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Merck

442232-U

Supelco

1,2-Diphenylhydrazin

analytical standard, ampule of 100 mg

Synonym(e):

Hydrazobenzol, N,N′-Diphenylhydrazin, N,N′-Bianilin, NSC 3510

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About This Item

Lineare Formel:
C6H5NHNHC6H5
CAS-Nummer:
Molekulargewicht:
184.24
Beilstein:
639793
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
77101502
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

analytical standard

Analysenzertifikat (CofA)

current certificate can be downloaded

Verpackung

ampule of 100 mg

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

mp (Schmelzpunkt)

123-126 °C (lit.)

Anwendung(en)

cleaning products
cosmetics
environmental
food and beverages
personal care

Format

neat

Lagertemp.

2-30°C

SMILES String

N(Nc1ccccc1)c2ccccc2

InChI

1S/C12H12N2/c1-3-7-11(8-4-1)13-14-12-9-5-2-6-10-12/h1-10,13-14H

InChIKey

YBQZXXMEJHZYMB-UHFFFAOYSA-N

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Allgemeine Beschreibung

1,2-Diphenylhydrazine is mainly used in the manufacture of fabrics and medicines. Its other applications include, but not limited to: a precursor of benzidine, an antisludging additive for motor oil, a constituent in photochromic resins as well as in polymers, and syntheses of hydrogen peroxide (H2O2) and several dyestuffs.

Anwendung

1,2-Diphenylhydrazine may be used as an analytical standard for the determination of the analyte in landfill leachate, pharmaceutical process stream, and aqueous solutions by high-performance liquid chromatography (HPLC) and gas chromatography (GC) based analytical techniques.
Reactant involved in:
  • Insertion reactions with organometallic tantalum complexes
  • Reduction reactions catalyzed by titanium(III) trichloride yielding amines
  • Studying the mechanism of hydrazobenzene rearrangement
  • Reaction with N-heterocyclic stable silylene
  • Synthesis of dimanganese amide hydrazide cluster complexes
  • Iron-mediated hydrazine reductions yielding iron arylimide cubanes
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B

Lagerklassenschlüssel

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves, type P2 (EN 143) respirator cartridges


Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

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In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Joonas Jernberg et al.
Talanta, 103, 384-391 (2012-12-04)
Nontarget analysis means that a sample is analysed without preselection of the studied analytes. While target analysis attempts to determine whether certain selected compounds are present in the sample, nontarget analysis is performed to explore what unknown compounds can be
Darol E Dodd et al.
International journal of toxicology, 31(6), 564-571 (2012-11-09)
Male F344 rats were exposed to hydrazobenzene (HZB) by dietary feed at concentrations of 0, 5, 20, 80, 200, or 300 ppm for 5 days, 2 weeks, 4 weeks, or 13 weeks duration. End points evaluated included clinical observations, body
Hydrazobenzene.
Report on carcinogens : carcinogen profiles, 10, 139-140 (2004-08-26)
H Fabre et al.
Journal of pharmaceutical sciences, 73(12), 1706-1709 (1984-12-01)
A high-performance liquid chromatographic method was developed for the simultaneous determination of azobenzene, hydrazobenzene, and four other decomposition products in phenylbutazone injectable formulations. Separation was achieved on a C18 column, with 0.1 M Tris-citrate buffer (pH 5.25) and acetonitrile (52:48)
Jenny V Lockard et al.
The journal of physical chemistry. A, 109(6), 1205-1215 (2006-07-13)
A quantitative model of mixed-valence excited-state spectroscopy is developed and applied to 2,3-diphenyl-2,3-diazabicyclo[2.2.2]octane. The lowest-energy excited state of this molecule arises from a transition from the ground state, where the charge is located on the hydrazine bridge, to an excited

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