A41909
4-Aminobenzoic hydrazide
95%
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About This Item
Linear Formula:
H2NC6H4C(O)NHNH2
CAS Number:
Molecular Weight:
151.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
226-324-4
MDL number:
Assay:
95%
Form:
powder
InChI key
WPBZMCGPFHZRHJ-UHFFFAOYSA-N
InChI
1S/C7H9N3O/c8-6-3-1-5(2-4-6)7(11)10-9/h1-4H,8-9H2,(H,10,11)
SMILES string
NNC(=O)c1ccc(N)cc1
assay
95%
form
powder
mp
225-227 °C (lit.)
Quality Level
Related Categories
Application
4-Aminobenzoic hydrazide can be used as a reactant to synthesize:
- Acylhydrazone Schiff base ligand by condensation reaction with 2-acetylpyridine.
- Oligomeric transition metal complexes applicable in the fabrication of organic-inorganic hybrid devices with efficient electrical and photoelectrical properties.
- Oxovanadium(IV)-hydrazide complex as a potential radical scavenger.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
监管及禁止进口产品
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Electrical and photoelectrical behaviour of heterojunctions based on novel oligomeric metal complexes
Atlan M, et al.
Applied Organometallic Chemistry, 29(12) (2015)
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Clinical cancer research : an official journal of the American Association for Cancer Research, 13(18 Pt 1), 5436-5445 (2007-09-19)
We reported previously that reactive oxygen species (ROS) are key mediators of apoptosis induced by a polyphenol, (-)-epigallocatechin-3-gallate (EGCG), in myeloid leukemic cells. This study aimed to further examine the mechanism of ROS-mediated apoptosis induced by EGCG and its relationship
U Burner et al.
The Journal of biological chemistry, 274(14), 9494-9502 (1999-03-27)
Myeloperoxidase is the most abundant protein in neutrophils and catalyzes the production of hypochlorous acid. This potent oxidant plays a central role in microbial killing and inflammatory tissue damage. 4-Aminobenzoic acid hydrazide (ABAH) is a mechanism-based inhibitor of myeloperoxidase that
Enzyme inhibition, radical scavenging, and spectroscopic studies of vanadium (IV)-hydrazide complexes
Ashiq U, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry, 24(6), 1336-1343 (2009)
Preparation of porous resin with Schiff base chelating groups for removal of heavy metal ions from aqueous solutions
Ceglowski M and Schroeder G
Chemical Engineering Journal, 263 (2015)
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