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Oleoyl Chloride

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CAS No. 112-77-6

Content 97%

Packing 180kg/drum 850kg/IBC

 Names and Identifiers

Nameoleoyl chloride
SynonymsNSC 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)
CAS112-77-6
EINECS204-005-0
InChIInChI=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 FormulaC18H33ClO
Molar Mass300.91
Density0.91 g/mL at 25 °C (lit.)
Boling Point193 °C/4 mmHg (lit.)
Flash Point>230°F
SolubilityChloroform (Slightly)
Vapor Presure3.38E-05mmHg at 25°C
AppearanceOil
Specific Gravity0.912
ColorClear Colourless to Pale Beige
BRN1211748
Storage Condition−20°C
StabilityMoisture Sensitive
SensitiveSensitive to humidity
Refractive Indexn20/D 1.463(lit.)
MDLMFCD00134332
Physical and Chemical PropertiesLiquid. Boiling point 200 ℃(1.46kPa),175-180 ℃(0.4kPa), relative density 0.912, refractive index 1.4623.

112-77-6 – Risk and Safety

Hazard SymbolsC – Corrosive
Risk Codes34 – Causes burns
Safety DescriptionS26 – 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 IDsUN 3265 8/PG 2
WGK Germany3
HS Code29161900
Hazard Class8
Packing GroupIII

Reference Information

applicationoleoyl 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.
UseUsed 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 methodis 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.

Declaration: The products displayed on this website are intended exclusively for industrial applications or scientific research. They are not intended for medical, pharmaceutical, or food use. In accordance with applicable laws and regulations, purchasing organizations must hold valid qualifications and approvals.

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