92283-88-0

Basic information

• Product Name: Benzotriazole1.0
• Synonyms: 1.5;Benzotriazole1.0;2,3-Dianhydro-4,6-O-benzylidene-D-allitol;1,5:2,3-dianhydro-4,6-O-[(R)-phenylMethylene]-D-Allitol;(1aS,3aR,6R,7aR,7bS)-6-Phenylhexahydrooxireno[2',3':4,5]pyrano[3,2-d][1,3]dioxine
• CAS NO: 92283-88-0
• Molecular Formula: C₁₃H₁₄O₄
• Molecular Weight: 234.24786
• Mol File: 92283-88-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Benzotriazole1.0(CAS DataBase Reference)
• NIST Chemistry Reference: Benzotriazole1.0(92283-88-0)
• EPA Substance Registry System: Benzotriazole1.0(92283-88-0)

Safety Data

• Hazardous Substances Data: 92283-88-0(Hazardous Substances Data)

Usage

Description

Benzotriazole1.0 is a versatile chemical compound that serves as an effective corrosion inhibitor and stabilizer in various industrial applications. It is recognized for its ability to protect metals from corrosion and oxidation by forming a thin, stable protective layer on metal surfaces. Furthermore, it is utilized as a stabilizer in the production of plastics, adhesives, and coatings to prevent degradation caused by UV radiation exposure. This environmentally friendly chemical is widely adopted across different industries to enhance the durability and longevity of metal and plastic products.

Uses

Used in Metalworking and Metal Cleaning Industry:
Benzotriazole1.0 is used as a corrosion inhibitor for protecting metals from corrosion and oxidation during metalworking and metal cleaning processes. It forms a thin, stable protective layer on the metal surface, thereby extending the life and maintaining the integrity of the metal components.
Used in Plastics Production:
Benzotriazole1.0 is used as a stabilizer in the production of plastics to prevent degradation due to exposure to UV radiation. This helps in maintaining the quality and durability of plastic products, ensuring their longevity and performance.
Used in Adhesives and Coatings Industry:
Benzotriazole1.0 is used as a stabilizer in the formulation of adhesives and coatings to protect them from degradation caused by UV radiation. This contributes to the enhanced durability and performance of these products, making them more reliable for various applications.

Upstream product

• 65391-44-8 1,5-anhydro-4,6-O-(R)-benzylidene-D-glucitol 
• 65371-07-5 2,3-di-O-p-tolylsulphonyl-4,6-O-benzylidene-1,5-anhydro-D-glucitol 

Downstream Products

• 1117903-21-5 1,5-anhydro-4-O-(2-cyanoethoxydiisopropylaminophosphinyl)-2,3-dideoxy-6-O-(4,4'-dimethoxytrityl)-3-fluoro-2-(thymin-1-yl)-D-altritol 
• 1117903-20-4 1,5-anhydro-2,3-dideoxy-6-O-(4,4'-dimethoxytrityl)-3-fluoro-2-(thymin-1-yl)-D-altritol 
• 1117903-19-1 1,5-anhydro-4,6-O-benzylidene-2,3-dideoxy-3-fluoro-2-(thymin-1-yl)-D-altritol 
• 1117903-18-0 1,5-anhydro-4,6-O-benzylidene-2-deoxy-2-(thymin-1-yl)-D-mannitol 
• 1117903-17-9 1,5-anhydro-4,6-O-benzylidene-2-deoxy-3-O-methanesulfonyl-2-(thymin-1-yl)-D-altritol 
• 1117903-22-6 1,5-anhydro-4-O-(tert-butyldimethylsilyl)-2,3-dideoxy-6-O-(4,4'-dimethoxytrityl)-3-fluoro-2-(thymin-1-yl)-D-altritol 
• 705967-67-5 1,5-anhydro-4,6-O-benzylidene-2-deoxy-2-(adenin-9-yl)-D-altro-hexitol 

Relevant articles and documents

Unusual Stereochemistry in the Copper-catalyses Ring Opening of a Carbohydrate Oxirane with Vinylmagnesium Bromide

The oxirane ring of 4,6-O-benzylidene-1,5:2,3-dianhydro-D-allitol (1) opened regio- and stereo-selectively at C-2 with Me2CuLi and allylmagnesium chloride in the presence of catalytic amounts of CuI.With vinylmagnesium bromide, however, the ring opening of (1) was regioselective but a mixture of stereoisomers (10) and (12) was obtained corresponding to retention and inversion at C-2.A mechanism for the formation of the anomalous retention product (12) is proposed.