Propionyl chloride Chemical Properties

Melting point:

-94 °C

Boiling point:

77-79 °C (lit.)

Density 

1.059 g/mL at 25 °C (lit.)

vapor density 

3.2 (vs air)

vapor pressure 

106 hPa (20 °C)

refractive index 

n20/D 1.404(lit.)

Flash point:

53 °F

storage temp. 

Store below +30°C.

form 

Liquid

color 

Clear

PH Range

<7.0

explosive limit

3.6-11.9%(V)

Water Solubility 

REACTS

FreezingPoint 

-94℃

Sensitive 

Moisture Sensitive

Merck 

14,7828

BRN 

385632

Exposure limits

ACGIH: TWA 0.1 ppm
OSHA: TWA 0.1 ppm(0.4 mg/m3)
NIOSH: IDLH 2 ppm; TWA 0.1 ppm(0.4 mg/m3); Ceiling 0.2 ppm(0.8 mg/m3)

InChIKey

RZWZRACFZGVKFM-UHFFFAOYSA-N

CAS DataBase Reference

79-03-8(CAS DataBase Reference)

NIST Chemistry Reference

Propanoyl chloride(79-03-8)

EPA Substance Registry System

Propanoyl chloride (79-03-8)

Safety Information

Hazard Codes 

F,C

Risk Statements 

11-14-34-20/22

Safety Statements 

9-16-26-45

RIDADR 

UN 1815 3/PG 2

WGK Germany 

1

RTECS 

UG6657000

Autoignition Temperature

270 °C

TSCA 

Yes

HazardClass 

3

PackingGroup 

II

HS Code 

29051900

HS Code 

29399990

Hazardous Substances Data

79-03-8(Hazardous Substances Data)

Toxicity

LD50 orally in Rabbit: 823 mg/kg

MSDS

• Language:English Provider:Propionyl chloride
• Language:English Provider:SigmaAldrich
• Language:English Provider:ACROS
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Propionyl chloride Usage And Synthesis

Chemical Properties

Propionyl chloride is a colorless to light yellow, volatile, and readily flammable liquid, whose vapors hydrolyze in moist air. It is corrosive, lachrymatory, and has a strongly pungent odor. With water and lower alcohols it reacts vigorously under solvolysis to give the acid or ester. It is used for the introduction of the propionyl group and for the synthesis of propionate esters because of its high reactivity.

Uses

Propionyl chloride is used as an intermediate in the production of agrochemicals and pharmaceuticals. It serves as an intermediate for dyes, textile auxiliaries and peroxide compounds. It acts as a crop protecting agent.

Preparation

Propionyl chloride is synthesized by reacting propionic acid with phosphorus trichloride at 40-50°C for 1h, cooling, standing, separating and distilling to obtain the product.
CH3CH2COOH+PCl3→CH3CH2COCl+HOPCl2
Propionyl chloride is produced industrially by treatment of propionic acid with phosgene or thionyl chloride. The reaction occurs at ca. 50°C in the liquid phase in the presence of dialkylformamides. The product is then separated by distillation.
CH3CH2CO2H + COCl2 → CH3CH2COCl + HCl + CO2
Propionyl chloride can also be obtained by the reaction of propionic acid with PCl5.

Application

Propionyl chloride is used for the introduction of the propionyl group and for the synthesis of propionate esters because of its high reactivity. It is an chemical intermediate in the preparation of various propionic acid derivatives, It can also be used:
To convert anisole to 4-methoxypropiophenone and 2-methoxynaphthalene to 1-propio-2-methoxynaphthalene in the presence of Indium(III) chloride (InCl3) impregnated mesoporous Si-MCM-41 catalyst.
For chlorination in the presence of sulfuryl chloride and peroxides to form α-chloropropionyl chloride and β-chloropropionyl chloride.
In reaction with (hydroxypropyl)cellulose to form the propanoate ester, [(propionyloxy)propyl]cellulose.

General Description

Propionyl chloride appears as a colorless liquid with a pungent odor. Corrosive and very irritating to skin and eyes. Used to make other chemicals.

General Description

Propionyl chloride is an important chemical intermediate used to synthesize various propionic acid derivatives.

Air & Water Reactions

Highly flammable. Propionyl chloride reacts vigorously or violently with water to form propionic acid and hydrochloric acid [Merck 11th ed. 1989].

Reactivity Profile

Acid halides, such as Propionyl chloride, are water reactive; some are violently reactive. They are incompatible with strong oxidizing agents, alcohols, amines, and alkali. May react vigorously or explosively if mixed with diisopropyl ether or other ethers in the presence of trace amounts of metal salts [J. Haz. Mat., 1981, 4, 291].

Hazard

Strong irritant to skin.

Health Hazard

May cause toxic effects if inhaled or ingested/swallowed. Contact with substance may cause severe burns to skin and eyes. Fire will produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution.

Fire Hazard

Propionyl chloride is a flammable/combustible material.. May be ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.

Flammability and Explosibility

Highly flammable

Safety Profile

A corrosive irritant to skin, eyes, and mucous membranes. Dangerous fire hazard when exposed to heat or flame; can react vigorously with oxidizing materials. Reacts with water or steam to produce toxic and corrosive fumes. Exothermic reaction with diisopropyl ether produces much gas. The reaction may be dangerous if confmed. To fight fire, use CO2, dry chemical; do not use water. When heated to decomposition it emits lughly toxic fumes of Cl-. See also HYDROCHLORIC ACID.

Propionyl chloride(79-03-8)Related Product Information

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• Calcium chloride
• Mepiquat chloride
• Ammonium chloride
• Polyvinyl chloride
• Sodium chloride
• Propionic acid
• Acetyl chloride
• Methylene Chloride
• 2-Chloropropionyl chloride
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• 4-Butoxyphenol
• 1-Chlorocarbonyl-1-methylethyl acetate
• Propionyl chloride, 3-chloro-
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• Methacryloyl chloride
• Malonyl chloride