B13071
Benzhydrazide
98%
Synonym(s):
Benzoic acid hydrazide, Benzoylhydrazine
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About This Item
Linear Formula:
C6H5CONHNH2
CAS Number:
Molecular Weight:
136.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-363-9
Beilstein/REAXYS Number:
471797
MDL number:
Assay:
98%
Form:
powder
Product Name
Benzhydrazide, 98%
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
SMILES string
NNC(=O)c1ccccc1
assay
98%
form
powder
mp
112-114 °C (lit.)
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Related Categories
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Skin Irrit. 2
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
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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
Sylvain Broussy et al.
The Journal of organic chemistry, 70(25), 10502-10510 (2005-12-06)
[reaction: see text] An isoniazid-NAD adduct has been recently proposed as the ultimate metabolite responsible for the antituberculous activity of isoniazid (INH). Its structure results from binding of the isonicotinoyl radical at C4 position of the nicotinamide ring of NAD
Tetsuya Toya et al.
Bioorganic & medicinal chemistry, 10(4), 953-961 (2002-02-12)
We have investigated the biologically active conformation of the non-steroidal ecdysone agonist, 1-tert-butyl-1,2-dibenzoylhydrazine (RH-5849) by means of design, synthesis and conformational analysis of cyclic derivatives of RH-5849. Among the synthesized compounds, a 6-membered cyclic hydrazine bearing two benzoyl groups (5)
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
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