901596
Hydrazine solution
1.0 M in ethanol
Sinónimos:
Hydrazine, Nitrogen hydride
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About This Item
Fórmula lineal:
NH2NH2
Número de CAS:
Peso molecular:
32.05
Beilstein:
878137
Número MDL:
Código UNSPSC:
12352100
NACRES:
NA.22
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Formulario
liquid
concentración
1.0 M in ethanol
índice de refracción
n/D 1.3666
densidad
0.7934 g/mL
grupo funcional
hydrazine
cadena SMILES
NN
InChI
1S/H4N2/c1-2/h1-2H2
Clave InChI
OAKJQQAXSVQMHS-UHFFFAOYSA-N
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Descripción general
Hydrazine promotes the cation exchange reaction for fast doping Cu ions into ZnSe nanocrystals.
Aplicación
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.
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Referencia del producto
Descripción
Precios
Palabra de señalización
Danger
Frases de peligro
Consejos de prudencia
Clasificaciones de peligro
Acute Tox. 4 Inhalation - Aquatic Chronic 2 - Carc. 1B - Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - Skin Sens. 1
Código de clase de almacenamiento
3 - Flammable liquids
Clase de riesgo para el agua (WGK)
WGK 3
Punto de inflamabilidad (°F)
57.2 °F
Punto de inflamabilidad (°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
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
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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