2-Ethylhexyl thioglycolate

Base Information

• Chemical Name: 2-Ethylhexyl thioglycolate
• CAS No.: 7659-86-1
• Deprecated CAS: 32885-07-7
• Molecular Formula: C10H20O2S
• Molecular Weight: 204.334
• Hs Code.: H 2COOC8H17
• European Community (EC) Number: 231-626-4
• UNII: X6P51ASB6H
• DSSTox Substance ID: DTXSID4027656
• Nikkaji Number: J150.356A
• Wikidata: Q27887386
• ChEMBL ID: CHEMBL1869371
• Mol file: 7659-86-1.mol

Synonyms:thioglycolic acid-2-ethylhexyl esters

Chemical Property of 2-Ethylhexyl thioglycolate

Chemical Property:

• Appearance/Colour: Clear liquid
• Vapor Pressure: 3.6Pa at 25℃
• Melting Point: -31oC
• Refractive Index: n20/D 1.461
• Boiling Point: 270.9 °C at 760 mmHg
• PKA: 7.95±0.10(Predicted)
• Flash Point: 137.4 °C
• PSA: 65.10000
• Density: 0.972 g/cm³
• LogP: 2.67580
• Storage Temp.: Store below +30°C.
• Solubility.: 4.73mg/l
• Water Solubility.: 4.73mg/L at 20℃
• XLogP3: 3.6
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 8
• Exact Mass: 204.11840105
• Heavy Atom Count: 13
• Complexity: 137

Purity/Quality:

99% ^*data from raw suppliers

ThioglycolicAcid2-EthylhexylEster ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xn
• Hazard Codes: Xn
• Statements: 10-20/22-36/37/38
• Safety Statements: 26-36/37

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCC(CC)COC(=O)CS
• Uses: 2-Ethylhexyl mercaptoacetate can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development processes and chemical production processes. Thioglycolic Acid 2-Ethylhexyl Ester is a chain transfer agent that is useful for preparing latex with flame retardancy.

Technology Process of 2-Ethylhexyl thioglycolate

There total 1 articles about 2-Ethylhexyl 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:

→ mercaptoacetic acid 2-ethylhexyl ester (7659-86-1)

Guidance literature:

Reference yield: 98.0%

n-octyltin trichloride (3091-25-6) + mercaptoacetic acid 2-ethylhexyl ester (7659-86-1) → octyltin tris(isooctyl thioglycollate) (27107-89-7,64685-80-9)

Guidance literature:

With sodium hydroxide; In water; at 50 ℃; for 2h; Product distribution / selectivity;

Reference yield: 97.6%

mercaptoacetic acid 2-ethylhexyl ester (7659-86-1) → 2-Ethylhexyl N,N-diphenylaminomethylthioacetate

Guidance literature:

With diphenylamine; paraformaldehyde; In water; toluene;

Downstream raw materials:

2-ethylhexyl 2-(3,5-di-tert-butyl-4-hydroxybenzylthio)acetate

Cr(C₄₄H₂₈N₄)(SCH₂COOCH₂CH(C₂H₅)C₄H₉)2^(1-)

(C₆H₅CH₂OC(O)CH₂CH₂)2Sn(SCH₂CO₂CH₂CH(C₂H₅)(CH₂)3CH₃)2

di(2-butoxycarbonylethyl)tin S,S'-bis-(2-ethylhexyl thioglycolate)

Refernces