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216046

Sigma-Aldrich

Hydrazine sulfate salt

ACS reagent, ≥99.0%

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About This Item

Linear Formula:
NH2NH2 · H2SO4
CAS Number:
10034-93-2
Molecular Weight:
130.12
Beilstein:
8778859
EC Number:
233-110-4
MDL number:
MFCD00044873
UNSPSC Code:
12352300
PubChem Substance ID:
24852935
NACRES:
NA.21

grade

ACS reagent

Quality Level

200

Assay

≥99.0%

form

powder, crystals or chunks

impurities

≤0.005% insolubles

ign. residue

≤0.05%

pH

1.3 (52 g/L)

mp

254 °C (lit.)

anion traces

chloride (Cl-): ≤0.005%

cation traces

Fe: ≤0.001%
heavy metals: ≤0.002% (by ICP)

SMILES string

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

InChI

1S/H4N2.H2O4S/c1-2;1-5(2,3)4/h1-2H2;(H2,1,2,3,4)

InChI key

ZGCHATBSUIJLRL-UHFFFAOYSA-N

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General description

Hydrazine sulfate salt is a potential anticachexia agent for treating cancer patients.

Application

Hydrazine sulfate salt may be used in the synthesis of symmetrically 3,5-disubstituted 4-amino-1,2,4-triazoles, poly(1,3,4-oxadiazole) copolymers and salicylaldazine.

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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 - Eye Dam. 1 - Skin Corr. 1 - Skin Sens. 1

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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Gold nanoparticles formation in the aqueous system of gold (III) chloride complex ions and hydrazine sulfate-kinetic studies.
Streszewski B, et al.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 397, 63-72 (2012)
Synthesis and Characterization of Salicylaldazine and Its Metal (II) Complexes Derived from Metal (II) Chlorides.
Wazir J.
International Journal of Medical Works (2016)
Proton magnetic resonance spectra of hydrazine salts. Part 1.
Pratt L and Richards RE.
Transactions of the Faraday Society, 49, 744-751 (1953)
A simple one step synthesis of new 3, 5?disubstituted?4?amino?1, 2, 4?triazoles
Bentiss F, et al.
Journal of Heterocyclic Chemistry, 36(1), 149-152 (1999)
One-pot method for the synthesis of sulfonated poly (1, 3, 4-oxadiazoles) based on 4, 4?-oxydibenzoic acid
Yashchenko VS, et al.
Polymer Science, Series B, 58(5), 529-540 (2016)
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