2-Ethylhexyl mercaptoacetate

2-Ethylhexyl mercaptoacetate Basic information
Product Name:2-Ethylhexyl mercaptoacetate
Synonyms:2-Ethylhexylmercaptoacetat;2-Ethylhexyl 2-mercaptoacetate;2-Mercaptoacetic acid 2-ethylhexyl ester;Thioglycollic acid 2-ethylhexyl ester;2-ethylhexyl 2-sulfanylethanoate;Thioglycolic Acid 2-Ethylhexyl Ester Mercaptoacetic Acid 2-Ethylhexyl Ester Octyl Thioglycolate Thioglycolic Acid Octyl Ester 2-Ethylhexyl Mercaptoacetate;Acetic acid,2-Mercapto-, 2-ethylhexyl ester;2-Ethylhexyl thioglycolate >=95.0% (GC)
CAS:7659-86-1
MF:C10H20O2S
MW:204.33
EINECS:231-626-4
Product Categories:Industrial/Fine Chemicals;bc0001
Mol File:7659-86-1.mol
2-Ethylhexyl mercaptoacetate Structure
2-Ethylhexyl mercaptoacetate Chemical Properties
Boiling point 255-260 °C (lit.)
density 0.972 g/mL at 20 °C (lit.)
vapor pressure 3.6Pa at 25℃
refractive index n20/D 1.461
Fp 136 °C
storage temp. Store below +30°C.
solubility 4.73mg/l
pka7.95±0.10(Predicted)
form Oil
color Colourless
Water Solubility 4.73mg/L at 20℃
BRN 9047474
InChIKeyOWHSTLLOZWTNTQ-UHFFFAOYSA-N
LogP4.7 at 20℃
CAS DataBase Reference7659-86-1(CAS DataBase Reference)
EPA Substance Registry SystemAcetic acid, mercapto-, 2-ethylhexyl ester (7659-86-1)
Safety Information
Hazard Codes Xn
Risk Statements 10-20/22-36/37/38
Safety Statements 26-36/37
RIDADR UN 3272 3/PG 3
WGK Germany 3
RTECS AI7255000
HazardClass 3.2
PackingGroup III
HS Code 29309070
MSDS Information
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2-Ethylhexyl mercaptoacetate English
SigmaAldrich English
2-Ethylhexyl mercaptoacetate Usage And Synthesis
UsesThioglycolic Acid 2-Ethylhexyl Ester is a chain transfer agent that is useful for preparing latex with flame retardancy.
Uses2-Ethylhexyl mercaptoacetate can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development processes and chemical production processes.
Synthesis52.1 g (0.2 mol) of N,N'-diphenyl-1,4-phenylenediamine and 81.7 g (0.4 mol) of 2-ethylhexyl thioglycollate in 200 ml of ethanol are initially placed in a 750 ml sulfonation flask equipped with a propeller stirrer, and are heated to reflux temperature. 36.7 g (0.44 mol) of 36% aqueous formaldehyde are added dropwise in the course of 2 hours, and the reaction mixture is then boiled under reflux for 16 hours. The batch is concentrated on a rotary evaporator, and the residue is then dried at 80° C. for 2 hours under a high vacuum. 127.3 g (91.8% of theory) of a dark brown oil are obtained. Analysis: Calculated; C 69.33%, H 8.15%, N 4.04%, S 9.25%, Found; C 70.2%, H 8.13%, N 3.96%, S 9.29%.
2-Ethylhexyl mercaptoacetate Preparation Products And Raw materials
Preparation ProductsMethyltin mercaptide-->ISOOCTYL THIOGLYCOLATE
VINYL ESTER RESIN Tiamulin fumarate Calcium thioglycolate SUCCINIC ACID DI-(ETHYLHEXYL)-ESTER 2-SULFONIC ACID POTASSIUM SALT AURORA 14986 2-ethylhexyl [[[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl]methyl]thio]acetate DI-2-ETHYLHEXYL THIODIGLYCOLATE antimony(3+) tris[2-(isooctyloxy)-2-oxoethanethiolate] SODIUM-1,2-BIS-(1-D2-2-ETHYL-HEXYL)-SULPHOSUCCINATE 2-ETHYLHEXYLTHIOCYANOACETATE Isooctyl thioglycolate butyl tin (1R,2S,5R)-Menthyl-(2R,5S)-5-(4-amino-2-oxo-2H-pyrimidin-1-yl)-[1,3]oxathiolane-2-carboxylic acid migraleve POTASSIUM THIOGLYCOLATE 2-(2-ISOPROPYL-5-METHYL-CYCLOHEXYLOXYCARBONYLMETHYLSULFANYL)-BENZOIC ACID AcidEster LUTEINESTER ISOBORNYL THIOCYANOACETATE

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