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Merck

216194

Hydrazine monohydrochloride

97%

동의어(들):

Hydrazinium chloride, Hydrazinium monochloride

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제품정보 (DICE 배송 시 비용 별도)

Linear Formula:
NH2NH2 · HCl
CAS 번호:
Molecular Weight:
68.51
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
220-154-4
MDL number:
Assay:
97%
Form:
solid
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Quality Level

assay

97%

form

solid

mp

89 °C (lit.)

functional group

hydrazine

SMILES string

Cl[H].NN

InChI

1S/ClH.H4N2/c;1-2/h1H;1-2H2

InChI key

BIVUUOPIAYRCAP-UHFFFAOYSA-N

General description

Hydrazine monohydrochloride is commonly used as a reagent in the synthesis of pyrazoles.

Application

Hydrazine monohydrochloride has been used:
  • as catalyst in the synthesis of titanium oxide polymers via catalytic sol-gel process
  • in fabrication of amorphous titanium dioxide (TiO2) thin films exhibiting high refractive indices and high transparency
  • in preparation of ethyl 3-ethoxy-1H-pyrazole-4-carboxylate


signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 1B - Skin Sens. 1

저장 등급

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges



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문서 라이브러리 방문



Wataru Shimizu et al.
Langmuir : the ACS journal of surfaces and colloids, 28(33), 12245-12255 (2012-07-24)
Amorphous titanium dioxide (TiO(2)) thin films exhibiting high refractive indices (n ≈ 2.1) and high transparency were fabricated by spin-coating titanium oxide liquid precursors having a weakly branched polymeric structure. The precursor solution was prepared from titanium tetra-n-butoxide (TTBO) via
Tomáš Taubner et al.
International journal of biological macromolecules, 103, 202-207 (2017-05-21)
Alginic acid is a suitable material for modification to prepare new derivatives because of presence of its carboxyl groups. The high content of carboxyl groups over the entire length of its chain renders it an easily modifiable material with a
Sandrine Guillou et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 16(15), 4669-4677 (2010-03-25)
Our program, which has focused on the preparation of new pyrazole derivatives, has led us to report here an original and simplified preparation of ethyl 3-ethoxy-1H-pyrazole-4-carboxylate. This is based on the reaction of hydrazine monohydrochloride and diethyl 2-(ethoxymethylene)malonate. Further transformations