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About This Item
Linear Formula:
H2NC6H4C(O)NHNH2
CAS Number:
Molecular Weight:
151.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
95%
form
powder
mp
225-227 °C (lit.)
SMILES string
NNC(=O)c1ccc(N)cc1
InChI
1S/C7H9N3O/c8-6-3-1-5(2-4-6)7(11)10-9/h1-4H,8-9H2,(H,10,11)
InChI key
WPBZMCGPFHZRHJ-UHFFFAOYSA-N
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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Myeloperoxidase is a key regulator of oxidative stress mediated apoptosis in myeloid leukemic cells.
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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
A J Kettle et al.
The Biochemical journal, 321 ( Pt 2), 503-508 (1997-01-15)
Hypochlorous acid is the most powerful oxidant generated by neutrophils and is likely to contribute to the damage mediated by these inflammatory cells. The haem enzyme myeloperoxidase catalyses its production from hydrogen peroxide and chloride. 4-Aminobenzoic acid hydrazide (ABAH) is
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)
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