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901596

Sigma-Aldrich

Hydrazine solution

1.0 M in ethanol

Sinónimos:

Hydrazine, Nitrogen hydride

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About This Item

Fórmula lineal:
NH2NH2
Número de CAS:
302-01-2
Peso molecular:
32.05
Beilstein/REAXYS Number:
878137
MDL number:
MFCD00011417
UNSPSC Code:
12352100
NACRES:
NA.22

form

liquid

concentration

1.0 M in ethanol

refractive index

n/D 1.3666

density

0.7934 g/mL

SMILES string

NN

InChI

1S/H4N2/c1-2/h1-2H2

InChI key

OAKJQQAXSVQMHS-UHFFFAOYSA-N

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General description

Hydrazine promotes the cation exchange reaction for fast doping Cu ions into ZnSe nanocrystals.

Application

Valuable building block provided in ethanol for convenient handling.
Hydrazine solution may be employed for the following studies:
  • As reducing agent for the reduction of the first row (3d) transition metal complexes in aqueous solution.
  • Preparation of nanoscale reduced metal oxides such as VO2(B), Cr2O3.
  • As fuel for the direct hydrazine fuel cell (DHFC).
  • As reducing agent for the synthesis of metallic monodisperse copper nanoparticles.

related product

Referencia del producto
Descripción
Precios

H4766

Hydrazine hemisulfate salt, ≥98%

53900

Hydrazine sulfate salt, puriss. p.a., ACS reagent, ≥99.0%

216046

Hydrazine sulfate salt, ACS reagent, ≥99.0%

259748

Hydrazine acetate, 97%

309400

Hydrazine solution, 35 wt. % in H2O

216194

Hydrazine monohydrochloride, 97%

216208

Hydrazine dihydrochloride, ≥98%

225819

Hydrazine hydrate, reagent grade, N2H4 50-60 %

215155

Hydrazine, anhydrous, 98%

207942

Hydrazine monohydrate, N2H4 64-65 %, reagent grade, ≥97%

394440

Hydrazine monohydrobromide, ≥98%

433632

Hydrazine solution, 1.0 M in THF

751855

Hydrazine solution, 1 M in acetonitrile

53847

Hydrazine hydrate solution, puriss. p.a., 24-26% in H2O (RT)

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Aquatic Chronic 2 - Carc. 1B - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - Skin Sens. 1

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

57.2 °F

flash_point_c

14 °C

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M Vogel et al.
Fresenius' journal of analytical chemistry, 366(8), 781-791 (2001-03-03)
Hydrazine reagents are a well-known group of derivatizing agents for the determination of aldehydes and ketones in liquid and gaseous samples. Within this article, the most important hydrazine reagents are critically summarized, and their major applications in different fields, including
Nilay Hazari
Chemical Society reviews, 39(11), 4044-4056 (2010-06-24)
One of the most challenging problems in small molecule activation is the development of a homogeneous catalyst for converting dinitrogen into ammonia at ambient temperatures and atmospheric pressure. A catalytic cycle based on molybdenum that converts dinitrogen into ammonia has
Min Yuan et al.
Dalton transactions (Cambridge, England : 2003), (31)(31), 6078-6088 (2010-05-08)
A combination of unique solvent properties of hydrazine enables the direct dissolution of a range of metal chalcogenides at ambient temperature, rendering this an extraordinarily simple and soft synthetic approach to prepare new metal chalcogenide-based materials. The extended metal chalcogenide
D P Elder et al.
Journal of pharmaceutical and biomedical analysis, 54(5), 900-910 (2010-12-15)
This is the latest of a series of reviews focused on the analysis of genotoxic impurities. This review summarises the analytical approaches reported in the literature relating to hydrazine, hydrazines, hydrazides and hydrazones. It is intended to provide guidance for
Yinhu Wang et al.
Biosensors & bioelectronics, 43, 180-185 (2013-01-12)
We report a novel hydrogen peroxide (H2O2) and hydrazine sensor based on low-cost poly(vinylpyrrolidone)-protected silver nanocubes (PVP-AgNCs). The monodisperse silver nanocubes were prepared by adding a trace amount of sodium sulfide in the conventional polyol synthesis for fast reduction of
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