Oleoyl chloride
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Oleoyl chloride
structure -
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CAS No:
112-77-6
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Formula:
C18H33ClO
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Chemical Name:
Oleoyl chloride
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Synonyms:
9-Octadecenoyl chloride,(9Z)-;Oleoyl chloride;9-Octadecenoyl chloride,(Z)-;(9Z)-9-Octadecenoyl chloride;Oleyl chloride;Oleic acid chloride;cis-9-Octadecenoyl chloride;(Z)-9-Octadecenoyl chloride;Oleic chloride;9-(Z)-Octadecen-1-oyl chloride
- Categories:
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CAS No:
Characteristics
17.07000
8.44
Liquid
0.9±0.1 g/cm3
158-159 °C @ Press: 0.05 Torr
>230 °F
1.464
−20°C
3.38E-05mmHg at 25°C
Safety Information
III
8
UN 3265 8/PG 2
3
34
26-36/37/39-45
C
P280-P305 + P351 + P338-P310
H314
|Danger|H314 (100%): Causes severe skin burns and eye damage [Danger Skin corrosion/irritation]|P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, and P501|Aggregated GHS information provided by 63 companies from 5 notifications to the ECHA C&L Inventory.
Oleoyl chloride Use and Manufacturing
Derived from the reaction of oleic acid and phosphorus trichloride. Put oleic acid into the reaction pot, slowly add phosphorus trichloride under stirring, and control the feeding temperature at 25-33°C. After the addition is completed, the temperature is increased to 55°C, and the lower phosphorous acid is separated after 4 hours of holding to obtain oleyl chloride.
Used as an intermediate in organic synthesis. A acylation reaction of 2-sulfo-4-aminoanisole with oleoyl chloride in drought can obtain a detergent LS (C25H40NNaO5S).
Intermediates
Oil and gas recovery
500,000 - 1,000,000 lb
All other basic organic chemical manufacturing|9-Octadecenoyl chloride, (9Z)-: ACTIVE
Computed Properties
Molecular Weight:300.9
XLogP3:8.3
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:15
Exact Mass:300.2219934
Monoisotopic Mass:300.2219934
Topological Polar Surface Area:17.1
Heavy Atom Count:20
Complexity:236
Undefined Bond Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
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