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Benzohydroxamic acid

CAS No.
495-18-1
Chemical Name:
Benzohydroxamic acid
Synonyms
BHAM;NSC 3136;NSC 147248;benzohydroxamate;N-HYDROXYBENZAMIDE;Benzohydroxamsαure;n-hydroxy-benzamid;BENZOHYROXAMICACID;benzohydroxamicaci;BENZHYDROXAMIC ACID
CBNumber:
CB4764830
Molecular Formula:
C7H7NO2
Molecular Weight:
137.14
MDL Number:
MFCD00002109
MOL File:
495-18-1.mol
MSDS File:
SDS
Last updated:2023-11-13 16:15:56

Benzohydroxamic acid Properties

Melting point 126-130 °C(lit.)
Boiling point 251.96°C (rough estimate)
Density 1.2528 (rough estimate)
refractive index 1.5030 (estimate)
storage temp. 2-8°C
solubility Soluble in alcohol. Slightly soluble in ether. Insoluble in benzene.
form Solid
pka pK1: 8.89(0) (20°C)
color Rhombic tablets
Water Solubility 22 g/L (6 ºC)
BRN 1907585
Stability Moisture and Temperature Sensitive
InChIKey VDEUYMSGMPQMIK-UHFFFAOYSA-N
CAS DataBase Reference 495-18-1(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII K8YW73872D
NIST Chemistry Reference Benzamide, n-hydroxy-(495-18-1)
EPA Substance Registry System Benzohydroxamic acid (495-18-1)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS07,GHS08
Signal word  Warning
Hazard statements  H315-H319-H335-H341
Precautionary statements  P201-P261-P305+P351+P338-P405-P501a-P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
Hazard Codes  Xn
Risk Statements  68-40-20/21/22
Safety Statements  45-36/37-36-22
WGK Germany  3
RTECS  DF9650000
TSCA  Yes
HS Code  29280090
Toxicity LD orl-rat: >500 mg/kg NCNSA6 5,26,53
NFPA 704
1
2 0

Benzohydroxamic acid price More Price(31)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 412260 Benzhydroxamic acid 99% 495-18-1 5g $76.6 2024-03-01 Buy
TCI Chemical B0061 Benzohydroxamic Acid >98.0%(T) 495-18-1 5g $36 2024-03-01 Buy
TCI Chemical B0061 Benzohydroxamic Acid >98.0%(T) 495-18-1 25g $143 2024-03-01 Buy
Alfa Aesar A10509 Benzohydroxamic acid, 98% 495-18-1 10g $80.2 2024-03-01 Buy
Alfa Aesar A10509 Benzohydroxamic acid, 98% 495-18-1 25g $166 2024-03-01 Buy
Product number Packaging Price Buy
412260 5g $76.6 Buy
B0061 5g $36 Buy
B0061 25g $143 Buy
A10509 10g $80.2 Buy
A10509 25g $166 Buy

Benzohydroxamic acid Chemical Properties,Uses,Production

Chemical Properties

Crystalline Solid

Uses

Benzhydroxamic acid may be employed for the Pd-catalyzed synthesis of benzisoxazolones.

Uses

Benzhydroxamic acid is used as precursor in the synthesis of novel mono-anionic and di-anionic hydroxamato complexes by reacting with BiPh3 and Bi(O(t)Bu)3, which has anti-bacterial activity against helicobacter pylori. It is used in the photometric determination of trace amounts of vanadium in alloy steels by making mixed-ligand vanadium chelates with ammonium thiocyanate. It is also involved in the palladium catalyzed synthesis of benzisoxazolones.

Preparation

To a rapidly stirred suspension of 19.6 gm (0.35 mole) of powdered anhydrous potassium hydroxide in 120 ml of pyridine, maintained at 0-5°C, is a added a solution of 13.9 gm (0.2 mole) of hydroxylamine hy­drochloride in 100 ml of pyridine.
While maintaining the reaction temperature at 0-5°C, 15 gm (0.1 mole) of ethyl benzoate is added. Vigorous stirring is continued at room tempera­ture for 6 hr. Then the solids are filtered off. The solids are washed with cold water to remove inorganic coproducts. The remainder, recrystallized from aqueous ethanol, represents a 94% yield of potassium benzohy­droxamate.
This salt is triturated with cold 0.01 TV hydrochloric acid. From this mixture, by the usual procedures, 12.5 gm (91% overall) of benzohydrox­amic acid is isolated, m.p. 131°C (from aqueous alcohol).
Preparation of Benzohydroxamic Acid

Synthesis Reference(s)

Tetrahedron Letters, 33, p. 5055, 1992 DOI: 10.1016/S0040-4039(00)61187-5

General Description

Rhombic crystals or light beige solid.

Air & Water Reactions

Slightly soluble in water.

Reactivity Profile

Benzohydroxamic acid is an amide. Amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).

Health Hazard

ACUTE/CHRONIC HAZARDS: When heated to decomposition Benzohydroxamic acid emits toxic fumes of nitrogen oxides.

Fire Hazard

Flash point data for Benzohydroxamic acid are not available; however, Benzohydroxamic acid is probably combustible.

Safety Profile

Moderately toxic by ingestion.Mutation data reported. When heated to decomposition itemits toxic fumes of NOx.

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View Lastest Price from Benzohydroxamic acid manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Benzohydroxamic acid pictures 2023-11-13 Benzohydroxamic acid
495-18-1
US $0.00 / KG 1KG 99% 50000KG/month Hebei Mojin Biotechnology Co., Ltd
Benzohydroxamic acid pictures 2023-09-13 Benzohydroxamic acid
495-18-1
US $0.00 / kg 1kg 0.99 20tons Hebei Yanxi Chemical Co., Ltd.
Benzohydroxamic acid pictures 2023-09-06 Benzohydroxamic acid
495-18-1
US $0.00-0.00 / KG 1KG 99% 500000kg Hebei Guanlang Biotechnology Co., Ltd.
BENZHYDROXAMIC ACID BENZOHYDROXAMIC ACID N-HYDROXYBENZAMIDE N-BENZOYLHYDROXYLAMINE Benzamide,N-hydroxy- benzohydroxamate n-hydroxy-benzamid Phenylhydroxamic acid phenylhydroxamicacid Benzohydroxamsαure Benzoylhydroxamic acid benzoylhydroxamicacid Hydroxylamine, N-benzoyl- BenzohydroxamicAcid,>98% Benzamide, N-hydroxy- (9CI) Benzohydroxamicacid,99% BENZOHYROXAMICACID N-Benzoylhydroxylamine,Benzhydroxamicacid BENZHYDROXAMIC ACID extrapure BHAM Benzeneformhydroxamic acid Benzhydroxamic acid,N-Hydroxybenzamide NSC 147248 NSC 3136 Benzhydroxamic acid 99% Benzohydroxamic acid for synthesis BENZOYL HYDROXIMIC ACID Benzohydroxamic Acid > benzohydroxamicaci Benzohydroxamic Acid extrapure, 99% enzohydroxamic acid Benzohydroxamic acid (6CI, 8CI) BENZHYDROXAMIC ACID(BHA) 495-18-1 C7H7NO2 Hydroxylamines (N-Substituted) Hydroxylamines Organic Building Blocks Nitrogen Compounds C7 Carbonyl Compounds Carboxylic Acids Building Blocks Aromatics AMIDE Hydroxylamines Hydroxylamines (N-Substituted) Inhibitors