98-88-4, EC Number 202-710-8. Copyright © 2017 ChemicalBook All rights reserved. Particle size distribution (Granulometry), Solubility in organic solvents / fat solubility, Stability in organic solvents and identity of relevant degradation products, Storage stability and reactivity towards container material, Biodegradation in water and sediment: simulation tests, Additional information on environmental fate and behaviour, Short-term toxicity to aquatic invertebrates, Long-term toxicity to aquatic invertebrates, Toxicity to aquatic algae and cyanobacteria, Toxicity to aquatic plants other than algae, Endocrine disrupter testing in aquatic vertebrates – in vivo, Toxicity to soil macroorganisms except arthropods, Endocrine disrupter mammalian screening – in vivo (level 3), Direct observations: clinical cases, poisoning incidents and other, Exposure related observations in humans: other data, Registrants / Suppliers - Ceased manufacture, Registration numbers - Ceased manufacture, Additional physico-chemical properties of nanomaterials, Toxicokinetics, metabolism and distribution. Please upgrade your Internet Explorer to a newer version. 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. Basic Red 9, Benzoyl chloride, 4-chloro-,Benzoyl chloride, p-chloro-, LD50 orally in Rabbit: 2460 mg/kg LD50 dermal Rabbit 790 mg/kg. Some of the manufacturers also produce acid chloride, and the production capacity is 10,000t. CAS No. Display Name: Benzoyl chloride EC Number: 202-710-8 EC Name: Benzoyl chloride CAS Number: 98-88-4 Molecular formula: C7H5ClO IUPAC Name: benzoyl chloride Benzoyl chloride for synthesis. Most of benzoyl chloride is used in the production of benzoyl peroxide, and secondly for the production of benzophenone, benzyl benzoate, benzyl cellulose. Benzoyl chloride is a useful acylating agent, preparation of ketones from organometallic compounds; It is mainly useful for t.... (File Format: Jpg, Gif, Png, PDF,Zip,Txt,doc or xls Max Size: 3MB), Lastest Price from Benzoyl chloride manufacturers, antiviral fungicide Benzoyl chloride 8619930501651, The Applications and Reactions of Benzoyl chloride, Absolute Configuration Determination (Exciton Chirality CD Method), Enantiomer Excess & Absolute Configuration Determination, Exciton Chirality CD Method (for Hydroxyl Groups), Hydroxyl Group Labeling Reagents for HPLC, Nucleosides, Nucleotides & Related Reagents, Protecting Agents for Hydroxyl and Amino Groups, Protecting Agents, Phosphorylating Agents & Condensing Agents, A-B, Puriss p.a. - Find MSDS or SDS, a COA, data sheets and more information. Benzoyl chloride is an important benzoyl and benzyl reagent. - Find MSDS or SDS, a COA, data sheets and more information. However, according to the 2003 survey, the profit is too low, because of the use of small polluting production line, while the use of polluting route is controlled by the government restrictions, and a further raw material price increases. This site is not fully supported in Internet Explorer 7 (and earlier versions). Benzyl chloride is prepared industrially by the gas-phase photochemical reaction of toluene with chlorine: Benzoyl chloride Melting point is-1.0 ℃, boiling point is 197.2 ℃, and the relative density is 1.212 (20 ℃), while a flash point is 72 ℃, and refractive index (n20) is 1.554. Used for dye intermediates, initiator, UV absorbers, rubber additives, medicine etc. Side products of the reaction include benzal chloride … All rights reserved, The mailbox will be used as the login user name and retrieve the password. Therefore most of the manufacturers stop the production. Further reaction with the acid chloride can also produce acid anhydride, and benzoic acid anhydride is the main purpose for acylation agents, which can also be used as a bleaching agent and flux of a component, as well as it can also be used for the preparation of benzoyl peroxide over. Benzoyl chloride, for analysis ACS, 98+% 500GR, Hydroxyl Group Labeling Reagents for HPLC, Enantiomer Excess & Absolute Conefiguration Determination, Exciton Chirality CD Method (for Hydroxyl Groups), Absolute Conefiguration Determination (Exciton Chirality CD Method), Absolute Configuration Determination (Exciton Chirality CD Method). RISK: Benzoyl chloride liquid is corrosive, and can cause redness, pain, and burns on contact with skin and eyes.
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