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Bis-[2-hydroxy-5-methyl-3-(benzotriazol-2-yl)-phenyl]-methane is a chemical compound known for its ability to absorb and dissipate ultraviolet (UV) radiation. It is characterized by its molecular structure that includes hydroxy, methyl, and benzotriazol-yl groups attached to a phenyl ring, which contribute to its UV filtering properties. Bis-[2-hydroxy-5-methyl-3-(benzotriazol-2-yl)-phenyl]-methane is widely recognized for its use in various applications due to its protective capabilities against UV-induced damage.

30653-05-5

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30653-05-5 Usage

Uses

Used in Cosmetics and Personal Care Products:
Bis-[2-hydroxy-5-methyl-3-(benzotriazol-2-yl)-phenyl]-methane is used as a UV filter to protect the skin from harmful UV radiation. It is incorporated into sunscreens and other skincare products to prevent sunburn, premature aging, and reduce the risk of skin cancer caused by excessive UV exposure.
Used in Industrial Applications:
In the industrial sector, Bis-[2-hydroxy-5-methyl-3-(benzotriazol-2-yl)-phenyl]-methane is used as a UV stabilizer for plastics and coatings. It helps to prevent the degradation of these materials when exposed to sunlight, thereby extending their lifespan and maintaining their aesthetic and functional properties.
Used in Environmental Considerations:
Bis-[2-hydroxy-5-methyl-3-(benzotriazol-2-yl)-phenyl]-methane is also used in the context of environmental impact assessment. Due to concerns about its potential to bioaccumulate and persist in the environment, it is subject to regulation in some regions. This application involves monitoring and managing its use to minimize ecological risks and ensure responsible chemical stewardship.

Check Digit Verification of cas no

The CAS Registry Mumber 30653-05-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,5 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 30653-05:
(7*3)+(6*0)+(5*6)+(4*5)+(3*3)+(2*0)+(1*5)=85
85 % 10 = 5
So 30653-05-5 is a valid CAS Registry Number.

30653-05-5SDS

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-(benzotriazol-2-yl)-6-[[3-(benzotriazol-2-yl)-2-hydroxy-5-methylphenyl]methyl]-4-methylphenol

1.2 Other means of identification

Product number -
Other names Ultraviolet Absorbent UV-360

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:30653-05-5 SDS

30653-05-5Downstream Products

30653-05-5Relevant academic research and scientific papers

Method for preparing benzotriazole-alkylene bisphenol compound

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Paragraph 0030; 0031, (2017/02/02)

The invention discloses a method for preparing a benzotriazole-alkylene bisphenol compound, and is characterized in that the method comprises the following steps: step 1, dissolving a first part of UV-P, dialkyl amine and paraformaldehyde in an alcohol solvent, and carrying out a stirring reaction at the temperature of 95-105 DEG C; step 2, after stirring for 24 h, drying the alcohol solvent by distillation in vacuum, to obtain an intermediate; step 3, dissolving the intermediate and a second part of UV-P in an aromatic hydrocarbon or alkane solvent, adding sodium methylate, heating the solution to 140-150 DEG C, and carrying out a reflux reaction for 10 h; step 4, after the reaction is finished, steaming out a part of the aromatic hydrocarbon or alkane solvent, and cooling and crystallizing to obtain a crude product; and step 5, recrystallizing the crude product to obtain a white solid, wherein the UV-P has the structural formula represented by the formula I, the white solid has the structural formula represented by the formula II. The preparation method has the beneficial effect of good yield.

Low-emulsifier or emulsifier-free systems of the oil-in-water type with a content of stabilizers and an amino-substituted hydroxybenzophenone

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, (2008/06/13)

Cosmetic or dermatological preparations which represent finely disperse systems of the oil-in-water type, comprising a) an oil phase, b) a water phase, c) one or more stabilizers, d) at most 2.00% by weight of one or more emulsifiers, and e) an amino-substituted hydroxybenzophenone of the formula I

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