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H4766

Sigma-Aldrich

Hydrazine hemisulfate salt

≥98%

Synonym(s):

Dihydrazine sulfate, Dihydrazinium sulfate

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About This Item

Linear Formula:
H2NNH2 · 1/2H2SO4
CAS Number:
13464-80-7
Molecular Weight:
81.08
EC Number:
236-688-6
MDL number:
MFCD00067695
UNSPSC Code:
12352100
PubChem Substance ID:
57654256
NACRES:
NA.22

Assay

≥98%

SMILES string

NN.NN.OS(O)(=O)=O

InChI

1S/2H4N2.H2O4S/c2*1-2;1-5(2,3)4/h2*1-2H2;(H2,1,2,3,4)

InChI key

DBLJAFVPFHRQSP-UHFFFAOYSA-N

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Application

  • Hydrogen Generation from Hydrolytic Dehydrogenation of Hydrazine Borane: Discusses the generation of hydrogen from hydrazine hemisulfate and its potential applications in hydrogen energy sources (Tunç et al., 2015).

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Signal Word

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

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Timothy M Alligrant et al.
Lab on a chip, 13(3), 349-354 (2012-12-06)
We report on real-time electrochemical detection of individual DNA hybridization events at an electrode surface. The experiment is carried out in a microelectrochemical device configured with a working electrode modified with single-stranded DNA probe molecules. When a complementary DNA strand
Hatem A Abdel-Aziz et al.
Molecules (Basel, Switzerland), 18(2), 2084-2095 (2013-02-08)
Although salicylaldehyde azine (3) was reported in 1985 as the single product of the reaction of ethyl 2-oxo-2H-chromene-3-carboxylate (1) with hydrazine hydrate, we identified another main reaction product, besides 3, which was identified as malono-hydrazide (4). In the last
Paul D Rainville et al.
Bioanalysis, 4(23), 2833-2842 (2012-12-12)
Accurate mass based LC-MS combined with statistical analysis is established as a core analytical technology for metabonomic studies. This is primarily due to the specificity, sensitivity and structural elucidation capabilities of the technology. The vast majority of these studies are
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
Muhammad Baseer et al.
Pakistan journal of pharmaceutical sciences, 26(1), 67-73 (2012-12-25)
Fourteen new N-acetylated and non-acetylated pyrazoline derivatives were synthesized by reacting chalcones with hydrazine in the presence of absolute ethanol however reaction was carried out in the presence of glacial acetic acid to afford N-acetylated pyrazolines. The chemical structures of
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