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Sigma-Aldrich

1H-Tetrazole-5-acetic acid

96%

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About This Item

Empirical Formula (Hill Notation):
C3H4N4O2
CAS Number:
Molecular Weight:
128.09
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

96%

mp

180-183 °C (lit.)

SMILES string

OC(=O)Cc1nnn[nH]1

InChI

1S/C3H4N4O2/c8-3(9)1-2-4-6-7-5-2/h1H2,(H,8,9)(H,4,5,6,7)

InChI key

JUNAPQMUUHSYOV-UHFFFAOYSA-N

General description

1H-Tetrazole-5-acetic acid H2tza) can be prepared from ethyl 2-(1H-tetrazol-5-yl)acetate.

Application

1H-Tetrazole-5-acetic acid(H2tza) may be used in the preparation of:
  • 5-(trinitromethyl)-2H-tetrazole
  • N-(furan-2yl methyl)-2-(1H-tetrazol-5-yl)acetamide
  • tetrazolium based ionic liquid

It may also be used as a bifunctional ligand for the synthesis of novel copper(II) and nickel(II) complexes.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

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)

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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Microwave assisted synthesis of indole and furan derivatives possessing good anti-inflammatory and analgesic activity.
Sondhi SM, et al.
Indian J. Chem. B, 46(11), 1848-1848 (2007)
New Copper (II) and Nickel (II) Complexes with Bifunctional Tetrazolate-5-carboxylate Ligands: Syntheses, Crystal Structures, and Magnetic Properties.
Wu AQ, et al.
Australian Journal of Chemistry, 62(12), 1622-1630 (2010)
Synthesis and characterization of silver and gold nanoparticles in ionic liquid.
Singh P, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 73(1), 218-220 (2009)
Energetic High-Nitrogen Compounds: 5-(Trinitromethyl)-2H-tetrazole and-tetrazolates, Preparation, Characterization, and Conversion into 5-(Dinitromethyl) tetrazoles.
Haiges R and Christe KO.
Inorganic Chemistry, 52(12), 7249-7260 (2013)

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