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Merck

901596

Hydrazine solution

1.0 M in ethanol

Synonym(s):

Hydrazine, Nitrogen hydride

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About This Item

Linear Formula:
NH2NH2
CAS Number:
Molecular Weight:
32.05
NACRES:
NA.22
UNSPSC Code:
12352100
Beilstein/REAXYS Number:
878137
MDL number:
Form:
liquid
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form

liquid

concentration

1.0 M in ethanol

refractive index

n/D 1.3666

density

0.7934 g/mL

functional group

hydrazine

SMILES string

NN

InChI

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

InChI key

OAKJQQAXSVQMHS-UHFFFAOYSA-N

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.


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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

WGK 3

flash_point_f

57.2 °F

flash_point_c

14 °C


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

302-01-2

CAS No.

302-01-2

CAS No.


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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
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