Acetyl chloride manufacturers and suppliers

Acetyl chloride suppliers

Properties

Melting point:: -112 °C

Boiling point:: 52 °C(lit.)

Density: 1.104 g/mL at 25 °C(lit.)

vapor density: 2.7 (vs air)

vapor pressure: 11.69 psi ( 20 °C)

refractive index: n20/D 1.389(lit.)

Flash point:: 40 °F

storage temp.: Store below +15°C.

solubility: Miscible with acetone, chloroform, glacial acetic acid, petroleum ether, ether and benzene.

form: Liquid

color: Clear colorless

Specific Gravity: approximate 1.11

Odor: Strong pungent odor

explosive limit: 7.3-19%(V)

Water Solubility: Decomposes violently in water

Sensitive: Moisture Sensitive

Merck: 14,85

BRN: 605303

Dielectric constant: 16.9（2℃）

Stability:: Stability Highly flammable. Reacts violently with DMSO, water, lower alcohols, and amines to generate toxic fumes. May form an explosive mixture with air. Note low flash point. Incompatible with water, alcohols, amines, strong bases, strong oxidizing agents, most common metals.

InChIKey: WETWJCDKMRHUPV-UHFFFAOYSA-N

Safety Information

Symbol(GHS): GHS02,GHS05

Signal word: Danger

Hazard statements: H225-H314

Precautionary statements: P210-P233-P240-P280-P303+P361+P353-P305+P351+P338

Hazard Codes: F,C,Xn

Risk Statements: 11-14-34-40-36/38

Safety Statements: 9-16-26-45-1/2-36/37

RIDADR: UN 1717 3/PG 2

WGK Germany: 1

RTECS: AO6390000

F: 3

Autoignition Temperature: 390 °C DIN 51794

TSCA: Yes

HazardClass: 3

PackingGroup: II

HS Code: 29159080

Use

A colorless, fuming liquid with a pungent odor. Density 9.2 lb / gal. Flash point 40F. Vapor, which is heavier than air, irritates the eyes and mucous membranes. Corrosive to metals and tissue. Acetyl chloride, CH30CCI, can be prepared by treatment ofacetic acid with various reagents, such as PCl3 SOCl2 or COCI2. It can be prepared by chlorination of acetic anhydride in several different ways, by reaction of methyl chloride with carbon monoxide in the presence of catalysts, by reaction ofketene with HCI, or by partial hydrolysis of 1, 1, l-trichloroethane, Acetyl chloride hydrolyzes in the presence of water to give acetic acid. It reacts with ammonia and amines to give acetamides. Reaction with alcohols gives the corresponding acetate esters. Acetyl chloride will add across unsaturated bonds in the presence ofsuitable catalysts to give halogenated ketones.

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