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Sigma-Aldrich

Hydrazine dihydrochloride

≥98%

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About This Item

Linear Formula:
NH2NH2 · 2HCl
CAS Number:
5341-61-7
Molecular Weight:
104.97
EC Number:
226-283-2
MDL number:
MFCD00064543
UNSPSC Code:
12352300
PubChem Substance ID:
24852941
NACRES:
NA.21

Quality Level

100

assay

≥98%

form

powder, crystals or chunks
solid

mp

200 °C (dec.) (lit.)

density

1.42 g/mL at 25 °C (lit.)

SMILES string

Cl[H].Cl[H].NN

InChI

1S/2ClH.H4N2/c;;1-2/h2*1H;1-2H2

InChI key

LIAWOTKNAVAKCX-UHFFFAOYSA-N

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General description

Hydrazine dihydrochloride can be used as a reducing agent in the conversion of carbonyls to methylene compounds and α, β-epoxyketones to allylic alcohols. It can also reduce alkenes, alkynes, and nitro groups. In addition, it is used to synthesize hydrazides and dinitrogen-containing heterocycles.

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Description
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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

wgk_germany

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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Rapid synthesis of 2, 5-disubstituted 1, 3, 4-oxadiazoles under microwave irradiation.
Bentiss F, et al.
Synthetic Communications, 31(6), 935-938 (2001)
A silver colloid produced by reduction with hydrazine as support for highly sensitive surface-enhanced Raman spectroscopy
Nickel U, et al.
Langmuir, 16(23), 9087-9091 (2000)
Spectrophotometric method for determination of hydrazine.
Watt GW and Chrisp JD.
Analytical Chemistry, 24(12), 2006-2008 (1952)
Accelerated synthesis of 3, 5-disubstituted 4-amino-1, 2, 4-triazoles under microwave irradiation.
Bentiss F, et al.
Tetrahedron Letters, 41(10), 1539-1541 (2000)
Ranendu Sekhar Das et al.
Dalton transactions (Cambridge, England : 2003), 42(11), 4068-4080 (2013-01-24)
PVP capped platinum nano particles (PNP) of 5 nm diameter were prepared and characterized as homogeneous and of spherical nature. At physiological pH range (6.0-8.0), these PNP catalyze the deoxygenation of phenoxazine group containing resazurin (1) by hydrazine. The observed
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