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53828

Sigma-Aldrich

Hydrazine cyanurate

≥99.0% (T)

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About This Item

Linear Formula:
NH2NH2 · C3H3N3O3
CAS Number:
18836-29-8
Molecular Weight:
161.12
EC Number:
242-618-5
MDL number:
MFCD00043299
UNSPSC Code:
12352100
PubChem Substance ID:
57651452
NACRES:
NA.22

Quality Level

100

Assay

≥99.0% (T)

SMILES string

NN.Oc1nc(O)nc(O)n1

InChI

1S/C3H3N3O3.H4N2/c7-1-4-2(8)6-3(9)5-1;1-2/h(H3,4,5,6,7,8,9);1-2H2

InChI key

REWJAYUHYGWDJT-UHFFFAOYSA-N

General description

Hydrazine cyanurate (HC) is a stable source of N2H4 for use in various nitridation reactions. HC can be synthesized from the reaction between cyanuric acid and N2H4.[1]

Application

Hydrazine cyanurate may be used to synthesize anhydrous hydrazine via thermolysis.[2][3]

Other Notes

Reagent for the preparation of anhydrous hydrazine of high purity[4]

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301 + H311 + H331

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral

Storage Class Code

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

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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Certificates of Analysis (COA)

Lot/Batch Number
BCBN8594V
BCBC0082V
BCBC0082
1056653
43005/1

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Hydrazine cyanurate as a nitrogen source for thin nitride film growth
Kropewnicki TJ and Kohl PA
Journal of Vacuum Science & Technology. A, Vacuum, Surfaces, And Films, 16.1 , 139-144 (1998)
Ruthenium tris (pyrazolyl) borate diazo complexes: Preparation of aryldiazenido, aryldiazene, and hydrazine derivatives
Albertin, Gabriele, et al.
Inorganic Chemistry, 43.14, 4511-4522 (2004)
Development of a 18F-Labeled Tetrazine with Favorable Pharmacokinetics for Bioorthogonal PET Imaging
Denk, Christoph, et al.
Angewandte Chemie (International Edition in English), 53.36, 9655-9659 (2014)
E. Nachbaur et al.
Monatshefte fur Chemie / Chemical Monthly, 102, 1718-1718 (1971)
Solution behavior of poly (styrene)-B lock-poly (2-vinylpyridine) micelles containing gold nanoparticles
Mossmer S, et al.
Macromolecules, 33.13, 4791- 4798 (2000)

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