In organic synthesis, benzyl chloride is used to introduce the benzyl protecting group in reaction with alcohols, yielding the corresponding benzyl ether, carboxylic acids, and benzyl ester. However, it is not complete retard, meaning that the pre polymer is not stable at the storage. Last updated on Aug 4, 2020. Benzoyl chloride, 4-methyl-p-Methylbenzoyl chloride. 2011, volume 88, pp. 398. If you have an animal bite or a deep puncture wound. It is primarily used in the production of peroxides. Talk with the doctor. Tell your doctor and pharmacist about all of your drugs (prescription or OTC, natural products, vitamins) and health problems. Use with care in a child younger than 2 years of age. Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances. Benzoyl chloride is produced from benzotrichloride using either water or benzoic acid:[1], As with other acyl chlorides, it can be generated from the parent acid and other chlorinating agents phosphorus pentachloride, thionyl chloride, or oxalyl chloride. provides accurate and independent information on more than 24,000 prescription drugs, over-the-counter medicines and natural products. Do not wash your hands after use if putting this on your hand. Contents. Benzoyl chloride EC Number: 202-710-8 EC Name: Benzoyl chloride CAS Number: 98-88-4 Molecular formula: C7H5ClO IUPAC Name: benzoyl chloride . [6], InChI=1S/C7H7Cl/c8-6-7-4-2-1-3-5-7/h1-5H,6H2, InChI=1/C7H7Cl/c8-6-7-4-2-1-3-5-7/h1-5H,6H2, Except where otherwise noted, data are given for materials in their, Emergency Planning and Community Right-to-Know Act, National Institute for Occupational Safety and Health, Ullmann's Encyclopedia of Industrial Chemistry, "40 C.F.R. Use a missed dose as soon as you think about it. It is mainly useful for the production of peroxides but is generally useful in other areas such as in the preparation of dyes, perfumes, pharmaceuticals, and resins. Throw away unused or expired drugs. Benzyl chloride reacts with aqueous sodium hydroxide to give dibenzyl ether. [6] With carbanions, it serves again as a source of "PhCO+". Benzoyl chloride, also known as benzenecarbonyl chloride, is an organochlorine compound with the formula C6H5COCl. It was first prepared by treatment of benzaldehyde with chlorine. Use on your skin only. If you think there has been an overdose, call your poison control center or get medical care right away. Use with care in a child younger than 2 years of age. Create . If it is close to the time for your next dose, skip the missed dose and go back to your normal time. Available for Android and iOS devices. [4][5], It undergoes the Friedel-Crafts acylation with aromatic compounds to give the corresponding benzophenones and related derivatives. [6] With carbanions, it serves again as a source of "PhCO+". It is classified as an extremely hazardous substance in the United States as defined in Section 302 of the U.S. If you have an allergy to benzalkonium chloride or any other part of benzalkonium chloride. Synth. [7], Benzoyl peroxide, a common reagent in polymer chemistry, is produced industrially by treating benzoyl chloride with hydrogen peroxide and sodium hydroxide:[8], InChI=1S/C7H5ClO/c8-7(9)6-4-2-1-3-5-6/h1-5H, InChI=1/C7H5ClO/c8-7(9)6-4-2-1-3-5-6/h1-5H, Except where otherwise noted, data are given for materials in their.

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