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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

Certificates of Analysis (COA)

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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
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
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
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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