ISOBUTYRYL CHLORIDE

PRODUCT IDENTIFICATION
CAS NO. 79-30-1

ISOBUTYRYL CHLORIDE

EINECS NO. 201-194-1
FORMULA (CH3)2CHCOCl
MOL WT. 106.55
H.S. CODE 2915.90

TOXICITY

  
SYNONYMS 2-Methylpropionyl chloride; Chloroisopropyl ketone;
2-Methylpropanoyl chloride; alpha-Methylpropionyl chloride;  Dimethylacetyl chloride; Isobutanoyl chloride; Isobutyric acid chloride; Isobutyroyl chloride;

SMILES

 

CLASSIFICATION

 

PHYSICAL AND CHEMICAL PROPERTIES
PHYSICAL STATE

Clear to slightly yellow fuming liquid

MELTING POINT -90 C
BOILING POINT

92 C

SPECIFIC GRAVITY 1.1
SOLUBILITY IN WATER Rapidly hydrolysis
pH

 

VAPOR DENSITY  

AUTOIGNITION

325 C

REFRACTIVE INDEX

 1.4073

NFPA RATINGS

 Health: 3 Flammability: 3 Reactivity: 2
FLASH POINT 9 C
STABILITY Stable under ordinary conditions. but will fume when exposed to atmospheric moisture to form HCl and acetic acid.

DESCRIPTION AND APPLICATIONS
Acid chlorides are used as very reactive intermediates to prepare carboxylic acid derivatives including anhydrides, esters and amides because of the two strong electron withdrawing chlorine and oxygen on the carbonyl compound, and positive charge carbon accordingly. It is easy for a weak nucleophile to attack the carbon. Acid chlorides are also reactive with Gilman reagents to prepare large molecules from smal ones by replacing the halides with an organic group.  Isobutyryl Chloride is used in agrochemicals and pharmaceuticals manufacturing. It is also used as an intermediate for dyes, textile auxiliaries, peroxide compounds.
SALES SPECIFICATION

APPEARANCE

Clear liquid

ASSAY

99.0% min

ISOBUTANOIC ACID

0.5% max

COLOR

30 max, Hazen

TRANSPORTATION
PACKING 250kgs in drum
HAZARD CLASS 3 (Packing group: II)
UN NO. 2395
OTHER INFORMATION
Hazard Symbols: F C, Risk Phrases: 11-35, Safety Phrases: 16-23-26-28A-36-37-45

GENERAL DESCRIPTION OF ACYL HALIDE
Acyl is a radical formed from an organic acid by removal of a hydroxyl group. The general formula of acyl compound is RCO-. Acyl halide is one of a large group of organic substances containing the halocarbonyl group, have the general formula RCO·X, where X is a halogen atom (fluorine, chlorine, bromine, iodine, and astatine) and R may be aliphatic, alicyclic, aromatic, and H etc. In substitutive chemical nomenclature, their names are formed by adding '-oyl' as a suffix to the name of the parent compound; ethanoyl chloride, CH3COCl, is an example. The terms acyl and aroyl halides refer to aliphatic or aromatic derivatives, respectively. Acyl halides are made by replacing the -OH group in carboxylic acids by halogen using halogenating agents. They react readily with water, alcohols, and amines and are widely used in organic synthetic process whereby the acyl group is incorporated into the target molecules by substitution of addition-elimination sequence called acylation reaction.  Acylation reaction involves substitution by an electron donor (nucleophile) at the electrophilic carbonyl group (C=O). Common nucleophiles in the acylation reaction are aliphatic and aromatic alcohols, both of which give rise to esters and amines (RNH2) which give amides. The carboxylic acid (X = OH) itself can function as an acylating agent when it is protonated by a strong acid catalyst as in the direct esterification of an alcohol. Two common acylation agents, with the general formula RCOX, are acid halides (X = halogen atom) and anhydrides (X = OCOR). Schotten-Baumann reaction is an acylation reaction that uses an acid chloride in the presence of dilute alkali to acylate the hydroxyl and amino group of organic compounds. There are also other acylating agents. Acyl halide compounds are used as an intermediate for agrochemicals and pharmaceuticals, dyes, and peroxide compounds as well as textile auxiliaries, emulsifiers.

PRICE INFORMATION