Skip to Content
Merck

H4766

Hydrazine hemisulfate salt

≥98%

Synonym(s):

Dihydrazine sulfate, Dihydrazinium sulfate

Sign In to View Organizational & Contract Pricing.

Select a Size

All Photos(2)

About This Item

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

Product Name

Hydrazine hemisulfate salt, ≥98%

InChI key

DBLJAFVPFHRQSP-UHFFFAOYSA-N

InChI

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

SMILES string

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

assay

≥98%

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

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).

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

Storage Class

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCZ7405
MKCW2077
MKCW0554
MKCT1640
MKCT7913

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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
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
John M Keith
The Journal of organic chemistry, 77(24), 11313-11318 (2012-12-12)
Various pyridine, quinoline, isoquinoline, and pyrimidine N-oxides were converted to their corresponding α-N-aryltriflamidoheteroarenes in good yield by treatment with N-aryltriflimides, both neat and in solution, at temperatures ranging from rt to 100 °C.
Nadia A Mohamed et al.
Molecules (Basel, Switzerland), 17(12), 13969-13988 (2012-11-28)
Twelve novel intrinsically colored wholly aromatic azopolyamide-hydrazides containing various proportions of para- and meta-phenylene units were successfully synthesized by a low temperature (-10 °C) solution polycondensation reaction of either 4-amino-3-hydroxybenzhydrazide (4A3HBH) or 3-amino-4-hydroxybenzhydrazide (3A4HBH) with an equimolar amount of either
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service