Ethyl thioglycolate

Base Information Edit

Chemical Name:Ethyl thioglycolate
CAS No.:623-51-8
Molecular Formula:C4H8O2S
Molecular Weight:120.172
Hs Code.:29309090
European Community (EC) Number:210-800-3
NSC Number:8834
UNII:Z5SD8DD6CP
DSSTox Substance ID:DTXSID8049337
Nikkaji Number:J49.275B
Wikidata:Q27295042
ChEMBL ID:CHEMBL3181965
Mol file:623-51-8.mol

Synonyms:ethyl 2-sulfanylacetate

Suppliers and Price of Ethyl thioglycolate

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
Ethyl2-Mercaptoacetate
10g
$ 95.00

TRC
Ethyl2-Mercaptoacetate
50 g
$ 195.00

TRC
Ethyl2-Mercaptoacetate
100 g
$ 330.00

TCI Chemical
Ethyl Thioglycolate >97.0%(GC)
500g
$ 231.00

TCI Chemical
Ethyl Thioglycolate >97.0%(GC)
25g
$ 28.00

SynQuest Laboratories
Ethyl thioglycolate
5 g
$ 18.00

Sigma-Aldrich
Ethyl thioglycolate 97%
25g
$ 83.20

Sigma-Aldrich
Ethyl thioglycolate 97%
5g
$ 30.60

Frontier Specialty Chemicals
Ethyl2-mercaptoacetate 99%
100g
$ 30.00

Frontier Specialty Chemicals
Ethyl2-mercaptoacetate 99%
500g
$ 110.00

Total 99 raw suppliers

Chemical Property of Ethyl thioglycolate Edit

Chemical Property:

Appearance/Colour:colourless liquid
Vapor Pressure:2.7mmHg at 25°C
Melting Point:-80 °C
Refractive Index:n20/D 1.457(lit.)
Boiling Point:157.8 °C at 760 mmHg
PKA:pK1:7.95(SH) (25°C)
Flash Point:47.8 °C
PSA：65.10000
Density:1.072 g/cm³
LogP:0.47930
Storage Temp.:Flammables area
Sensitive.:Air Sensitive
Water Solubility.:Not miscible or difficult to mix in water.
XLogP3:0.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:120.02450067
Heavy Atom Count:7
Complexity:62.7

Purity/Quality:

99% ^*data from raw suppliers

Ethyl2-Mercaptoacetate ^*data from reagent suppliers

Safty Information:

Pictogram(s): T
Hazard Codes:T
Statements: 10-25-36/38
Safety Statements: 26-36/37/39-45

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Chemical Classes:Other Classes -> Esters, Other
Canonical SMILES:CCOC(=O)CS
Uses It finds its application in the reaction of the dilithio-derivative with an aldehyde, followed by conversion to the episulfide by reaction with ethyl chloroformate, and desulfurization with triethyl phosphite, leads to the (E)-2-alkenoic acid with high stereoselectivity. It is used as depilatories, hair straightening agent, hair waving agent, and reducing agent in cosmetic industry.

Technology Process of Ethyl thioglycolate

There total 30 articles about Ethyl thioglycolate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 72.0%