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550728

Sigma-Aldrich

5-Aminotetrazole

97%

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About This Item

Empirical Formula (Hill Notation):
CH3N5
CAS Number:
Molecular Weight:
85.07
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

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

Signal Word

Danger

Hazard Statements

Hazard Classifications

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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Five different nitrogen-rich salts of trinitrophloroglucinol (H(3)TNPG) have been prepared by the reaction of ammonia, aminoguanidine (AG), carbohydrazide (CHZ), semicarbazide (SCZ) and 5-aminotetrazo (ATZ) with trinitrophloroglucinol in aqueous solution through the heating method of water bath, with the yield up
Ionic liquid-promoted multicomponent synthesis of fused tetrazolo [1, 5-a] pyrimidines as a-glucosidase inhibitors.
Suresh L, et al.
Bioorganic & Medicinal Chemistry Letters, 26(16), 4007-4014 (2016)
J Luznik et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 212(1), 149-153 (2011-07-26)
The use of Zeeman perturbed 14N nuclear quadrupole resonance (NQR) to determine the ν+ and ν-14N lines in polycrystalline samples with several nonequivalent nitrogen atoms was investigated. The 14N NQR line shift due to a weak external Zeeman magnetic field
Jian-Guo Zhang et al.
Journal of molecular modeling, 14(5), 403-408 (2008-03-12)
The pathway and ab initio direct kinetics of the decomposition 5-aminotetrazole (5-ATZ) to HN(3) and NH(2)CN was investigated. Reactant, products and transition state were optimized with MP2 and B3LYP methods using 6-311G** and aug-cc-pVDZ basis sets. The intrinsic reaction coordinate
The reactions of 2-ethoxymethylidene-3-oxo esters and their analogues with 5-aminotetrazole as a way to novel azaheterocycles.
Goryaeva MV, et al.
Beilstein Journal of Organic Chemistry, 11(1), 385-391 (2015)

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