Online Database of Chemicals from Around the World

1H-Benzotriazole
[CAS# 95-14-7]

List of Suppliers
Epochem Co., Ltd. China Inquire  
+86 (21) 6760-1595
6760-1597
seth_wang@epochem.com
QQ chat
Chemical manufacturer since 2006
chemBlink standard supplier since 2005
Kelien Water Purification Technology Co., Ltd. China Inquire  
+86 (519) 8366-1998
info@kelien.com
Chemical manufacturer
chemBlink standard supplier since 2005
Jiangsu Bohan Industry Trade Co., Ltd. China Inquire  
+86 (25) 8311-1093
sales@bohanchem.com
Chemical distributor since 2010
chemBlink standard supplier since 2006
CAC Shanghai (Group) Co., Ltd. China Inquire  
+86 (21) 6239-8696
service@cacch.com
Chemical distributor since 1992
chemBlink standard supplier since 2006
Shanghai Nanxiang Reagent Co., Ltd. China Inquire  
+86 (21) 3912-7448
+86 13512139665
xumiao@nx-reagent.com
QQ chat
Chemical manufacturer since 1989
chemBlink standard supplier since 2007
Jinan Huifengda Chemical Co., Ltd. China Inquire  
+86 (531) 8887-2378
jnhfdchem@163.com
Chemical distributor since 2006
chemBlink standard supplier since 2007
Simagchem Corporation China Inquire  
+86 13806087780
sale@simagchem.com
Chemical manufacturer since 2002
chemBlink standard supplier since 2008
Guangzhou Lihold Trading Co., Ltd. China Inquire  
+86 (20) 8255-1269
lihold@lihold.com
Chemical manufacturer since 1992
chemBlink standard supplier since 2008
Complete supplier list of 1H-Benzotriazole
Identification
Classification Catalysts and additives >> UV absorber
Name 1H-Benzotriazole
Synonyms 1,2,3-Benzotriazole
Molecular Structure CAS # 95-14-7 (27556-51-0), 1H-Benzotriazole, 1,2,3-Benzotriazole
Molecular Formula C6H5N3
Molecular Weight 119.12
CAS Registry Number 95-14-7 (27556-51-0)
EC Number 202-394-1
SMILES C1=CC2=NNN=C2C=C1
Properties
Solubility 25 g/L (water 20 ºC)
Density 1.36 g/mL
Melting point 94-99 ºC
Boiling point 204 ºC (15 mmHg)
Flash point 170 ºC
Safety Data
Hazard Symbols symbol symbol   GHS07;GHS09 Warning    Details
Hazard Statements H302-H319-H332-H411-H412    Details
Precautionary Statements P261-P264-P264+P265-P270-P271-P273-P280-P301+P317-P304+P340-P305+P351+P338-P317-P330-P337+P317-P391-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Eye irritationEye Irrit.2H319
Acute toxicityAcute Tox.4H332
Chronic hazardous to the aquatic environmentAquatic Chronic3H412
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Acute toxicityAcute Tox.4H312
Acute toxicityAcute Tox.2H330
Acute toxicityAcute Tox.3H301
Serious eye damageEye Dam.1H318
Specific target organ toxicity - single exposureSTOT SE3H335
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2AH319
Flammable solidsFlam. Sol.1H228
Chronic hazardous to the aquatic environmentAquatic Chronic4H413
SDS Available
up Discovory and Applicatios
1H-Benzotriazole is a chemical compound that belongs to the class of heterocyclic compounds, featuring a fused benzene and triazole ring structure. It was first synthesized in the early 20th century as researchers sought to explore the properties and potential applications of triazole derivatives. The initial discovery of benzotriazole is often attributed to its relevance in the field of coordination chemistry, particularly due to its ability to form stable complexes with various metal ions.

The synthesis of 1H-benzotriazole typically involves the cyclization of ortho-aminobenzoic acid or its derivatives with hydrazine or hydrazine derivatives under acidic conditions. This process yields a compound characterized by its distinctive triazole moiety, which imparts unique chemical properties. The compound exists in two tautomeric forms, but the 1H-benzotriazole form is the more stable and commonly encountered structure in applications.

One of the primary applications of 1H-benzotriazole is in the field of corrosion inhibition. It is widely used as a corrosion inhibitor for metals and alloys, particularly in the protection of copper and its alloys. The compound forms a protective film on metal surfaces, preventing oxidation and deterioration caused by environmental factors. This application is critical in various industries, including automotive, aerospace, and marine, where metal components are exposed to corrosive environments.

In addition to its role in corrosion inhibition, 1H-benzotriazole has found applications in the field of organic synthesis as a building block for various chemical compounds. It serves as an effective reagent in the synthesis of pharmaceuticals, agrochemicals, and dyes. Its ability to participate in various chemical reactions, such as nucleophilic substitutions and cycloadditions, makes it a valuable intermediate in the production of complex organic molecules.

Moreover, 1H-benzotriazole is utilized in the field of photoprotection. It has been shown to absorb ultraviolet (UV) radiation, making it a useful additive in sunscreens and other cosmetic formulations. By absorbing harmful UV rays, it helps protect the skin from damage caused by sun exposure, thus contributing to the effectiveness of personal care products.

Safety considerations are important when handling 1H-benzotriazole. While it is generally considered to have low toxicity, appropriate safety measures should be taken during its handling and use, as exposure may lead to irritation of the skin and eyes. It is essential to follow safety guidelines and use personal protective equipment when working with this compound.

In summary, 1H-benzotriazole is a versatile compound with diverse applications in corrosion inhibition, organic synthesis, and photoprotection. Its discovery and subsequent development have led to significant contributions in various industrial sectors, showcasing its importance as a valuable chemical substance.
Market Analysis Reports
List of Reports Available for 1H-Benzotriazole
Related Products
4-(Benzo[b]thiophen-2-yl)aniline  4-(Benzo[b]thiophen-2-yl)-N-(4-(benzo[d]oxazol-2-yl)phenyl)aniline  4-(1-benzothiophen-2-yl)-N-[4-(1-benzothiophen-2-yl)phenyl]aniline  1-Benzo[b]thiophen-3-yl-2-bromoethan-1-one  N-[1-(2-Benzo[b]thiophenyl)cyclohexyl]piperidine  1-Benzothiophen-2-ylethanol  2H-1-Benzothiopyran-3(4H)-one  Benzothioxanthene dicarboxylic anhydride  2-(Benzothioylthio)acetic acid  1,2,3-Benzotriazin-4(3H)-one  1H-Benzotriazole-1-acetonitrile  Benzotriazole-1-carboxamidinium tosylate  Benzotriazole-5-carboxylic acid  1H-Benzotriazole-1-carboxylic acid methyl ester 3-oxide  Benzotriazole-d4  1H-Benzotriazole-6-sulfonic acid  Benzotriazole-1-yl-oxytripyrrolidinophosphonium hexafluorophosphate  2-(1H-Benzotriazole-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate  2-(1H-Benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate  2H-Benzo[c]-1,2,3-triazolo[4,5-a]phenazine