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Benzoyl chloride

CAS No.98-88-4
Chemical Name:Benzoyl chloride
Synonyms:Basic Red 1;BENZOXALONE;Benzoylchlorid;BENZOYL CHLORIDE;BenzoylChlorideGr;chloruredebenzoyle;-Chlorobenzaldehyde;BENZOIC ACID CHLORIDE;BENZOYL CHLORIDE, ACS;LABOTEST-BB LTBB000456
CBNumber:CB8854753
Molecular Formula:C7H5ClO
Formula Weight:140.57
MOL File:98-88-4.mol
Benzoyl chloride Property
mp : -1 °C
bp : 198 °C(lit.)
density : 1.211 g/mL at 25 °C(lit.)
vapor density : 4.88 (vs air)
vapor pressure : 1 mm Hg ( 32 °C)
refractive index : n20/D 1.553(lit.)
Fp : 156 °F
storage temp. : Store at 0-5°C
Water Solubility : reacts
FreezingPoint : -1℃
Sensitive : Moisture Sensitive
Merck : 14,1112
Stability:: Stable. Combustible. Incompatible with strong oxidizing agents, water, alcohols, strong bases. Reacts violently with DMSO and vigorously with alkalies.
CAS DataBase Reference: 98-88-4(CAS DataBase Reference)
NIST Chemistry Reference: Benzoyl chloride(98-88-4)
EPA Substance Registry System: Benzoyl chloride(98-88-4)
Safety
Hazard Codes : C
Risk Statements : 34-43-20/21/22
Safety Statements : 26-45-36/37/39
RIDADR : UN 1736 8/PG 2
WGK Germany : 1
RTECS : DM6600000
Hazard Note : Corrosive
HazardClass : 8
PackingGroup : II
HS Code : 29310095
Hazardous Substances Data: 98-88-4(Hazardous Substances Data)

Benzoyl chloride Chemical Properties,Usage,Production

Chemical Properties
Colorless liquid
Usage
Benzoyl Chloride is used in the manufacturing of dye intermediates.
General Description
A colorless fuming liquid with a pungent odor. Flash point 162°F. Lachrymator, irritating to skin and eyes. Corrosive to metals and tissue. Density 10.2 lb / gal. Used in medicine and in the manufacture of other chemicals.
Reactivity Profile
Benzoyl chloride reacts violently with protic solvents such as alcohols, with amines and amides (for example dimethylformamide [Bretherick 1979 p. 6] ) and with inorganic bases. Causes the violent decomposition of dimethyl sulfoxide [Chem. Eng. News 35(9): 87 1957]. 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]. Friedel-Crafts acylation of naphthalene using Benzoyl chloride, catalyzed by AlCl3, must be conducted above the melting point of the mixture, or the reaction may be violent [Clar, E. et al., Tetrahedron, 1974, 30, 3296].
Health Hazard
INHALATION: may irritate eyes, nose and throat. INGESTION: causes acute discomfort. SKIN: causes irritation and burning.
Benzoyl chloride Preparation Products And Raw materials
Raw materials
Toluene Chlorine Benzotrichloride Phosphorus trichloride PHOSGENE Benzoic acid
Preparation Products
3-oxo-3-phenyl-propanamide N,N-Dimethylpiperidin-4-amine APLPHA-BROMO-M-BENZOYLOXYACETOPHENONE 2-(N,N-DIETHYLAMINOCARBONYL)PHENYLBORONIC ACID 2-Methyoxy-3-methyl-2-phenyl-4H-benzo-g-pyranone (+)-Dibenzoyl-D-tartaric acid DIBENZOYL THIAMINE PHENOXYACETIC ACID Benzoyl cyanide 2,5-DICHLOROBENZOYL CHLORIDE 7-HYDROXY-3-METHYLFLAVONE 1-BENZOYLPIPERIDINE Proglumide 4-Chlorobenzophenone Histamine (3,4-Diaminophenyl)phenylmethanone Sucrose benzoate 1,3-DIBENZOYLOXYBENZENE QUINOLINE-2-CARBONITRILE 1-NAPHTHYL PHENYL KETONE tert-Butyl peroxybenzoate 3,4-Dichlorobenzophenone Fast Blue BB dihydroxyethyl p-octadecyl phenylsulfonyl amino propyl ammoium propylsulfonate 3-Chlorobenzoyl chloride 2-Amino-5-nitrobenzophenone Chrysin N,N'-DIBENZOYLHYDRAZINE N-Phenylbenzohydroxamic acid N,N-Dimethylbenzamide Phenyl benzoate Nitrazepam dibenzoyl disulphide 1-(PHENYLSULFONYL)-1H-INDOLE-2-CARBALDEHYDE Oxybenzone 4-BROMOPHENYLTHIOUREA 1-BENZOYLPIPERAZINE HYROCHLORIDE 97 2-AMINO-1-PHENYLETHANOL Benzoylferrocene 4-Chloro-2-methylaniline
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98-88-4(Benzoyl chloride)Related Search:
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alpha-chloro-benzaldehyd Benzaldehyde, alpha-chloro- -Chlorobenzaldehyde chloruredebenzoyle HPLC Labeling Reagents Hydroxyl Group Labeling Reagents for HPLC Amino Group Labeling Reagents for HPLC Reagents for Oligosaccharide Synthesis UV Detection (HPLC Labeling Reagents) Enantiomer Excess & Absolute Conefiguration Determination Exciton Chirality CD Method (for Hydroxyl Groups) Absolute Conefiguration Determination (Exciton Chirality CD Method) LABOTEST-BB LTBB000456 Benzenecarbonyl chloride BENZOIC ACID CHLORIDE BENZOYL CHLORIDE 98-88-4 alpha-Chlorobenzaldehyde Acid Halides Building Blocks Carbonyl Compounds Organic Building Blocks ACID CHLORIDE BENZOYL CHLORIDE, REAGENTPLUS, >=99% BENZOYL CHLORIDE REAGENTPLUSTM >=99% BENZOYL CHLORIDE, REAGENTPLUS, 99% BENZOYL CHLORIDE, 99%, A.C.S. REAGENT BENZOYL CHLORIDE REAGENTPLUS(TM) 99% BENZOYL CHLORIDE, ACS BenzoylChlorideGr Benzoyl chloride, 99+% Benzoyl chloride, for analysis ACS, 98+% Benzoyl chloride, pure, 99% BENZOYL CHLORIDE REAGENT (ACS) C6H5COCl Pharmaceutical Intermediates Benzoylchlorid Organics Basic Red 1 BENZOXALONE Absolute Configuration Determination (Exciton Chirality CD Method) Amino Group Labeling Reagents for HPLC Analytical Chemistry Biochemistry Enantiomer Excess & Absolute Configuration Determination Exciton Chirality CD Method (for Hydroxyl Groups) HPLC Labeling Reagents Hydroxyl Group Labeling Reagents for HPLC Nucleosides, Nucleotides & Related Reagents Protecting Agents for Hydroxyl and Amino Groups Protecting Agents, Phosphorylating Agents & Condensing Agents Reagents for Oligosaccharide Synthesis UV Detection (HPLC Labeling Reagents) A-B, Puriss p.a. ACSOrganic Building Blocks Acid HalidesDerivatization Reagents Analytical Reagents for General Use Carbonyl Compounds Derivatization Reagents HPLC
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