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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:
Molecular Weight:
130.12
Beilstein:
8778859
EC Number:
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
NACRES:
NA.21

grade

ACS reagent

Quality Level

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

Storage Class Code

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials 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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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)
Proton magnetic resonance spectra of hydrazine salts. Part 1.
Pratt L and Richards RE.
Transactions of the Faraday Society, 49, 744-751 (1953)
Synthesis and Characterization of Salicylaldazine and Its Metal (II) Complexes Derived from Metal (II) Chlorides.
Wazir J.
International Journal of Medical Works (2016)
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)
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)

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