glucopyranose, oligomeric, decyl octyl glycoside and 38.0-42.0% water. Contains less than 2% decanol and less than 1.0% octanol.

pictograms	GHS05,GHS07,GHS09
signalword	Danger
hcodes	H302 + H312 - H314 - H410
pcodes	P260 - P273 - P280 - P301 + P312 - P303 + P361 + P353 - P305 + P351 + P338
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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Triton™ CG-110

CAS Number:	68515-73-1
NACRES:	NA.21

Triton™ CG-110 can be used:

In the preparation of multilamellar vesicles as carriers for tretinoins and retinoids.
In the study of mineralization, leaching, and adsorption of glyphosate herbicide in the soil.

100, 500 mL in poly bottle

Features and Benefits

Mild
Good detergency & wetting properties
Lower color than Triton BG-10
Readily biodegradable
Moderate to high stable foam

Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

Quality Level	100,
grade	laboratory grade
description	non-ionic
form	liquid
greener alternative product characteristics	Design for Degradation Learn more about the Principles of Green Chemistry,.
CMC	1748 ppm (25°C)
transition temp	pour point -15 °C, cloud point >100 °C (1 wt% actives aq solution)
solubility	water: freely soluble at 20 °C (visual)
density	1.15 g/mL at 20 °C
greener alternative category	Aligned,

Triton™ N-57 is a surfactant with the ability to combat algal parasites Phlyctidium scenedesmi (Fott) and Phlyctidium sp.

pictograms	GHS05
signalword	Danger
hcodes	H315 - H318
pcodes	P264 - P280 - P302 + P352 - P305 + P351 + P338 - P332 + P313 - P362 + P364
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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Triton™ N-57

MDL number:	MFCD00132490
NACRES:	NA.25

Triton™ N-57 has been used in a study to assess calcium activated neutral proteinase activity in brain and other tissue of rat. It has also been used in a study to synthesize fine silica powders from sodium silicate at room temperature.

Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

description	non-ionic
Quality Level	100,
application(s)	permeability assay: suitable

Triton™ QS-15 anionic surfactant which can be used in buffer systems for micellar electrokinetic chromatography (MEKC).

pictograms	GHS07
signalword	Warning
hcodes	H319
pcodes	P305 + P351 + P338
Personal Protective Equipment	Eyeshields,, Gloves,, type ABEK (EN14387) respirator filter,
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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Triton™ N-60

MDL number: MFCD00132490

NACRES: NA.25

Кат. номер

N60-100ML

N60-500ML

N60-1GA

General description
Triton N-60 is a planar aromatic species with an approximate length of 10 .
Application
Triton N-60 has been used in a study to assess the use of surfactant solutions for dust suppression in coal mines. It has also been used in a study to describe a spectrophotometric assay for determination of critical micelle concentration of nonionic detergent solutions.
Packaging
100 mL in poly bottle
Legal Information
Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow
Параметры

description non-ionic

Quality Level 100,

Safety Information

RIDADR UN 3082 9 / PGIII

WGK Germany WGK 3

Flash Point F Not applicable

Flash Point C Not applicable

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Triton™ QS-15

CAS Number:	11105-10-5
MDL number:	MFCD01867807
NACRES:	NA.25

Triton™ QS-15 has been used in a study to assess the solubilization and purification of cholinephosphotransferase in hamster tissues. It has also been used in a study to investigate the inhibition of calmodulin-activated cyclic nucleotide phosphodiesterase.

100 mL in poly bottle

Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

description	anionic
Quality Level	200,
density	1.116 g/mL at 25 °C

Triton™ X-100 is a common non-ionic surfactant and emulsifier which is often used in biochemical applications to solubilize proteins. It is considered a comparatively mild detergent, non-denaturing, and is reported in numerous references as a routinely added reagent. It is utilized for lysing cells to extract protein and cellular organelles. It can also permeabilize the living cell membrane for transfection.
Triton X-100 has hemolytic property and is used for DNA extraction.

pictograms	GHS07
signalword	Warning
hcodes	H315 - H319 - H335
pcodes	P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	Eyeshields,, Gloves,, type ABEK (EN14387) respirator filter,
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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Triton™ X-100

Linear Formula:	t-Oct-C₆H₄-(OCH₂CH₂)_xOH, x= 9-10
CAS Number:	9036-19-5
Beilstein/REAXYS Number:	2315025
MDL number:	MFCD00128254
PubChem Substance ID:	329830772
NACRES:	NA.21

Triton™-X has been used:

In the permeabilization of cells for immunofluorescence staining
As a component of lysis buffer in western blot analysis
As a component of Tris-buffered saline for the preparation of cell sections in Immunogold labelling for electron microscope

5 mL in glass bottle
1 gal in poly bottle
5 gal in poly drum
1 L in poly bottle
100, 500 mL in poly bottle

Widely used non-ionic surfactant for recovery of membrane components under mild non-denaturing conditions.

Tri-Chek is a trademark of Micro Essential Laboratory, Inc.
Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

Quality Level	200
grade	laboratory grade
description	non-ionic
form	liquid
mol wt	micellar avg mol wt 80,000, average mol wt 625
aggregation number	100-155
CMC	0.2-0.9 mM (20-25°C)
transition temp	cloud point 65 °C, pour point ~7 °C
solubility	water: 0.1 mL/mL, clear to slightly hazy, colorless to faintly yellow
HLB	13.5
SMILES string	CC(C)(C)CC(C)(C)c1ccc(OCCOCCOCCOCCOCCOCCOCCO)cc1
InChI	1S/C28H50O8/c1-27(2,3)24-28(4,5)25-6-8-26(9-7-25)36-23-22-35-21-20-34-19-18-33-17-16-32-15-14-31-13-12-30-11-10-29/h6-9,29H,10-24H2,1-5H3
InChI key	HNLXNOZHXNSSPN-UHFFFAOYSA-N

Triton X-100 reduced, is a nonionic surfactant which has a hydrophilic polyethylene oxide chain.

Pictograms	GHS05,GHS07,GHS09
Signal Word	Danger
Hazard Statements	H302 - H315 - H318 - H410
Precautionary Statements	P273 - P280 - P301 + P312 + P330 - P302 + P352 - P305 + P351 + P338 + P310
Personal Protective Equipment	Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter, type N95 (US)
RIDADR	UN 3082 9 / PGIII
WGK Germany	WGK 2
Flash Point(F)	483.8 °F
Flash Point(C)	251 °C

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Triton™ X-100 reduced

Linear Formula:	4-(C₈H₁₇)C₆H₁₀(OCH₂CH₂)_nOH, n~10
CAS Number:	92046-34-9
MDL number:	MFCD00132505
NACRES:	NA.25

Triton X-100 reduced, a nonionic surfactant which has a hydrophilic polyethylene oxide chain, is a common laboratory detergent used for applications such as cell lysis and membrane permeabilization as a component of lysis buffers. Triton X-100 is used for the isolation of lipid rafts.

Hydrogenated to reduce UV absorbance.

5, 25 g in glass bottle

Preparation Note

Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

description	non-ionic
Quality Level	100,
mol wt	micellar average mol wt 80,000, average mol wt 625
aggregation number	100-155
refractive index	n20/D 1.473 (lit.)
CMC	0.2-0.9
transition temp	cloud point 65 °C
density	1.029 g/mL at 25 °C (lit.)
absorption	0.25 at 277 nm in H₂O at 0.5%
HLB	13.5

pictograms	GHS07,GHS09
signalword	Warning
hcodes	H315 - H319 - H335 - H411
pcodes	P273 - P302 + P352 - P305 + P351 + P338
Target Organs	Respiratory system
Personal Protective Equipment	dust mask type N95 (US),, Eyeshields,, Gloves,
RIDADR	UN 3082 9 / PGIII
WGK Germany	WGK 3
Flash Point F	235.4 °F - closed cup
Flash Point C	113 °C - closed cup

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Triton™ X-100 solution

Linear Formula:	t-Oct-C₆H₄-(OCH₂CH₂)_xOH, x= 9-10
CAS Number:	9036-19-5
Beilstein/REAXYS Number:	2315025
MDL number:	MFCD00128254
PubChem Substance ID:	57653560

Triton-X has been used:

for permeabilization of cells before techniques like indirect immunofluorescence and flow cytometry
As a component of lysis buffer used for homogenization of cells
As a component of blocking buffer in immunofluorescence staining
For the preparation of cells in double fluorescence staining

Widely used non-ionic surfactant for recovery of membrane components under mild non-denaturing conditions.

Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

Quality Level	200,
grade	for molecular biology
description	non-ionic
product line	BioUltra
mol wt	micellar avg mol wt 80,000, average mol wt 625
concentration	~10% in H₂O
aggregation number	100-155
impurities	DNases, none detected, RNases, none detected, insoluble matter, passes filter test, phosphatases, none detected, proteases, none detected
refractive index	n20/D 1.349±0.002
pH	6.5-8.5 (25 °C)
CMC	0.2-0.9 mM (20-25°C), 0.23 mM
transition temp	cloud point 65 °C, pour point ~7 °C
density	1.01 g/mL at 20 °C
cation traces	Al: 1 mg/kg, Ba: 1 mg/kg, Bi: 1 mg/kg, Ca: 5 mg/kg, Cd: 1 mg/kg, Co: 1 mg/kg, Cr: 1 mg/kg, Cu: 1 mg/kg, Fe: 1 mg/kg, K: 100 mg/kg, Li: 1 mg/kg, Mg: 1 mg/kg, Mn: 1 mg/kg, Mo: 1 mg/kg, Na: 100 mg/kg, Ni: 1 mg/kg, Pb: 1 mg/kg, Sr: 1 mg/kg, Zn: 1 mg/kg
absorption	cut-off at 310 nm
HLB	13.5
SMILES string	CC(C)(C)CC(C)(C)c1ccc(OCCOCCOCCOCCOCCOCCOCCO)cc1
InChI	1S/C28H50O8/c1-27(2,3)24-28(4,5)25-6-8-26(9-7-25)36-23-22-35-21-20-34-19-18-33-17-16-32-15-14-31-13-12-30-11-10-29/h6-9,29H,10-24H2,1-5H3
InChI key	HNLXNOZHXNSSPN-UHFFFAOYSA-N

pictograms	GHS05,GHS09
signalword	Danger
hcodes	H315 - H318 - H410
pcodes	P273 - P280 - P302 + P352 - P305 + P351 + P338 + P310
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type ABEK (EN14387) respirator filter,
RIDADR	NONH for all modes of transport
WGK Germany	WGK 2
Flash Point F	483.8 °F - closed cup
Flash Point C	251 °C - closed cup

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Triton™ X-102

CAS Number:	9036-19-5
MDL number:	MFCD00132490
NACRES:	NA.21

Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

description	non-ionic
Quality Level	200,
mol wt	757 g/mol
CMC	0.33 mM
transition temp	cloud point 88 °C
HLB	14.4
InChI	1S/C18H30O3/c1-17(2,3)14-18(4,5)15-6-8-16(9-7-15)21-13-12-20-11-10-19/h6-9,19H,10-14H2,1-5H3
InChI key	LBCZOTMMGHGTPH-UHFFFAOYSA-N

Triton™ X-114 is a nonionic detergent. It is a good detergent for solubilizing membranes having reversible phase-separation property useful for the separation of intrinsic membrane proteins. Solution of Triton™ X-114 is homogeneous at 0°C but phase separation into aqueous phase and a detergent phase occurs above 20°C. Phase separation of proteins in solutions of Triton™ X-114 has been investigated. This octylphenol ethoxylate is compatible with anionic, cationic, and other nonionic surfactants and chemically stable in most acidic & alkaline solutions.

pictograms	GHS05,GHS07,GHS09
signalword	Danger
hcodes	H302 - H315 - H318 - H410
pcodes	P280 - P301 + P312 + P330 - P305 + P351 + P338 + P310
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type ABEK (EN14387) respirator filter,
RIDADR	UN 3082 9 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Triton™ X-114

Linear Formula:	(C₂H₄O)n C₁₄H₂₂O, n = 7 or 8
CAS Number:	9036-19-5
Beilstein/REAXYS Number:	2315025
MDL number:	MFCD00128254
PubChem Substance ID:	24902129
NACRES:	NA.21

Triton™ X-114 has been used:

To remove endotoxin from solutions of protein using phase separation technique
In the extraction and purification of DNA from endotoxin
In the biphasic extraction of lipoproteins from bacterial cell wall
As a non-ionic detergent with a low cloud point (23 °C) enabling protein solubilization with phase-partitioning of hydrophilic from amphiphilic proteins

1 gal in poly bottle
5 gal in poly drum
1 L in poly bottle
100, 500 mL in poly bottle

Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

grade	laboratory grade
Quality Level	200,
description	non-ionic
mol wt	average mol wt 537
composition	t-Oct-C₆H₄-(OCH₂CH₂)_xOH, x = 7-8
refractive index	n20/D 1.488 (lit.)
CMC	0.2 mM (20-25°C)
transition temp	pour point ~9 °C, cloud point 23 °C
density	1.058 g/mL at 25 °C (lit.)
HLB	12.4
SMILES string	CC(C)(C)CC(C)(C)c1ccc(OCCOCCOCCOCCOCCOCCOCCO)cc1
InChI	1S/C28H50O8/c1-27(2,3)24-28(4,5)25-6-8-26(9-7-25)36-23-22-35-21-20-34-19-18-33-17-16-32-15-14-31-13-12-30-11-10-29/h6-9,29H,10-24H2,1-5H3
InChI key	HNLXNOZHXNSSPN-UHFFFAOYSA-N

pictograms	GHS05,GHS07,GHS09
signalword	Danger
hcodes	H302 - H315 - H318 - H410
pcodes	P264 - P273 - P280 - P301 + P312 - P302 + P352 - P305 + P351 + P338
Personal Protective Equipment	Eyeshields,, Gloves,, type ABEK (EN14387) respirator filter,
RIDADR	UN 3082 9 / PGIII
WGK Germany	WGK 3
Flash Point F	483.8 °F
Flash Point C	251 °C

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Triton™ X-165 solution

CAS Number:	9036-19-5
MDL number:	MFCD00132490
NACRES:	NA.21

Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

description	non-ionic
Quality Level	100,
mol wt	911 g/mol
application(s)	electrophoresis: suitable, protein quantification: suitable
CMC	0.43 mM
transition temp	cloud point >100 °C
HLB	15.5
InChI	1S/C18H30O3/c1-17(2,3)14-18(4,5)15-6-8-16(9-7-15)21-13-12-20-11-10-19/h6-9,19H,10-14H2,1-5H3
InChI key	LBCZOTMMGHGTPH-UHFFFAOYSA-N

Triton™ X-305 is a non-ionic surfactant. This octylphenol ethoxylate has higher number of ethylene oxide units, increased cmc (Critical micelle concentration) and hydrophile/lipophile balance when compared to Triton™ X-100. Triton X-305 is compatible with anionic, cationic, and other nonionic surfactants and chemically stable in most acidic and alkaline solutions.

pictograms	GHS05,GHS09
signalword	Danger
hcodes	H315 - H318 - H410
pcodes	P264 - P273 - P280 - P302 + P352 - P305 + P351 + P338 - P332 + P313
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type ABEK (EN14387) respirator filter,
RIDADR	UN 3082 9 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Triton™ X-305 solution

CAS Number:	9002-93-1
MDL number:	MFCD00132490
NACRES:	NA.21

Triton™ X-305 has been used:

In the treatment of cells for immunocytochemistry
Along with peroxotungstic acid in the preparation of tungsten trioxide films by sol-gel method
In the dispersion polymerization of styrene with activated poly(N-vinylpyrrolidone) (PVP) for the synthesis of lanthanide-encoded polystyrene particles

Tri-Chek is a trademark of Micro Essential Laboratory, Inc.
Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

description	non-ionic
Quality Level	200,
mol wt	~1526.0 g/mol
concentration	70% in H₂O
application(s)	blocking: suitable, cell culture \| mammalian: suitable, hybridization: suitable, immunohistochemistry: suitable, protein purification: suitable
CMC	0.65 mM
transition temp	cloud point >100 °C
HLB	17.3
InChI	1S/C16H26O2/c1-15(2,3)12-16(4,5)13-6-8-14(9-7-13)18-11-10-17/h6-9,17H,10-12H2,1-5H3
InChI key	JYCQQPHGFMYQCF-UHFFFAOYSA-N

1 L in poly bottle
100, 500 mL in poly bottle
1, 5 gal in poly bottle

pictograms	GHS05,GHS07,GHS09
signalword	Danger
hcodes	H302 - H315 - H318 - H410
pcodes	P273 - P280 - P301 + P312 + P330 - P302 + P352 - P305 + P351 + P338 + P310
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type ABEK (EN14387) respirator filter,
RIDADR	UN 3082 9 / PGIII
WGK Germany	WGK 2
Flash Point F	483.8 °F - closed cup
Flash Point C	251 °C - closed cup

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Triton™ X-405 solution

CAS Number:	9036-19-5
MDL number:	MFCD00128254
PubChem Substance ID:	329830805
NACRES:	NA.21

Caution

May precipitate on storage; redissolve at 50 °C

Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

description	non-ionic
Quality Level	100,
mol wt	~1967.0 g/mol
concentration	70% in H₂O
application(s)	ELISA: suitable
CMC	0.81 mM
transition temp	cloud point >100 °C
density	1.096 g/mL at 25 °C
HLB	17.6
SMILES string	CC(C)(C)CC(C)(C)c1ccc(OCCOCCOCCOCCOCCOCCOCCO)cc1
InChI	1S/C28H50O8/c1-27(2,3)24-28(4,5)25-6-8-26(9-7-25)36-23-22-35-21-20-34-19-18-33-17-16-32-15-14-31-13-12-30-11-10-29/h6-9,29H,10-24H2,1-5H3
InChI key	HNLXNOZHXNSSPN-UHFFFAOYSA-N

Triton™ X-45 is a non-ionic surfactant that has a low hydrophile–lypophile balance (HLB) value. It easily disperses in aqueous solution at room temperature. It is useful in bioseparation processes. Triton X-45 is compatible with anionic, cationic, and other nonionic surfactants and chemically stable in most acidic and alkaline solutions.

pictograms	GHS05,GHS07,GHS09
signalword	Danger
hcodes	H302 - H315 - H318 - H410
pcodes	P264 - P273 - P280 - P301 + P312 - P302 + P352 - P305 + P351 + P338
RIDADR	UN 3082 9 / PGIII
WGK Germany	WGK 3
Flash Point F	Not applicable
Flash Point C	Not applicable

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Triton™ X-45

Linear Formula:	t-Oct-C₆H₄-(OCH₂CH₂)_xOH, x= ~5
CAS Number:	9002-93-1
Beilstein/REAXYS Number:	2315025
MDL number:	MFCD00128254
PubChem Substance ID:	24902148
NACRES:	NA.21

Triton™ X-45 has been used along with tri-n-butyl phosphate (TnBP) in the treatment of human plasma for efficient inactivation of Hepatitis C virus before transfusion.

100 mL in poly bottle
1 L in poly bottle

Triton is a trademark of The Dow Chemical Company or an affiliated company of Dow

description	non-ionic
Quality Level	200,
application(s)	protein purification: suitable
transition temp	pour point ~26 °C
SMILES string	CC(C)(C)CC(C)(C)c1ccc(OCCOCCOCCOCCOCCOCCOCCO)cc1
InChI	1S/C28H50O8/c1-27(2,3)24-28(4,5)25-6-8-26(9-7-25)36-23-22-35-21-20-34-19-18-33-17-16-32-15-14-31-13-12-30-11-10-29/h6-9,29H,10-24H2,1-5H3
InChI key	HNLXNOZHXNSSPN-UHFFFAOYSA-N

During long periods of cold weather, and during storage at low temperatures, cloudiness or crystallization can occur in individual cases. These can be eliminated by stirring and gentle heating up to 40°C without any loss of quality.

pictograms	GHS05,GHS07,GHS09
signalword	Danger
hcodes	H302 - H315 - H318 - H410
pcodes	P273 - P280 - P301 + P312 + P330 - P302 + P352 - P305 + P351 + P338 + P310
Personal Protective Equipment	Eyeshields,, Faceshields,, Gloves,, type ABEK (EN14387) respirator filter,
RIDADR	UN 3082 9 / PGIII
WGK Germany	WGK 2
Flash Point F	483.8 °F
Flash Point C	251 °C

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Turkey red oil sodium salt

CAS Number:	68187-76-8
EC Number:	269-123-7
MDL number:	MFCD00132540

Quality Level	100,
grade	for microscopy
description	anionic
assay	100%
impurities	16-20% water (Karl Fischer)
pH	7-8 (10%)

Tween®20 is a polyoxyethylene sorbitol ester that belongs to the polysorbate family. It is a nonionic detergent having a molecular weight of 1,225 daltons, assuming 20 ethylene oxide units, 1 sorbitol, and 1 lauric acid as the primary fatty acid. The ethylene oxide subunits are responsible for the hydrophilic nature of the surfactant, while the hydrocarbon chains provide the hydrophobic environment. Sorbitol forms the backbone ring to which the ethylene oxide polymers are attached.

pictograms	GHS07
signalword	Warning
hcodes	H315 - H319
pcodes	P302 + P352 - P305 + P351 + P338
Personal Protective Equipment	Eyeshields,, Gloves,, type ABEK (EN14387) respirator filter,
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point F	228.2 °F - closed cup
Flash Point C	109 °C - closed cup

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TWEEN® 20

CAS Number:	9005-64-5
MDL number:	MFCD00165986
NACRES:	NA.21

TWEEN 20 is a nonionic detergent widely used in biochemical applications. It has been used as an emulsifying agent for the preparation of stable oil-in-water emulsions. TWEEN 20 has been used in pre-extraction of membranes to remove peripheral proteins (used at 2% for extraction of membrane-bound proteins).
TWEEN 20 has been used as a blocking agent for membrane based immunoassays at a typical concentration of 0.05%. TWEEN 20 can be used for lysing mammalian cells at a concentration of 0.005 to 0.5%.
TWEEN 20 has been used as a component of:

washing buffer and blocking buffer in Western blotting
blocking buffer in immunohistochemistry
washing buffer in ELISA (enzyme linked immunosorbent assay)
reaction mixture in PCR (polymerase chain reaction)

Non-ionic detergent

1, 4 L in poly bottle
25, 100, 250, 500, 6×500 mL in poly bottle
P1379-1KT:
Each kit contains 3 x 100ML samples, each sample from a uniquely manufactured lot.

Preparation Note

TWEEN 20 is miscible in water (100mg/mL), yielding a clear, yellow solution. It is also miscible with alcohol, dioxane, and ethyl acetate. TWEEN 20 is insoluble in liquid paraffin and fixed oils.

TWEEN is a registered trademark of Croda International PLC

Quality Level	300
description	non-ionic
assay	40.0% (GC)
form	viscous liquid
mol wt	~1228
composition	lauric acid, 40% (balance primarily myristic, palmitic, and stearic acids)
application(s)	DNA extraction: suitable, RNA extraction: suitable, cell culture \| mammalian: suitable, protein purification: suitable
impurities	3.0% water
refractive index	n20/D 1.468 (lit.)
CMC	0.06 mM (20-25°C)
acid number	2.2 mg/g
hydroxyl value	96108 mg/g
transition temp	cloud point 76 °C
density	1.095 g/mL at 25 °C (lit.)
HLB	16.7
suitability	complies for IR spectroscopy
InChI	1S/C26H50O10/c1-2-3-4-5-6-7-8-9-10-11-24(30)34-19-18-31-20-22(32-15-12-27)26-25(35-17-14-29)23(21-36-26)33-16-13-28/h22-23,25-29H,2-21H2,1H3
InChI key	HMFKFHLTUCJZJO-UHFFFAOYSA-N

Polyoxyethylenesorbitan monopalmitate, or TWEEN 40, is a non-ionic detergent.

Personal Protective Equipment	Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point(F)	527.0 °F - Pensky-Martens closed cup
Flash Point(C)	275 °C - Pensky-Martens closed cup

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TWEEN® 40

CAS Number:	9005-66-7
MDL number:	MFCD00165345
NACRES:	NA.25

Non-ionic detergent used for cell lysis, nuclei isolation and cell fractionation.
Polyoxyethylenesorbitan monopalmitate, or TWEEN 40, has been used in a study to assess the determination of iodide in urine based on a chemiluminescence system. It has also been used in a study to investigate the delivery of astaxanthin and canthaxanthin to HepG2 cells.

100, 500 mL in poly bottle
1 gal in poly bottle

TWEEN is a registered trademark of Croda International PLC

description	non-ionic
Quality Level	100,
assay	~90.0% (GC)
form	viscous liquid
mol wt	estimated mol wt 1277
composition	Palmitic acid, ~90% (balance primarily stearic acid)
application(s)	DNA extraction: suitable, RNA extraction: suitable, cell culture \| mammalian: suitable, protein purification: suitable
CMC	0.027 (20-25°C)
HLB	15.6
InChI	1S/C26H50O10/c1-2-3-4-5-6-7-8-9-10-11-24(30)34-19-18-31-20-22(32-15-12-27)26-25(35-17-14-29)23(21-36-26)33-16-13-28/h22-23,25-29H,2-21H2,1H3
InChI key	HMFKFHLTUCJZJO-UHFFFAOYSA-N

Personal Protective Equipment	Eyeshields,, Gloves,
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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TWEEN® 60

CAS Number:	9005-67-8
MDL number:	MFCD01780110
NACRES:	NA.25

TWEEN 60 is a niosome.

Polyethylene glycol sorbitan monostearate, or TWEEN 60, has been used in a study to assess encapsulation of functional lipophilic components in surfactant-based colloidal delivery systems. It has also been used in a study to investigate doxorubicin loaded magneto-niosomes for targeted drug delivery.

100, 500 mL in poly bottle
1 gal in poly bottle

TWEEN is a registered trademark of Croda International PLC

Quality Level	100,
mol wt	estimated mol wt 1309
composition	stearic acid, 40-60% , total stearic and palmitic acid, 90%
application(s)	DNA extraction: suitable, RNA extraction: suitable, cell culture \| mammalian: suitable, protein purification: suitable
CMC	27 mg/L
density	1.044 g/mL at 25 °C (lit.)
HLB	14.9
InChI	1S/C26H50O10/c1-2-3-4-5-6-7-8-9-10-11-24(30)34-19-18-31-20-22(32-15-12-27)26-25(35-17-14-29)23(21-36-26)33-16-13-28/h22-23,25-29H,2-21H2,1H3
InChI key	HMFKFHLTUCJZJO-UHFFFAOYSA-N

TWEEN 65 is a fatty acid polyoxyethylene ester of sorbitan.

Personal Protective Equipment	Eyeshields,, Gloves,
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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TWEEN® 65

CAS Number:	9005-71-4
MDL number:	MFCD00165348
NACRES:	NA.25

TWEEN 65 has been used in a study as a carbon source for the reductive dechlorination of hexachlorobenzene in a mixed, methanogenic culture. It has also been used in a study to investigate its ability to stimulate growth of the hypocotyl of Amaranthus caudatus L.

250 g in poly bottle
1 kg in poly bottle

TWEEN is a registered trademark of Croda International PLC

description	non-ionic
Quality Level	300,
assay	35% palmitic acid basis (GC)
composition	Stearic acid, 40% (balance primarily palmitic acid)
application(s)	DNA extraction: suitable, RNA extraction: suitable, cell culture \| mammalian: suitable, protein purification: suitable

TWEEN® 80 has been used in drug vehicle solution for specific injections in mice and rats. It has been used for the determination of esterase activity in bacterial cells.
Non-ionic detergent used for selective protein extraction and isolation of nuclei from mammalian cell lines.

Personal Protective Equipment	Eyeshields,, Gloves,
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point F	300.2 °F - closed cup
Flash Point C	149.00 °C - closed cup

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TWEEN® 80

CAS Number:	9005-65-6
MDL number:	MFCD00082107
NACRES:	NA.21

1 L in poly bottle
25, 500 mL in poly bottle
1 gal in poly bottle

TWEEN® 80 is a polysorbate surfactant which helps in stabilizing proteins and in protein membrane studies. It is regularly used for the extraction of membrane proteins and isolation of nuclei from cells.

TWEEN is a registered trademark of Croda International PLC

Quality Level	200
description	non-ionic
form	viscous liquid
mol wt	micellar avg mol wt 79,000, average mol wt 1310
composition	Oleic acid, 58.0% (balance primarily linoleic, palmitic, and stearic acids)
aggregation number	60
application(s)	cell analysis: suitable
CMC	0.012 mM (20-25°C)
transition temp	cloud point 65 °C
density	1.064 g/cm³
HLB	15
InChI	1S/C32H60O10/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-30(36)40-25-24-37-27-29(39-22-19-34)32-28(38-21-18-33)26-31(42-32)41-23-20-35/h9-10,28-29,31-35H,2-8,11-27H2,1H3/b10-9+
InChI key	RGPBUVUVZKQNHD-MDZDMXLPSA-N

Personal Protective Equipment	Eyeshields, Gloves
RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point(F)	235.4 °F - closed cup
Flash Point(C)	> 113 °C - closed cup

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TWEEN® 80 solution

CAS Number:	9005-65-6
MDL number:	MFCD00082107
NACRES:	NA.21

10 mL in glass bottle

Non-ionic detergent used for selective protein extraction and isolation of nuclei from mammalian cell lines

Components

Contains BHT as an antioxidant.

Quality

Low Peroxide

TWEEN is a registered trademark of Croda International PLC

Quality Level	200,
description	non-ionic
concentration	10%
storage temp.	2-8°C
InChI	1S/C32H60O10/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-30(36)40-25-24-37-27-29(39-22-19-34)32-28(38-21-18-33)26-31(42-32)41-23-20-35/h9-10,28-29,31-35H,2-8,11-27H2,1H3/b10-9+
InChI key	RGPBUVUVZKQNHD-MDZDMXLPSA-N

A nonionic liquid polymer of the alkyl aryl polyether alcohol type. Used as a surfactant.

RIDADR	NONH for all modes of transport
WGK Germany	WGK 1
Flash Point F	Not applicable
Flash Point C	Not applicable

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TWEEN® 85

CAS Number: 9005-70-3

MDL number: MFCD01779641

NACRES: NA.25

Кат. номер

P4634-100ML

P4634-500ML

P4634-1GA

General description
Tween 85 is a polyoxyethylene sorbitan trioleate non-ionic surfactant.
Application
Tween 85 has been used in a study to assess the potential application of niosomes for the delivery of ammonium glycyrrhizinate for the treatment of inflammatory diseases. It has also been used in a study to investigate the joint-action of antifouling substances in copper-free paints.
Packaging
100, 500 mL in poly bottle
1 gal in poly bottle
Legal Information
TWEEN is a registered trademark of Croda International PLC
Параметры

description non-ionic

Quality Level 200,

assay 50% (GC)

composition Oleic acid, 50% (balance primarily C₁₀-C₁₈ fatty acids)

Safety Information

Personal Protective Equipment Eyeshields,, Gloves,

RIDADR NONH for all modes of transport

WGK Germany WGK 1

Flash Point F Not applicable

Flash Point C Not applicable

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Tyloxapol

CAS Number:	25301-02-4
MDL number:	MFCD00149002
PubChem Substance ID:	24900557
NACRES:	NA.25

Tyloxapol is a nonionic liquid polymer of the alkyl aryl polyether alcohol type. It is used as a surfactant to aid liquefaction. Tyloxapol is used in the development of non-ionic surfactant-based liposomes (niosomes) for use in drug delivery systems. Tyloxapol may be used to study its mechanism of protecting macrophages from endotoxins. Tyloxapol may be used to study is potential cell toxicitiy.

50 g in glass bottle

Quality Level	300,
CMC	0.018 mM
transition temp	cloud point 94.3 °C
SMILES string	[H]C([H])=O.OCCO.CC(C)(C)CC(C)(C)c1ccc(O)cc1
InChI	1S/C14H22O.C2H6O2.CH2O/c1-13(2,3)10-14(4,5)11-6-8-12(15)9-7-11;3-1-2-4;1-2/h6-9,15H,10H2,1-5H3;3-4H,1-2H2;1H2
InChI key	GWJOFBXSBDVUMH-UHFFFAOYSA-N

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	Eyeshields,, Gloves,, type ABEK (EN14387) respirator filter,
RIDADR	NONH for all modes of transport
WGK Germany	WGK 2
Flash Point F	235.4 °F - closed cup
Flash Point C	113 °C - closed cup

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Undecyl -D-maltoside 14578-500MG

Empirical Formula (Hill Notation):	C₂₃H₄₄O₁₁
CAS Number:	168037-13-6
Molecular Weight:	496.59
MDL number:	MFCD09750649
PubChem Substance ID:	329750536
NACRES:	NA.25

description	non-ionic
Quality Level	100,
assay	90% (GC)
mol wt	496.59 g/mol
impurities	0.01% undecanol, 5% -isomer
pH	7.5-8.5 (1% in H₂O)
solubility	H₂O: 20%, clear to very faintly turbid, colorless
	1 % in H₂O
UV absorption	: 225 nm A_max: 0.25, : 260 nm A_max: 0.15, : 280 nm A_max: 0.10, : 340 nm A_max: 0.05
suitability	corresponds to standard for fluorescence
SMILES string	CCCCCCCCCCCO[C@H]1O[C@H](CO)[C@@H](O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O
InChI	1S/C23H44O11/c1-2-3-4-5-6-7-8-9-10-11-31-22-20(30)18(28)21(15(13-25)33-22)34-23-19(29)17(27)16(26)14(12-24)32-23/h14-30H,2-13H2,1H3/t14-,15-,16-,17+,18-,19-,20-,21-,22+,23-/m1/s1
InChI key	UYEMNFYVTFDKRG-BFNKVOCASA-N

Ursodeoxycholic acid (UDCS) is a cell protectant used extensively to mitigate hepatic and biliary diseases. Ursodeoxycholic acid may be used to study its specific activities that range from reduction of cholesterol absorpition, cholesterol gallstone dissolution to suppression of immune response.

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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Ursodeoxycholic acid

Empirical Formula (Hill Notation):	C₂₄H₄₀O₄
CAS Number:	128-13-2
Molecular Weight:	392.57
Beilstein/REAXYS Number:	3219888
EC Number:	204-879-3
MDL number:	MFCD00003680
PubChem Substance ID:	24900651
NACRES:	NA.25

1, 5, 25 g in poly bottle

Other Notes

Tandem Mass Spectrometry data independently generated by Scripps Center for Metabolomics is available to view or download in PDF. U5127.pdf , Tested metabolites are featured on Scripps Center for Metabolomics METLIN Metabolite Database. To learn more, visit sigma.com/metlin.,

description	anionic detergent
Quality Level	200,
assay	≥99%
mol wt	392.57 g/mol
mp	203-204 °C (lit.)
SMILES string	C[C@H](CCC(O)=O)[C@H]1CC[C@H]2[C@@H]3[C@@H](O)C[C@@H]4C[C@H](O)CC[C@]4(C)[C@H]3CC[C@]12C
InChI	1S/C24H40O4/c1-14(4-7-21(27)28)17-5-6-18-22-19(9-11-24(17,18)3)23(2)10-8-16(25)12-15(23)13-20(22)26/h14-20,22,25-26H,4-13H2,1-3H3,(H,27,28)/t14-,15+,16-,17-,18+,19+,20+,22+,23+,24-/m1/s1
InChI key	RUDATBOHQWOJDD-UZVSRGJWSA-N
Gene Information	human ... NR1H4(9971)