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Sigma-Aldrich

Benzotriazole-5-carboxylic acid

99%

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About This Item

Empirical Formula (Hill Notation):
C7H5N3O2
CAS Number:
Molecular Weight:
163.13
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

form

solid

SMILES string

OC(=O)c1ccc2[nH]nnc2c1

InChI

1S/C7H5N3O2/c11-7(12)4-1-2-5-6(3-4)9-10-8-5/h1-3H,(H,11,12)(H,8,9,10)

InChI key

GUOVBFFLXKJFEE-UHFFFAOYSA-N

Gene Information

human ... GPR109B(8843)

Application

Benzotriazole-5-carboxylic acid was used as bifunctional ligand in solvent induced synthesis of diverse dimensional coordination assemblies of cupric benzotriazole-5-carboxylate. It was also used in hydrothermal synthesis of new coordination polymer, [Zn(Btca)(Phen)]n (H2Btca = benzotriazole-5-carboxylic acid, Phen = 1,10-phenanthroline).

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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Juan Xiao et al.
Inorganic chemistry, 50(21), 11032-11038 (2011-10-11)
Three cupric coordination assemblies [Cu(btca)(H(2)O)(2)] (1), [Cu(btca)(H(2)O)(3.5)](8)·16H(2)O (2), and [Cu(2.5)(btca)(1.5)(Hbtca)(0.5)(μ-Cl)(0.5)(μ(3)-OH)(H(2)O)]·H(2)O (3) have been solvothermally synthesized by cupric salts and a bifunctional ligand benzotriazole-5-carboxylic acid (H(2)btca) in different solvent medium. These complexes were structurally characterized by X-ray diffraction analyses and further
Fuminori Ohsawa et al.
Journal of medicinal chemistry, 56(5), 1865-1877 (2013-02-09)
We have reported that retinoid X receptor (RXR) partial agonist 1-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthyl)-1H-benzotriazole-5-carboxylic acid (CBt-PMN, 4a) shows a significant antidiabetes effect in the KK-A(y) type 2 diabetes model mice, with reduced side effects compared to RXR full agonists. To elucidate the mechanism
Hydrothermal synthesis and crystal structure of a new 2D metal-organic framework:[Zn (Btca)(Phen)] n (H2Btca= benzotriazole-5-carboxylic acid, phen= 1, 10-phenanthroline).
Lu RY and Han ZB.
Russian Journal of Coordination Chemistry, 37(3), 172-175 (2011)
H Hoffmann et al.
Archiv der Pharmazie, 322(8), 457-459 (1989-08-01)
The 1H-benzotriazolecarboxylic acids 1 and 2 were stable towards oxidative metabolism as well in vitro as in vivo. In the in vivo studies 2.25% of the ester glucuronide of 1H-benzotriazole-5-carboxylic acid was found in urine.

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