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455865

Sigma-Aldrich

Hydrazine sulfate salt

99.999% trace metals basis

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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:
12352100
PubChem Substance ID:
24869089
NACRES:
NA.22

Assay

99.999% trace metals basis

form

solid

mp

254 °C (lit.)

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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Product No.
Description
Pricing

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

Certificates of Analysis (COA)

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Hepatic carcinogenesis in CBA-Cb-Se mice and Cb-Se rats by isonicotinic acid hydrazide and hydrazine sulfate.
L Severi et al.
Journal of the National Cancer Institute, 41(2), 331-349 (1968-08-01)
Fluorinated polyoxadiazole for high-temperature polymer electrolyte membrane fuel cells.
Dominique G and Nunes SP.
Journal of Membrane Science, 321(1), 114-122 (2008)
Tumorigenesis studies with 1,2-dimethylhydrazine dihydrochloride, hydrazine sulfate, and isonicotinic acid in golden hamsters.
B Toth
Cancer research, 32(4), 804-807 (1972-04-01)
Azo Compounds. 1 A Re-examination of the Structure of the Product from the Reaction of Heptane-2, 6-dione with Hydrazine Sulfate and Sodium Cyanide in Dilute Solution.
Overberger CG and Marks BS.
Journal of the American Chemical Society, 77(15), 4097-4100 (1955)
Ranendu Sekhar Das et al.
Dalton transactions (Cambridge, England : 2003), 42(11), 4068-4080 (2013-01-24)
PVP capped platinum nano particles (PNP) of 5 nm diameter were prepared and characterized as homogeneous and of spherical nature. At physiological pH range (6.0-8.0), these PNP catalyze the deoxygenation of phenoxazine group containing resazurin (1) by hydrazine. The observed
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