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
Beilstein:
878137
MDL number:
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
functional group
hydrazine
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:
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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
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 Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
57.2 °F
Flash Point(C)
14 °C
Regulatory Information
危险化学品
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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
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
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
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
Chirantan Kar et al.
Inorganic chemistry, 52(2), 743-752 (2013-01-11)
We have synthesized a new indole functionalized rhodamine derivative L(1) which specifically binds to Cu(2+) in the presence of large excess of other competing ions with visually observable changes in their electronic and fluorescence spectral behavior. These spectral changes are
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