|Preferred IUPAC name
3D model (JSmol)
CompTox Dashboard (EPA)
|Molar mass||126.58 g/mol|
|Appearance||colorless to slightly yellow liquid|
|Melting point||−39 °C (−38 °F; 234 K)|
|Boiling point||179 °C (354 °F; 452 K)|
|very slightly soluble (0.05% at 20 °C)|
|Solubility||soluble in ethanol, ethyl ether, chloroform, CCl4 |
miscible in organic solvents
|Vapor pressure||1 mmHg (20 °C)|
Refractive index (nD)
|1.5415 (15 °C)|
|Safety data sheet||External MSDS|
|Flash point||67 °C (153 °F; 340 K)|
|585 °C (1,085 °F; 858 K)|
|Lethal dose or concentration (LD, LC):|
LD50 (median dose)
|1231 mg/kg (rat, oral)|
LC50 (median concentration)
|150 ppm (rat, 2 hr)|
80 ppm (mouse, 2 hr)
LCLo (lowest published)
|380 ppm (dog, 8 hr)|
|US health exposure limits (NIOSH):|
|TWA 1 ppm (5 mg/m3)|
|C 1 ppm (5 mg/m3) [15-minute]|
IDLH (Immediate danger)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
- C6H5CH3 + Cl2 → C6H5CH2Cl + HCl
In this way, approximately 100,000 tonnes are produced annually. The reaction proceeds by the free radical process, involving the intermediacy of free chlorine atoms. Side products of the reaction include benzal chloride and benzotrichloride.
Uses and reactions
Industrially, benzyl chloride is the precursor to benzyl esters which are used as plasticizers, flavorants, and perfumes. Phenylacetic acid, a precursor to pharmaceuticals, is produced from benzyl cyanide, which is generated by treatment of benzyl chloride with sodium cyanide. Quaternary ammonium salts, used as surfactants, are readily formed by alkylation of tertiary amines with benzyl chloride.
In organic synthesis, benzyl chloride is used for the introduction of the benzyl protecting group in reaction with alcohols, yielding the corresponding benzyl ether, carboxylic acids, and benzyl ester. Benzoic acid (C6H5COOH) can be prepared by oxidation of benzyl chloride in the presence of alkaline KMnO4:
- C6H5CH2Cl + 2 KOH + 2 [O] → C6H5COOK + KCl + H2O
Benzyl chloride may be used in the synthesis of amphetamine-class drugs, and for this reason, sales of benzyl chloride are monitored as a List II drug precursor chemical by the US Drug Enforcement Administration.
Benzyl chloride also reacts readily with metallic magnesium to produce a Grignard Reagent. It is preferable over benzyl bromide for the preparation of this reagent, since the reaction of the bromide with magnesium tends to form the Wurtz-coupling product 1,2-diphenylethane.
Benzyl chloride is an alkylating agent. Indicative of its high reactivity (relative to alkyl chlorides), benzyl chloride reacts with water in a hydrolysis reaction to form benzyl alcohol and hydrochloric acid. In contact with mucous membranes, hydrolysis produces hydrochloric acid. Thus, benzyl chloride is a lachrymator and has been used in chemical warfare. It is also very irritating to the skin.
It is classified as an extremely hazardous substance in the United States as defined in Section 302 of the U.S. Emergency Planning and Community Right-to-Know Act (42 U.S.C. 11002), and is subject to strict reporting requirements by facilities which produce, store, or use it in significant quantities.
- NIOSH Pocket Guide to Chemical Hazards. "#0053". National Institute for Occupational Safety and Health (NIOSH).
- "Benzyl chloride". Immediately Dangerous to Life and Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH).
- "Chlorinated Hydrocarbons", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, doi:10.1002/14356007.a06_233.pub2
- Furniss, B. S.; Hannaford, A. J.; Smith, P. W. G.; Tatchell, A. R. (1989), Vogel's Textbook of Practical Organic Chemistry (5th ed.), Harlow: Longman, p. 864, ISBN 0-582-46236-3.
- Henry Gilman and W. E. Catlin (1941). "n-Propylbenzene". Organic Syntheses.; Collective Volume, 1, p. 471
- "40 C.F.R.: Appendix A to Part 355—The List of Extremely Hazardous Substances and Their Threshold Planning Quantities" (PDF) (July 1, 2008 ed.). Government Printing Office. Retrieved October 29, 2011.
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