N-Ethyl-3-methylaniline
[CAS# 102-27-2]

Identification

• Classification: Organic raw materials >> Amino compound >> Cycloalkylamines, aromatic monoamines, aromatic polyamines and derivatives and salts
• Name: N-Ethyl-3-methylaniline
• Synonyms: N-Ethyl-m-toluidine
• Molecular Formula: C₉H₁₃N
• Molecular Weight: 135.21
• CAS Registry Number: 102-27-2
• EC Number: 203-019-4
• SMILES: CCNC1=CC=CC(=C1)C

Properties

• Density: 0.957
• Boiling point: 221 ºC
• Refractive index: 1.545-1.547
• Flash point: 89 ºC
• Water solubility: 1131 mg/L (20 ºC)

Safety Data

• Hazard Symbols: GHS06;GHS07 Denger
• Hazard Statements: H301-H311-H315-H319-H331-H335-H412
• Precautionary Statements: P261-P262-P264-P264+P265-P270-P271-P273-P280-P301+P316-P302+P352-P304+P340-P305+P351+P338-P316-P319-P321-P330-P332+P317-P337+P317-P361+P364-P362+P364-P403+P233-P405-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Acute toxicity	Acute Tox.	3	H311
Acute toxicity	Acute Tox.	3	H301
Acute toxicity	Acute Tox.	3	H331
Skin irritation	Skin Irrit.	2	H315
Specific target organ toxicity - single exposure	STOT SE	3	H335
Eye irritation	Eye Irrit.	2	H319
Chronic hazardous to the aquatic environment	Aquatic Chronic	3	H412
Eye irritation	Eye Irrit.	2A	H319
Acute toxicity	Acute Tox.	2	H310
Acute toxicity	Acute Tox.	4	H302
Acute toxicity	Acute Tox.	2	H330

• Transport Information: UN 2754

Discovory and Applicatios

N-Ethyl-3-methylaniline, also known as N-ethyl-m-toluidine, is an organic compound with the chemical formula C9H13N. This chemical structure consists of an aniline group (C6H5NH2) where the nitrogen is substituted by an ethyl group (C2H5) and a methyl group (CH3) is attached to the benzene ring at the meta position relative to the amine group. The discovery of this compound is tied to the broader study of aniline derivatives, which have been widely explored for their applications in dyes, polymers, and pharmaceuticals.

The synthesis of N-ethyl-3-methylaniline typically involves the alkylation of 3-methylaniline (m-toluidine) with an ethylating agent, such as ethyl bromide or ethyl chloride, in the presence of a base. The reaction proceeds through nucleophilic substitution, where the nitrogen atom in the aniline group acts as a nucleophile, bonding with the ethyl group. This relatively straightforward synthetic route allows for the efficient production of N-ethyl-3-methylaniline in both laboratory and industrial settings.

One of the primary applications of N-ethyl-3-methylaniline is in the manufacture of dyes and pigments. Aniline derivatives, such as N-ethyl-3-methylaniline, serve as important intermediates in the production of azo dyes, which are characterized by their vivid colors and wide range of applications. These dyes are used in textiles, leather, plastics, and printing inks. The presence of the ethyl and methyl groups in N-ethyl-3-methylaniline modifies the electronic properties of the aniline core, enabling the creation of dyes with specific shades and improved stability. By controlling the substituents on the aromatic ring, chemists can fine-tune the color and performance characteristics of these dyes to meet industry demands.

In addition to its role in dye production, N-ethyl-3-methylaniline is used in the synthesis of polymers and resins. The compound can act as a precursor in the production of specialty polymers, where the aniline group contributes to the polymer’s thermal and chemical resistance. Polymers derived from aniline derivatives often exhibit excellent electrical conductivity, making them valuable in applications such as coatings for electronics and anti-static materials. The inclusion of N-ethyl-3-methylaniline in these polymer systems helps enhance their mechanical properties and durability, especially in environments that require resistance to heat and corrosion.

N-ethyl-3-methylaniline also finds application in the field of organic synthesis as a reagent and intermediate. Its reactivity allows it to participate in various chemical transformations, including acylation, sulfonation, and oxidation reactions. In medicinal chemistry, aniline derivatives have been explored for their potential as therapeutic agents, and compounds like N-ethyl-3-methylaniline are used in the development of pharmaceuticals that target specific biological pathways. Although N-ethyl-3-methylaniline itself is not a drug, its structural framework can be modified to create analogs with desired bioactivity.

Another key area where N-ethyl-3-methylaniline is employed is in the production of rubber chemicals. It is used as a building block for antioxidants and vulcanization accelerators, which improve the performance and longevity of rubber products. The compound helps stabilize rubber during processing and extends the material’s life by protecting it from oxidative degradation. These properties are particularly important in the automotive and industrial sectors, where rubber components are exposed to harsh conditions.

While N-ethyl-3-methylaniline has valuable applications, its handling requires caution due to potential health risks. Like many aniline derivatives, it can be toxic if inhaled, ingested, or absorbed through the skin. Prolonged exposure can lead to methemoglobinemia, a condition in which the blood's ability to carry oxygen is impaired. Therefore, strict safety measures, including the use of personal protective equipment and proper ventilation, are essential when working with this compound in both laboratory and industrial settings.

In conclusion, N-ethyl-3-methylaniline is a versatile chemical that plays a significant role in the production of dyes, polymers, and other industrial products. Its unique structure allows for its use in various chemical processes, from dye synthesis to the manufacture of rubber additives. While its applications are widespread, safety considerations are paramount due to the potential health hazards associated with aniline compounds. Ongoing research into the properties and potential new applications of N-ethyl-3-methylaniline ensures that it remains a valuable chemical in various industries.