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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.

Application

Hydrazine cyanurate may be used to synthesize anhydrous hydrazine via thermolysis.

Other Notes

Reagent for the preparation of anhydrous hydrazine of high purity

pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
Solution behavior of poly (styrene)-B lock-poly (2-vinylpyridine) micelles containing gold nanoparticles
Mossmer S, et al.
Macromolecules, 33.13, 4791- 4798 (2000)
E. Nachbaur et al.
Monatshefte fur Chemie / Chemical Monthly, 102, 1718-1718 (1971)
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)
Ruthenium tris (pyrazolyl) borate diazo complexes: Preparation of aryldiazenido, aryldiazene, and hydrazine derivatives
Albertin, Gabriele, et al.
Inorganic Chemistry, 43.14, 4511-4522 (2004)

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