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B13071

Sigma-Aldrich

Benzhydrazide

98%

Synonym(s):

Benzoic acid hydrazide, Benzoylhydrazine

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About This Item

Linear Formula:
C6H5CONHNH2
CAS Number:
613-94-5
Molecular Weight:
136.15
Beilstein:
471797
EC Number:
210-363-9
MDL number:
MFCD00007596
UNSPSC Code:
12352100
PubChem Substance ID:
24891580
NACRES:
NA.22

Assay

98%

form

powder

mp

112-114 °C (lit.)

SMILES string

NNC(=O)c1ccccc1

InChI

1S/C7H8N2O/c8-9-7(10)6-4-2-1-3-5-6/h1-5H,8H2,(H,9,10)

InChI key

WARCRYXKINZHGQ-UHFFFAOYSA-N

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Pictograms

Health hazardExclamation mark
GHS08,GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H351

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Skin Irrit. 2

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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E Agostinelli et al.
The Biochemical journal, 324 ( Pt 2), 497-501 (1997-06-01)
A novel copper-depleted bovine serum amine oxidase (BSAO), in which about half the molecules contained the organic cofactor in the oxidized form, was prepared by adding a reductant in anaerobic conditions to the cyanide-reacted protein. The CuI-semiquinone formed in these
M Kobayashi et al.
Biochemical and biophysical research communications, 256(2), 415-418 (1999-03-18)
The amidase from Rhodococcus rhodochrous J1, which hydrolyses amide to acid and ammonia, was found to catalyze the synthesis of hydrazide using hydrazine as a substrate. This is the first report on the hydrazide synthesis through enzymatic reactions. The enzyme
Venkataswamy Sorna et al.
Journal of medicinal chemistry, 56(23), 9496-9508 (2013-11-19)
Lysine specific demethylase 1 (LSD1) plays an important role in regulating histone lysine methylation at residues K4 and K9 on histone H3 and is an attractive therapeutic target in multiple malignancies. Here we report a structure-based virtual screen of a
Susan M Aitken et al.
The Biochemical journal, 375(Pt 3), 613-621 (2003-07-19)
Many compounds are oxidized by haem enzymes, such as peroxidases and cytochromes P450, to highly reactive intermediates that function as enzyme inactivators. To evaluate the potential of arylhydrazides as selective metabolically activated peroxidase inhibitors, the mechanism of HRPC (horseradish peroxidase
V Arjunan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(3), 486-496 (2011-05-03)
A systematic vibrational spectroscopic assignment and analysis of benzohydrazide (BH) has been carried out by using FTIR and FT-Raman spectral data. The vibrational analysis were aided by electronic structure calculations--ab initio (RHF) and hybrid density functional methods (B3LYP and B3PW91)
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