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Merck

550728

5-Aminotetrazole

97%

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About This Item

Empirical Formula (Hill Notation):
CH3N5
CAS Number:
Molecular Weight:
85.07
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
224-581-7
MDL number:
Assay:
97%
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assay

97%

mp

201-205 °C (lit.)

SMILES string

Nc1nnn[nH]1

InChI

1S/CH3N5/c2-1-3-5-6-4-1/h(H3,2,3,4,5,6)

InChI key

ULRPISSMEBPJLN-UHFFFAOYSA-N

General description

5-Aminotetrazole (5-AT) can react with different 2-ethoxymethylidene-3-oxo esters and their analogs to form biologically important azaheterocycles.


pictograms

FlameCorrosion

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Desen. Expl. 4 - Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves



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W C de Bruijn et al.
The Histochemical journal, 16(1), 37-50 (1984-01-01)
Addition of heterocyclic nitrogen compounds to the classical osmium tetroxide postfixation medium, applied after glutaraldehyde fixation, results in enhanced membrane contrast in ultrathin sections of liver tissue. The addition of similar compounds to potassium osmate solutions, results in contrast differences
High-Nitrogen-Based Pyrotechnics: Perchlorate-Free Red-and Green-Light Illuminants Based on 5-Aminotetrazole.
Sabatini JJ and Moretti JD.
Chemistry (Weinheim An Der Bergstrasse, Germany), 19(38), 12839-12845 (2013)
Jian-Guo Zhang et al.
Journal of molecular modeling, 15(1), 67-77 (2008-10-23)
The tautomerism and intramolecular hydrogen shifts of 5-amino-tetrazole in the gas phase were studied in the present work. The minimum energy path (MEP) information of 5-amino-tetrazole was obtained at the CCSD(T)/6-311G**//MP2/6-311G** level of theory. The six possible tautomers of 1H