Methyl thioglycolate
Methyl thioglycolate
  • CAS No.:2365-48-2
Other grades of this product :
Methyl thioglycolate Basic information
Product Name:Methyl thioglycolate
Synonyms:MERCAPTOACETIC ACID METHYL ESTER;METG;METHYL THIOGLYCOLATE;METHYL THIOGLYCOLLATE;METHYL MERCAPTOACETATE;THIOGLYCOLIC ACID METHYL ESTER;mercapto-aceticacimethylester;Methanethiol, methoxy-
CAS:2365-48-2
MF:C3H6O2S
MW:106.14
EINECS:219-121-7
Product Categories:2365-48-2
Mol File:2365-48-2.mol
Methyl thioglycolate Chemical Properties
Melting point -24 °C
Boiling point 42-43 °C/10 mmHg (lit.)
density 1.187 g/mL at 25 °C (lit.)
refractive index n20/D 1.466(lit.)
Fp 86 °F
storage temp. Store below +30°C.
solubility 40g/l
form Liquid
pka8.04±0.10(Predicted)
color Clear colorless
Water Solubility 40 g/L (20 ºC)
Sensitive Air Sensitive
BRN 506259
InChIKeyMKIJJIMOAABWGF-UHFFFAOYSA-N
CAS DataBase Reference2365-48-2(CAS DataBase Reference)
NIST Chemistry ReferenceAcetic acid, mercapto-, methyl ester(2365-48-2)
EPA Substance Registry SystemAcetic acid, mercapto-, methyl ester (2365-48-2)
Safety Information
Hazard Codes Xn,T
Risk Statements 10-20/22-36/37/38-25
Safety Statements 26-36/37-45-36/37/39-28A
RIDADR UN 1992 3/PG 3
WGK Germany 1
RTECS AI7350000
TSCA Yes
HazardClass 3
PackingGroup III
HS Code 29309070
Hazardous Substances Data2365-48-2(Hazardous Substances Data)
MSDS Information
ProviderLanguage
Methyl mercaptoacetate English
SigmaAldrich English
ACROS English
ALFA English
Methyl thioglycolate Usage And Synthesis
Chemical PropertiesCLEAR COLOURLESS LIQUID
UsesMethyl Thioglycolate is an derivative of Thioglycolic Acid (T350760), an organic compound containing both a thiol and a carboxylic acid functional groups. Thioglycolic Acid and its derivatives are oft en used in organic synthesis as a nucleophile in thioglycolysis reactions and is also used as a S transfer agent for sulfonyl chloride synthesis. Methyl Thioglycolate have been studied for the its inf luence on neocarzinostatin activation and expression of DNA damage.
UsesMethyl thioglycolate was used in the preparation of 3-carbomethoxy-4- oxotetrahydrothiopyran, 2- and 4-carbomethoxy-3-oxotetrahydrothiophene. It is used to prepare methyl thioglycolate and aminoethanethiol conjugated gold nanorods.
General DescriptionMethyl thioglycolate reacts with nonprotein component of the antitumor antibiotic neocarzinostatin to form 1:1 adduct. It reacts with isothiocyanate to form Rhodanine.

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