16584-00-2 Usage
Description
2-METHYL-2H-BENZOTRIAZOLE is a chemical compound that belongs to the benzotriazole class. It is known for its wide-ranging applications as a corrosion inhibitor and UV absorber in the production of plastics, rubbers, and coatings. Additionally, it functions as a stabilizer for metal protection and acts as an anticorrosive agent in various industrial and commercial products. Despite its utility, it is recognized for its potential environmental toxicity and is classified as a hazardous chemical. Its molecular structure and properties render it suitable for a variety of industrial applications, particularly for maintaining the integrity and durability of materials that are exposed to harsh conditions.
Uses
Used in Chemical Industry:
2-METHYL-2H-BENZOTRIAZOLE is used as a corrosion inhibitor for protecting metals from degradation, which is crucial in various industrial processes and for the longevity of metal components.
Used in Plastics and Rubber Industry:
It serves as a UV absorber, helping to prevent the degradation of plastics and rubbers caused by exposure to ultraviolet radiation, thereby enhancing their durability and performance.
Used in Coatings Industry:
2-METHYL-2H-BENZOTRIAZOLE is used as a stabilizer in the formulation of coatings to protect the coated surfaces from corrosion and extend their service life.
Used in Environmental Protection:
Despite its potential environmental toxicity, it is used in controlled environments and applications where its benefits outweigh the risks, with proper handling and disposal measures in place to mitigate any hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 16584-00-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,8 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16584-00:
(7*1)+(6*6)+(5*5)+(4*8)+(3*4)+(2*0)+(1*0)=112
112 % 10 = 2
So 16584-00-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3/c1-10-8-6-4-2-3-5-7(6)9-10/h2-5H,1H3
16584-00-2Relevant articles and documents
Sodium hydrogen exchanger inhibitory activity of benzotriazole derivatives
Singh, Dhandeep,Silakari, Om
, p. 183 - 189 (2016/10/25)
Series of benzotriazole derivatives were synthesized and evaluated for their Sodium hydrogen exchanger-1 inhibitory potential. All compounds inhibit Sodium hydrogen exchanger-1 in the in-vitro platelet swelling assay. This is perhaps the first report of NHE-1 inhibitory activity of benzotriazole. The 1-alkyl benzotriazole derivatives were found to be more active than the 2-alkyl isomers. The activity increases with increase in chain length of alkyl moiety. Potency increased from that of benzotriazole (IC50= 192.68 μM) to heptyl derivative (compound 13; IC50= 59.23 μM). Introduction of electronegative oxygen atom further increased potency as shown by the benzoyl (compound 16, IC50= 51.57 μM) and sulfonyl groups (compound 17, IC50= 50.89 μM; compound 18, IC50= 49.95 μM).
Organic reactions in ionic liquids: An efficient method for the N-alkylation of benzotriazole
Le, Zhang-Gao,Chen, Zhen-Chu,Hu, Yi,Zheng, Qin-Guo
, p. 344 - 346 (2007/10/03)
The N-alkylation of benzotriazole with alkyl halides proceeds efficiently in the presence of potassium hydroxide in ionic liquid 1-butyl-3- methylimidazolium tetrafluoroborate ([Bmim][BF4]).
SELECTIVE ALKYLATIONS OF 1,2,4-TRIAZOLE AND BENZOTRIAZOLE IN THE ABSENCE OF SOLVENT
Abenhaim, David,Diez-Barra, Enrique,Hoz, Antonio de la,Loupy, Andre,Sanchez-Migallon, Ana
, p. 793 - 802 (2007/10/02)
Alkylation of 1,2,4-triazole and benzotriazole has been performed either in basic media under solvent free phase transfer catalysis conditions or in the absence of base by conventional and microwave heating.Several parameters affecting the selectivity have been studied.In the case of triazole alkylation, microwave irradiation produces specific (non thermal) effects both on reactivity and selectivity.
