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Propionyl chloride

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Propionyl chloride Basic information
Product Name:Propionyl chloride
Synonyms:PROPIONYL CHLORIDE;Propanoic acid chloride;Propionyl chloride, 98% 500GR;Propionic chloride;Propionylchloride,98%;Propanoylchlorid;Propionyl Chloride Factory Price;Propionyl Chloride CAS 79-03-8
CAS:79-03-8
MF:C3H5ClO
MW:92.52
EINECS:201-170-0
Product Categories:Acid Halides;Organics;Acid Halides;Carbonyl Compounds;Organic Building Blocks;organic synthesis material;Building Blocks;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;API Intermediate;79-03-8;K00001
Mol File:79-03-8.mol
Propionyl chloride Structure
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.)
Fp 53 °F
storage temp. Store below +30°C.
form Liquid
color Clear
PH Range<7.0
explosive limit3.6-11.9%(V)
Water Solubility REACTS
FreezingPoint -94℃
Sensitive Moisture Sensitive
Merck 14,7828
BRN 385632
Exposure limitsACGIH: 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)
InChIKeyRZWZRACFZGVKFM-UHFFFAOYSA-N
CAS DataBase Reference79-03-8(CAS DataBase Reference)
NIST Chemistry ReferencePropanoyl chloride(79-03-8)
EPA Substance Registry SystemPropanoyl 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 Temperature270 °C
TSCA Yes
HazardClass 3
PackingGroup II
HS Code 29051900
HS Code 29399990
Hazardous Substances Data79-03-8(Hazardous Substances Data)
ToxicityLD50 orally in Rabbit: 823 mg/kg
MSDS Information
ProviderLanguage
Propionyl chloride English
SigmaAldrich English
ACROS English
ALFA English
Propionyl chloride Usage And Synthesis
Chemical PropertiesPropionyl 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.
UsesPropionyl 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.
ApplicationPropionyl 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.
PreparationPropionyl 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.
General DescriptionPropionyl chloride appears as a colorless liquid with a pungent odor. Corrosive and very irritating to skin and eyes. Used to make other chemicals.
Air & Water ReactionsHighly flammable. Propionyl chloride reacts vigorously or violently with water to form propionic acid and hydrochloric acid [Merck 11th ed. 1989].
Reactivity ProfileAcid 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].
HazardStrong irritant to skin.
Health HazardMay 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 HazardFlammable/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 ExplosibilityHighly flammable
Safety ProfileA 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.
Tag:Propionyl chloride(79-03-8) Related Product Information
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