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4-(1H-1,2,3-Benzotriazol-1-ylmethyl)phenylamine, commonly known as UV-326, is a chemical compound that serves as a UV stabilizer in various materials. It is effective in absorbing and dissipating harmful UV radiation, thus preventing degradation and discoloration of the materials it is applied to. 4-(1H-1,2,3-BENZOTRIAZOL-1-YLMETHYL)PHENYLAMINE is characterized by its ability to enhance the durability and longevity of products in which it is incorporated.

129075-89-4

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129075-89-4 Usage

Uses

Used in Plastics Industry:
4-(1H-1,2,3-Benzotriazol-1-ylmethyl)phenylamine is used as a UV stabilizer for plastics to protect them from the damaging effects of ultraviolet light, thereby extending their service life and maintaining their aesthetic properties.
Used in Coatings Industry:
In the coatings industry, 4-(1H-1,2,3-Benzotriazol-1-ylmethyl)phenylamine is used as a UV stabilizer to prevent the fading and degradation of coatings when exposed to sunlight, ensuring their color retention and durability.
Used in Rubber Products:
4-(1H-1,2,3-Benzotriazol-1-ylmethyl)phenylamine is used as a UV stabilizer in rubber products to shield them from UV-induced degradation, which helps in maintaining the physical properties and appearance of rubber items.
Used in Adhesives and Sealants Production:
4-(1H-1,2,3-Benzotriazol-1-ylmethyl)phenylamine is used as an additive in the production of adhesives and sealants to improve their resistance to UV radiation, thus enhancing their performance and lifespan.
However, it is important to note that there are concerns regarding the potential environmental and health risks associated with the use of 4-(1H-1,2,3-Benzotriazol-1-ylmethyl)phenylamine. This has led to regulations and restrictions in some regions to mitigate these risks. As such, its usage in various applications needs to be carefully managed to ensure the safety of both the environment and human health.

Check Digit Verification of cas no

The CAS Registry Mumber 129075-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,0,7 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 129075-89:
(8*1)+(7*2)+(6*9)+(5*0)+(4*7)+(3*5)+(2*8)+(1*9)=144
144 % 10 = 4
So 129075-89-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H12N4/c14-11-7-5-10(6-8-11)9-17-13-4-2-1-3-12(13)15-16-17/h1-8H,9,14H2

129075-89-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(benzotriazol-1-ylmethyl)aniline

1.2 Other means of identification

Product number -
Other names 4-(1H-1,2,3-benzotriazol-1-ylmethyl)phenylamine

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:129075-89-4 SDS

129075-89-4Relevant academic research and scientific papers

N-butyllithium-mediated reactions of 1-(2-azidoarylmethyl)-1H- benzotriazoles with alkyl halides

Kim, Taehoon,Kim, Kyongtae

experimental part, p. 98 - 111 (2010/04/23)

(Chemical Equation Presented) Treatment of 1-(2-azidoarylmethyl)-1H- benzotriazoles (6) with n-BuLi (2.5 equiv.) in THF at -78°C, followed by an addition of alkyl halides such as allyl, benzyl, and ethyl bromides with stirring for 2 h at room temperature afforded 2-(dialkylamino)-3-(benzotriazol- 1-yl)-2H-indazoles (8), 3-(benzotriazol-1-yl)-2H-indazoles (9), 2-[(benzotriazol-1-yl)methyl]arylamine (10), and 2-[(benzotriazol-1-yl)(alkyl) methyl]arylamine (11).

Benzotriazole Mediated Synthesis of Methylenebisanilines

Katritzky, Alan R.,Lan, Xiangfu,Lam, Jamshed N.

, p. 341 - 346 (2007/10/02)

Methylenebisanilines and methylenebis(N,N-dialkylaniline)s are prepared by the reactions of 1-hydroxymethylbenzotriazole with anilines and with N,N-dialkylanilines under acidic conditions.Isolation of the intermediate 4-(benzotriazol-1-ylmethyl)anilines and the N,N-dialkyl analogues and their reactions with anilines allow the efficient preparation of both symmetrical and unsymmetrical members of both product classes.

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