ChemicalBook Product Catalog Organic Chemistry Hydrazine or hydroxylamine derivatives 4-Hydrazinobenzoic acid hydrochloride

4-Hydrazinobenzoic acid hydrochloride

4-Hydrazinobenzoic acid hydrochloride Basic information
Product Name:4-Hydrazinobenzoic acid hydrochloride
Synonyms:LABOTEST-BB LT01596126;BIO-FARMA BF001082;P-CARBOXYPHENYL HYDRAZINE HCL;P HYDRAZINOBENZOIC ACID HYDROCHLORIDE;4-CARBOXYPHENYLHYDRAZINE HYDROCHLORIDE;4-HYDRAZINOBENZOIC ACID HCL;4-HYDRAZINOBENZOIC ACID HYDROCHLORIDE;4-hydrazino-benzoicacimonohydrochloride
CAS:24589-77-3
MF:C7H9ClN2O2
MW:188.61
EINECS:246-330-0
Product Categories:FINE Chemical & INTERMEDIATES;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Phenylhydrazine;API intermediates;Hydrazines;Nitrogen Compounds;Organic Building Blocks
Mol File:24589-77-3.mol
4-Hydrazinobenzoic acid hydrochloride Structure
4-Hydrazinobenzoic acid hydrochloride Chemical Properties
Melting point 253 °C (dec.)(lit.)
storage temp. 2-8°C
solubility DMSO (Slightly), Methanol (Sparingly)
form Solid
color White to Off-White
Water Solubility Soluble in water.
InChIKeyXHLQMKQBCHYRLC-UHFFFAOYSA-N
CAS DataBase Reference24589-77-3(CAS DataBase Reference)
EPA Substance Registry SystemBenzoic acid, 4-hydrazino-, monohydrochloride (24589-77-3)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
RTECS DH1700000
TSCA Yes
HS Code 2928009090
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
4-Hydrazinobenzoic acid hydrochloride Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powder     
Uses4-Hydrazinobenzoic acid hydrochloride is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields. It may be used for the preparation of 4-(3-(2-(tert-butoxycarbonylamino)ethyl)-5-hydroxy-1H-pyrazol-1-yl)benzoic acid.
General Description4-Hydrazinobenzoic acid (p-Hydrazinobenzoic acid, HBA) has been reported as an ingredient of the cultivated mushroom Agaricus bisporus. It is carcinogenic to rodents. Mechanism of DNA damage by 4-hydrazinobenzoic acid has been studied by using 32P-labeled DNA fragments obtained from the human p53 and p16 tumor suppressor genes. It may be used for the preparation of 4-(3-(2-(tert-butoxycarbonylamino)ethyl)-5-hydroxy-1H-pyrazol-1-yl)benzoic acid.
4-Hydrazinobenzoic acid hydrochloride Preparation Products And Raw materials
4-Hydrazinylbenzoic acid Phenylhydrazine hydrochloride Carboxy styrene-butadiene latex 2-Ethylphenylhydrazine hydrochloride ETHYL 4-[5-CHLORO-4-MORPHOLINO-6-OXOPYRIDAZIN-1(6H)-YL]BENZOATE ETHYL 4-[5-CHLORO-4-(DIETHYLAMINO)-6-OXOPYRIDAZIN-1(6H)-YL]BENZOATE Topotecan hydrochloride ETHYL 4-[5-CHLORO-4-(2,6-DIMETHYLMORPHOLINO)-6-OXOPYRIDAZIN-1(6H)-YL]BENZOATE ETHYL 4-[(2E)-2-(1-CHLORO-2-OXOPROPYLIDENE)HYDRAZINO]BENZOATE 4-Hydrazinobenzoic acid hydrochloride 4-(N'-(1-[4-(4-CHLORO-PHENYL)-THIAZOL-2-YL]-3-METHYL-5-OXO-1,5-DIHYDRO-PYRAZOL-4-YLIDENE)-HYDRAZINO)-BENZOIC ACID ETHYL 4-[(2E)-2-(1-CHLORO-2-ETHOXY-2-OXOETHYLIDENE)HYDRAZINO]BENZOATE 1-Acetyl-2-phenylhydrazine RARECHEM AL BO 2178 4-Formylbenzoic acid 2,3-DICHLORO-4-(2-[4-(ETHOXYCARBONYL)PHENYL]HYDRAZONO)BUT-2-ENOIC ACID 2-CHLORO-4-HYDRAZINO-BENZOIC ACID p-Carboxylphenylacetic acid
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