Oleoyl Chloride

CAS No. 112-77-6 Content 97% Packing 180kg/drum 850kg/IBC  Names and Identifiers Name oleoyl chloride Synonyms NSC 97299 oleoyl chloride OLEOYL CHLORIDE Oleoyl chloride OLEIC ACID CHLORIDE Ole...

Category:Paint chemicals

Introduction

CAS No. 112-77-6

Content 97%

Packing 180kg/drum 850kg/IBC

 Names and Identifiers

Name oleoyl chloride
Synonyms NSC 97299
oleoyl chloride
OLEOYL CHLORIDE
Oleoyl chloride
OLEIC ACID CHLORIDE
Oleic acid chloride
OCTADECENOYLCHLORIDE
9-OCTADECENOYL CHLORIDE
octadec-9-enoyl chloride
(z)-9-octadecenoylchlorid
(9Z)-1-chlorooctadec-9-ene
(9Z)-octadec-9-enoyl chloride
9-Octadecenoyl chloride, (9Z)-
DELTA 9 CIS-OCTADECENOYL CHLORIDE
9-Octadecenoyl chloride, (Z)- (9CI)
CAS 112-77-6
EINECS 204-005-0
InChI InChI=1/C18H35Cl/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19/h9-10H,2-8,11-18H2,1H3/b10-9-

112-77-6 – Physico-chemical Properties

Molecular Formula C18H33ClO
Molar Mass 300.91
Density 0.91 g/mL at 25 °C (lit.)
Boling Point 193 °C/4 mmHg (lit.)
Flash Point >230°F
Solubility Chloroform (Slightly)
Vapor Presure 3.38E-05mmHg at 25°C
Appearance Oil
Specific Gravity 0.912
Color Clear Colourless to Pale Beige
BRN 1211748
Storage Condition −20°C
Stability Moisture Sensitive
Sensitive Sensitive to humidity
Refractive Index n20/D 1.463(lit.)
MDL MFCD00134332
Physical and Chemical Properties Liquid. Boiling point 200 ℃(1.46kPa),175-180 ℃(0.4kPa), relative density 0.912, refractive index 1.4623.

112-77-6 – Risk and Safety

Hazard Symbols C – Corrosive
Risk Codes 34 – Causes burns
Safety Description S26 – In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S36/37/39 – Wear suitable protective clothing, gloves and eye/face protection.
S45 – In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.)
UN IDs UN 3265 8/PG 2
WGK Germany 3
HS Code 29161900
Hazard Class 8
Packing Group III

Reference Information

application oleoyl chloride is a widely used organic synthesis intermediate, which can react with alcohols, phenols, amines and other compounds to synthesize various surfactants At the same time, it can also be directly applied to wool spinning, silk, synthetic fiber, printing and dyeing, machinery industries and other industries.
Use Used as an intermediate in organic synthesis. The detergent LS(C25H40NNaO5S) can be obtained by acylation of 2-sulfo-4-aminoanisole in drought with oleoyl chloride.
Production method is obtained by the reaction of oleic acid and phosphorus trichloride. Put the oleic acid into the reaction pot, slowly add phosphorus trichloride under stirring, and control the feeding temperature at 25-33 ℃. After adding, the temperature is raised to 55 ℃, and the lower phosphorous acid is removed after keeping the temperature for 4 hours to obtain oleyl chloride.

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