Butyryl chloride
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Names | |
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Preferred IUPAC name
Butanoyl chloride | |
Other names
Butyryl chloride
n-Butyryl chloride Butanoyl chloride | |
Identifiers | |
3D model (JSmol)
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ChEMBL | |
ChemSpider | |
EC Number |
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PubChem CID
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UNII | |
UN number | 2353 |
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Properties | |
C4H7ClO | |
Molar mass | 106.55 g·mol−1 |
Appearance | colorless liquid |
Odor | pungent |
Density | 1.033 g/cm3 |
Melting point | −89 °C (−128 °F; 184 K) |
Boiling point | 102 °C (216 °F; 375 K) |
decomposition | |
Solubility | miscible with ether |
-62.1·10−6 cm3/mol | |
Refractive index (nD)
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1.412 |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
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Reacts violently with water, flammable, corrosive |
GHS labelling: | |
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Danger | |
H225, H314 | |
P210, P233, P240, P241, P242, P243, P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P370+P378, P403+P235, P405, P501 | |
NFPA 704 (fire diamond) | <imagemap>
File:NFPA 704.svg|80px|alt=NFPA 704 four-colored diamond poly 150 150 300 300 150 450 0 300 Health 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gas poly 300 0 450 150 300 300 150 150 Flammability 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g. gasoline poly 450 150 600 300 450 450 300 300 Instability 2: Undergoes violent chemical change at elevated temperatures and pressures, reacts violently with water, or may form explosive mixtures with water. E.g. white phosphorus poly 300 300 450 450 300 600 150 450 Special hazards (white): no code desc none </imagemap> |
Flash point | 21.7 °C (71.1 °F; 294.8 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Butyryl chloride is an organic compound with the chemical formula CH3CH2CH2C(O)Cl. It is a colorless liquid with a unpleasant odor. Butyryl chloride is soluble in organic solvents, but it reacts readily with water and alcohols. It is usually produced by chlorination of butyric acid.[1]
Reactions
Like related acyl chlorides, butyryl chloride hydrolyzes readily:
- CH3CH2CH2C(O)Cl + H2O → CH3CH2CH2CO2H + HCl
Alcohols react to give esters:
- CH3CH2CH2C(O)Cl + ROH → CH3CH2CH2CO2R + HCl
Amines react to give amides:
- CH3CH2CH2C(O)Cl + R2NH → CH3CH2CH2C(O)NR2 + HCl
Derivatives of butyryl chloride are used in manufacturing pesticides, pharmaceuticals, perfume fixative, polymerization catalyst, and dyestuffs. Butyryl chloride is also commonly used as an intermediate for organic synthesis for the preparation of pharmaceuticals, agrochemicals, dyes, esters, and peroxide compounds.[2]
Safety
Butyryl chloride is flammable and fumes in air, releasing hydrogen chloride.
References
- ^ Helferich, B.; Schaefer, W. (1929). "n-Butyryl Chloride". Org. Synth. 9: 32. doi:10.15227/orgsyn.009.0032.
- ^ "N-BUTYRYL CHLORIDE (BUTANOYL CHLORIDE)". chemicalland21.com. Retrieved 2023-02-20.