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N-Isopropylaniline
[CAS# 768-52-5]

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Complete supplier list of N-Isopropylaniline
Identification
Classification Organic raw materials >> Amino compound >> Cycloalkylamines, aromatic monoamines, aromatic polyamines and derivatives and salts
Name N-Isopropylaniline
Synonyms N-(1-Methylethyl)benzenamine; N-Phenylisopropylamine; N-IPA
Molecular Structure CAS # 768-52-5, N-Isopropylaniline, N-(1-Methylethyl)benzenamine, N-Phenylisopropylamine, N-IPA
Molecular Formula C9H13N
Molecular Weight 135.21
CAS Registry Number 768-52-5
EC Number 212-196-7
SMILES CC(C)NC1=CC=CC=C1
Properties
Density 0.934
Boiling point 202 ºC
Refractive index 1.539
Flash point 87.7 ºC
Water solubility <0.01 g/100 mL at 21 ºC
Safety Data
Hazard Symbols symbol symbol   GHS06;GHS07 Danger    Details
Hazard Statements H302-H315-H319-H330-H335    Details
Precautionary Statements P260-P261-P264-P264+P265-P270-P271-P273-P280-P284-P301+P317-P302+P352-P304+P340-P305+P351+P338-P316-P319-P320-P321-P330-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Eye irritationEye Irrit.2H319
Acute toxicityAcute Tox.2H330
Specific target organ toxicity - single exposureSTOT SE3H335
Skin irritationSkin Irrit.2H315
Skin sensitizationSkin Sens.1H317
Reproductive toxicityRepr.2H361
Acute toxicityAcute Tox.4H332
Transport Information UN 2810
SDS Available
up Discovory and Applicatios
N-Isopropylaniline, an organic compound with the molecular formula C₉H₁₃N, belongs to the class of secondary amines. It is characterized by the presence of an isopropyl group attached to the nitrogen atom of an aniline structure. The compound was first synthesized in the late 19th century as chemists began exploring the properties and reactions of amines and their derivatives. Its structural features allow it to participate in a variety of chemical reactions, leading to numerous applications in various industries.

The synthesis of N-isopropylaniline typically involves the alkylation of aniline with isopropyl halides or through the reductive amination of acetophenone using isopropylamine. This straightforward synthetic route has made N-isopropylaniline readily available for research and industrial purposes. Its unique properties, including the ability to act as a nucleophile due to the electron-donating effect of the isopropyl group, make it a valuable intermediate in organic synthesis.

One of the primary applications of N-isopropylaniline is in the production of dyes and pigments. It serves as a key building block in the synthesis of various azo dyes, which are widely used in textiles, food, and cosmetics due to their vibrant colors and stability. The electron-donating properties of the isopropyl group enhance the dyeing performance, making N-isopropylaniline a crucial component in the dye industry.

In addition to its role in dye manufacturing, N-isopropylaniline is also utilized in the formulation of agricultural chemicals, particularly in the synthesis of herbicides and pesticides. Its reactivity enables the formation of various herbicidal agents, contributing to the development of effective crop protection strategies. The compound’s ability to enhance the bioavailability and effectiveness of these chemicals has made it an essential part of agrochemical formulations.

Furthermore, N-isopropylaniline finds application in the production of pharmaceuticals and fine chemicals. It serves as a precursor for the synthesis of various biologically active compounds, including pharmaceuticals and therapeutic agents. The compound's versatility in organic synthesis makes it a valuable intermediate in the pharmaceutical industry, aiding in the development of new drugs and treatments.

Despite its useful applications, N-isopropylaniline must be handled with care due to potential health risks associated with exposure. It is classified as harmful if inhaled, ingested, or if it comes into contact with skin. Proper safety precautions should be implemented during its use in industrial and laboratory settings to mitigate any associated hazards.

In summary, N-isopropylaniline is an important organic compound with a range of applications across various industries, including dye production, agriculture, and pharmaceuticals. Its discovery and subsequent utilization have contributed significantly to advancements in organic synthesis and chemical manufacturing, highlighting its role as a valuable building block in modern chemistry.
Market Analysis Reports
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