| Identification | More | [Name]
ISOOCTYL THIOGLYCOLATE | [CAS]
25103-09-7 | [Synonyms]
ACETIC ACID, MERCAPTO, ISOOCTYL ESTER
IOTG
IOTG(TM)
ISOOCTYL THIOGLYCOLATE
ISOOCTYLTHIOGLYCOLLATE
MERCAPTOACETIC ACID ISOOCTYL ESTER
THIOGLYCOLIC ACID ISOOCTYL ESTER
6-Methylheptyl sulfanylacetate
isooctylmercaptoacetate
iso-Octylmercaptoacetate
mercapto-aceticaciisooctylester
Thioglycolic Acod Isooctyl Ester
IsooctylThioglycoalte
Isooctylmercaptoacetat
THIOGLYCOLIC ACID ISOOCTYL ESTER: 90% (MIXED BRANCHED ISOMER)
ISOOCTYL THIOGLYCOLATE (ISOOCTYL MERCAPTOACETATE)
Isooctyl Thioglycolate (mixed branched isomer)
Thioglycollic acid 6-methylheptyl ester | [EINECS(EC#)]
246-613-9 | [Molecular Formula]
C10H20O2S | [MDL Number]
MFCD00022088 | [Molecular Weight]
204.33 | [MOL File]
25103-09-7.mol |
| Chemical Properties | Back Directory | [Appearance]
Water-white liquid; faint fruity odor. Combustible. | [Melting point ]
<-50°C | [Boiling point ]
96°C | [density ]
0,97 g/cm3 | [vapor pressure ]
3.1Pa at 20℃ | [refractive index ]
1.4590 to 1.4640 | [Fp ]
133°C | [storage temp. ]
Store below +30°C. | [form ]
liquid | [Water Solubility ]
10.6mg/L at 20℃ | [Cosmetics Ingredients Functions]
HAIR WAVING OR STRAIGHTENING | [Cosmetic Ingredient Review (CIR)]
ISOOCTYL THIOGLYCOLATE (25103-09-7) | [InChI]
InChI=1S/C10H20O2S/c1-9(2)6-4-3-5-7-12-10(11)8-13/h9,13H,3-8H2,1-2H3 | [InChIKey]
RZBBHEJLECUBJT-UHFFFAOYSA-N | [SMILES]
C(=O)(CS)OCCCCCC(C)C | [LogP]
3.68 at 20℃ | [Uses]
Antioxidants, fungicides, oil additives, plasticizers, insecticides, stabilizers, polymerization
modifiers, stabilizer in tin-sulfur compounds, stripping agent for polysulfide rubber. | [CAS DataBase Reference]
25103-09-7(CAS DataBase Reference) | [EPA Substance Registry System]
Acetic acid, mercapto-, isooctyl ester (25103-09-7) |
| Hazard Information | Back Directory | [Hazard]
Toxic by ingestion. | [Chemical Properties]
Water-white liquid; faint fruity odor. Combustible. | [Synthesis]
Chloroacetic acid and isooctyl alcohol are esterified in the presence of toluene solvent and sulfuric acid catalyst to produce isooctyl chloroacetate. After neutralization, sodium thiosulfate is added and reacted in ethanol solvent to produce sodium thiosulfate isooctyl chloroacetate. Then, acid hydrolysis is carried out with hydrochloric acid to produce Isooctyl thioglycolate. |
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