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2-CARBOXYMETHYL-2H-BENZOTRIAZOLE, also known as CMBA, is a versatile benzotriazole derivative with the molecular formula C9H8N3O2. It is widely recognized for its ability to form protective films on metal surfaces, thereby serving as an effective corrosion inhibitor in various industrial applications. Its utility extends beyond corrosion inhibition, as it also functions as a photostabilizer in plastics, rubber, and coatings, safeguarding these materials from UV-induced degradation. Furthermore, CMBA's antimicrobial properties contribute to its multifaceted role as an additive in a range of industrial processes.

4144-68-7

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4144-68-7 Usage

Uses

Used in Metalworking Fluids:
2-CARBOXYMETHYL-2H-BENZOTRIAZOLE is used as a corrosion inhibitor for protecting metal surfaces from corrosion, thereby extending the lifespan of the metal. It achieves this by forming a protective film that shields the metal from corrosive elements.
Used in Water Treatment:
In the water treatment industry, 2-CARBOXYMETHYL-2H-BENZOTRIAZOLE is used as a corrosion inhibitor to prevent the deterioration of metal components and infrastructure, ensuring the longevity and efficiency of water treatment systems.
Used in Oilfield Operations:
2-CARBOXYMETHYL-2H-BENZOTRIAZOLE is utilized as a corrosion inhibitor in oilfield operations to protect the metal equipment and pipelines from the corrosive effects of the environment and the substances they come into contact with.
Used in Plastics, Rubber, and Coatings as a Photostabilizer:
2-CARBOXYMETHYL-2H-BENZOTRIAZOLE is used as a photostabilizer to protect plastics, rubber, and coatings from degradation caused by exposure to UV radiation, maintaining their integrity and performance over time.
Used for Antimicrobial Applications:
Owing to its antimicrobial properties, 2-CARBOXYMETHYL-2H-BENZOTRIAZOLE is used as an additive in various industrial processes to prevent the growth of microorganisms that could compromise the quality and safety of the final product.

Check Digit Verification of cas no

The CAS Registry Mumber 4144-68-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,4 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4144-68:
(6*4)+(5*1)+(4*4)+(3*4)+(2*6)+(1*8)=77
77 % 10 = 7
So 4144-68-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H7N3O2/c12-8(13)5-11-9-6-3-1-2-4-7(6)10-11/h1-4H,5H2,(H,12,13)

4144-68-7 Well-known Company Product Price

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  • Aldrich

  • (CBR00336)  2H-1,2,3-Benzotriazol-2-ylacetic acid  AldrichCPR

  • 4144-68-7

  • CBR00336-1G

  • 1,930.50CNY

  • Detail

4144-68-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Carboxymethyl-2H-benzotriazole

1.2 Other means of identification

Product number -
Other names 2-(2H-Benzo[d][1,2,3]triazol-2-yl)acetic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4144-68-7 SDS

4144-68-7Downstream Products

4144-68-7Relevant academic research and scientific papers

NITROGEN SUBSTITUTED AROMATIC TRIAZOLES AS CORROSION CONTROL AGENTS

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Paragraph 0043, (2017/12/01)

Compositions and methods for inhibiting corrosion of metallic surfaces in contact with an aqueous medium such as copper, copper alloy, and steel surfaces of an open recirculating cooling water system. In certain embodiments, an aromatic triazole having an anionic substituent bonded to a nitrogen atom of the triazole (ANST) is used as the corrosion inhibitor. In other embodiments, the corrosion inhibitor is a reaction product of an aromatic triazole and an aldehyde (ATA).

Fundamental structure-activity relationships associated with a new structural class of respiratory syncytial virus inhibitor

Yu, Kuo-Long,Zhang, Yi,Civiello, Rita L.,Kadow, Kathleen F.,Cianci, Christopher,Krystal, Mark,Meanwell, Nicholas A.

, p. 2141 - 2144 (2007/10/03)

Structure-activity relationships surrounding the dialkylamino side chain of a series of benzotriazole-derived inhibitors of respiratory syncytial virus fusion based on the screening lead 1a were examined. The results indicate that the topology of the side chain is important but the terminus element offers considerable latitude to modulate physical properties.

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