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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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Sigma-Aldrich

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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
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
Liping Bai et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 214, 436-444 (2019-02-27)
A simple water-soluble polymer PEGBHB based on polyethylene glycol bearing a Schiff base derivative moiety was successfully designed and synthesized. PEGBHB showed high selectivity and sensitivity towards Al3+ as a turn-on fluorescent chemosensor without influence by other competitive metal ions
Daniel E Carvajal-Hausdorf et al.
Journal for immunotherapy of cancer, 5(1), 81-81 (2017-10-19)
Immunostimulatory therapies targeting immune-suppressive pathways produce durable responses in advanced solid tumors. Indoleamine 2,3-dioxygenase (IDO) is the rate-limiting oxidoreductase that catalyzes the degradation of tryptophan to kynurenine. IDO induces immune tolerance by downregulating CD8+ and effector CD4+ T cell responses.
S Srinivasan et al.
Journal of inorganic biochemistry, 99(3), 876-882 (2005-02-15)
Cobalt(III) complexes of the type [Co(N-N)2L](ClO4)2.H2O [where L=anionic form of para-substituted benzaldehyde-benzoylhydrazone (BHBX-); X=H, Me, OMe, OH, Cl or NO2; N-N=2,2'-bipyridine (bpy) or 1,10-phenanthroline (phen)] have been synthesized and characterized through UV-Vis, IR, NMR and electrochemical studies. The IR spectral
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