Online Database of Chemicals from Around the World

N-Cyanoethyl-hydroxyethyl aniline
[CAS# 92-64-8]

List of Suppliers
Tianjin Zhongxin Chem-tech Co., Ltd. China Inquire  
+86 (22) 6688-0623
sales@tjzxchem.com
Chemical manufacturer since 2007
chemBlink standard supplier since 2009
Shanghai Yuanye Bio-Technology Co., Ltd. China Inquire  
+86 (21) 6184-5781
+86 13585604150
shyysw053@163.com
QQ chat
Chemical manufacturer since 2009
chemBlink standard supplier since 2016
Anhui Royal Chemical Co., Ltd. China Inquire  
+86 (25) 8663-9253
zoey.zhao@royal-chem.com
Chemical manufacturer since 2008
chemBlink standard supplier since 2019
Complete supplier list of N-Cyanoethyl-hydroxyethyl aniline
Identification
Classification Organic raw materials >> Hydrocarbon compounds and their derivatives >> Cyclic hydrocarbon
Name N-Cyanoethyl-hydroxyethyl aniline
Synonyms 3-(N-(2-Hydroxyethyl)anilino)propiononitrile
Molecular Structure CAS # 92-64-8, N-Cyanoethyl-hydroxyethyl aniline, 3-(N-(2-Hydroxyethyl)anilino)propiononitrile
Molecular Formula C11H14N2O
Molecular Weight 190.24
CAS Registry Number 92-64-8
EC Number 202-174-5
SMILES C1=CC=C(C=C1)N(CCC#N)CCO
Properties
Density 1.1±0.1 g/cm3, Calc.*, 1.12 g/mL
Index of Refraction 1.581, Calc.*, 1.5705
Boiling Point 380.4±27.0 ºC (760 mmHg), Calc.*, 107-110 ºC (15 mm)
Flash Point 183.9±23.7 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319-H335    Details
Precautionary Statements P261-P264-P264+P265-P271-P280-P302+P352-P304+P340-P305+P351+P338-P319-P321-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Eye irritationEye Irrit.2H319
Specific target organ toxicity - single exposureSTOT SE3H335
SDS Available
up Discovory and Applicatios
N-Cyanoethyl-hydroxyethyl aniline is an organic compound classified as a substituted aniline. It contains a cyanoethyl group and a hydroxyethyl group attached to the nitrogen atom of the aniline structure. The compound has attracted interest in various industrial applications due to its unique chemical properties and potential for modification. The discovery of N-cyanoethyl-hydroxyethyl aniline is part of the broader exploration of amine derivatives, which has been ongoing since the early 20th century.

The synthesis of N-cyanoethyl-hydroxyethyl aniline typically involves the reaction of aniline derivatives with cyanoethylating agents and hydroxyethylating agents. This method has been refined to enhance yields and minimize unwanted by-products, making the compound increasingly accessible for industrial use. The ability to tailor the chemical structure of N-cyanoethyl-hydroxyethyl aniline allows researchers and manufacturers to optimize its properties for specific applications.

One of the primary applications of N-cyanoethyl-hydroxyethyl aniline is in the production of specialty coatings. Its unique structure contributes to improved adhesion and flexibility in coating formulations, making it suitable for use in industries such as automotive, construction, and electronics. The compound’s hydroxyethyl group enhances compatibility with various resins, enabling the development of high-performance coatings that exhibit durability and resistance to environmental degradation.

In addition to coatings, N-cyanoethyl-hydroxyethyl aniline is also utilized in the formulation of adhesives. Its properties allow for enhanced bonding strength and flexibility, which are crucial for applications requiring durable and reliable adhesion. The compound's ability to interact with a variety of substrates makes it a valuable component in both industrial and consumer adhesive products.

Furthermore, N-cyanoethyl-hydroxyethyl aniline has potential applications in the field of organic synthesis. Its structure enables it to participate in a range of chemical reactions, making it a versatile intermediate for synthesizing more complex organic molecules. Researchers have explored its use in the synthesis of pharmaceuticals and agrochemicals, showcasing its significance as a building block in chemical manufacturing.

Despite its potential benefits, safety considerations are essential when working with N-cyanoethyl-hydroxyethyl aniline. As a chemical compound, it may pose risks such as skin irritation or respiratory issues if not handled properly. It is crucial to implement appropriate safety measures, including the use of personal protective equipment and adherence to regulatory guidelines to mitigate potential health hazards.

Recent research has also focused on developing greener synthesis routes for N-cyanoethyl-hydroxyethyl aniline and other related compounds. The principles of green chemistry aim to reduce the environmental impact associated with chemical processes while maintaining the desired properties of the final products. Innovations in synthesis techniques may lead to more sustainable production methods for N-cyanoethyl-hydroxyethyl aniline.

In summary, N-Cyanoethyl-hydroxyethyl aniline is a versatile compound with significant applications in coatings, adhesives, and organic synthesis. Its discovery and ongoing development reflect advancements in organic chemistry and materials science, offering opportunities for new applications and improved methodologies across various industries.
Market Analysis Reports
List of Reports Available for N-Cyanoethyl-hydroxyethyl aniline
Related Products
3-Cyano-6-ethyl-1,2-dihydro-2-oxo-4-pyridinecarboxylic acid ethyl ester  2-Cyanoethyl N,N-diisopropylchlorophosphoramidite  N-(2-Cyanoethyl)-N-[(1,1-dimethylethoxy)carbonyl]glycine methyl ester  2-Cyanoethyl ether  N-[3-[(2-Cyanoethyl)ethylamino]-4-methoxyphenyl]acetamide  N-(2-Cyanoethyl)glycine  N-Cyanoethylglycine ethyl ester  N-(2-Cyanoethyl)glycine methyl ester  5-(2-Cyanoethyl)hydantoin  N-[3-[(2-Cyanoethyl)(2-hydroxyethyl)amino]-4-methoxyphenyl]acetamide  6-Cyano-2-[1-(4-ethyl-3-iodophenyl)-1-methylethyl]-1H-indole-3-carboxylic acid 1,1-dimethylethyl ester  2-(2-Cyanoethyl)isothiourea monohydrochloride  Cyanoethyl methacrylate  N-(2-Cyanoethyl)-2-methylalanine  4-[(2-Cyanoethyl)methylamino]benzaldehyde  2-[2-[4-[(2-Cyanoethyl)methylamino]phenyl]ethenyl]-1,3,3-trimethyl-3H-indolium 1,5-naphthalenedisulfonate (2:1)  N-Cyanoethyl-N-methylaniline  2-Cyanoethylmethyldimethoxysilane  2-(3-(1-Cyanoethyl)-5-methylphenyl)-2-methylpropanenitrile  6-Cyano-2-[1-[4-ethyl-3-[4-(4-morpholinyl)-1-piperidinyl]phenyl]-1-methylethyl]-1H-indole-3-carboxylic acid