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N-Ethyl-N-benzyl-m-toluidine
Categories:
Colorants & Intermediates

N-Ethyl-N-benzyl-m-toluidine

Alias
EBMT / N-Benzyl-N-ethyl-3-methylaniline / N-Ethyl-N-(3-methylphenyl)benzylamine / N-Benzyl-N-ethyl-m-toluidine
CAS No.
Molecular Formula
C16H19N
Structure
N-Ethyl-N-benzyl-m-toluidine Chemical Structure
Product Details

Product Overview

Product Summary

N-Ethyl-N-benzyl-m-toluidine, also known as N-ethyl-N-benzyl-3-methylaniline, has molecular formula C16H19N, molecular weight 225.34 and CAS number 119-94-8. It is a colorless to light yellow transparent liquid at room temperature with an assay (GC) of ≥98.0% and a refractive index of 1.5870 (see specifications for flash point and related data). Compared with N-ethyl-N-benzylaniline (CAS 92-59-1, molecular formula C15H17N), this product carries one additional methyl group at the 3-position of the ring: the methyl substituent on the m-toluidine scaffold modulates dye shade, shifting it toward red or purple (finished-dye performance is subject to testing of the finished dye). The product is used in synthesis routes for triphenylmethane basic dyes and certain azo cationic dyes.

Usage

Used in dyes and fine chemicals as one of the main intermediates for synthesizing basic and cationic dyes. Structurally similar to N-ethyl-N-benzylaniline, with the methyl substituent on the m-toluidine scaffold modulating dye shade toward red or purple (finished-dye performance is subject to testing of the finished dye). Primarily used in the synthesis of triphenylmethane basic dyes and certain azo cationic dyes, with important applications in acrylic fiber dyeing. The aromatic tertiary amine structural unit participates in subsequent condensation and coupling reactions to construct the chromophoric backbone of dye molecules.
Applications

Applications by Industry

Triphenylmethane Basic Dye Synthesis

Used in triphenylmethane basic dye synthesis; the aromatic tertiary amine structural unit takes part in condensation and coupling reactions that build the chromophoric backbone of the dye molecule. Figures such as assay (GC ≥98.0%) and impurities N-ethyl-m-toluidine (≤0.5%) and N,N-diethyl-m-toluidine (≤0.5%) are listed under specifications for item-by-item review before charging.

Azo Cationic Dye Direction

Used in the synthesis of certain azo cationic dyes; this direction focuses on the substitution position and purity of the intermediate. Batch data can be confirmed with our sales team during inquiry, and specific routes follow the customer's process.

Dyes for Acrylic Fiber Dyeing

The dye varieties obtained are used for acrylic fiber dyeing; methyl substitution shifts the shade toward red or purple, and shade orientation depends on the specific dye structure and process, with finished-dye shade subject to testing of the finished dye. Selection can be discussed with our sales team together with the downstream process.
Specifications

Technical Specifications

Product Specifications
Appearance Colorless to light yellow transparent liquid
Content (GC) % ≥98.0
N-Ethyl-m-toluidine % ≤0.5
N,N-Diethyl-m-toluidine % ≤0.5
Moisture % ≤0.2
Boiling point °C 161–162
Density g/mL 0.770
Refractive index 1.5870
Flash point °C 162
Logistics

Packaging, Storage & Transport

Packaging

200 kg iron drum; custom packaging available upon request. Sample arrangements and order quantities can be discussed during inquiry, and regular batches are produced against the order schedule.

Storage

Store sealed in a cool, dry, well-ventilated place away from heat, sparks and open flames; avoid direct sunlight

Transport

Transport classification follows the goods transport appraisal report and the carrier's requirements

FAQ

Frequently Asked Questions

What is the relationship to N-ethyl-N-benzylaniline?
The two are structurally similar: this product carries one additional methyl group at the 3-position of the ring (CAS 119-94-8, molecular formula C16H19N), while N-ethyl-N-benzylaniline has none (CAS 92-59-1, C15H17N); methyl substitution shifts the dye shade toward red or purple (finished-dye performance is subject to testing of the finished dye). Distinguish the two by CAS number in inquiries. The two differ in molecular weight by about 14 (CH2), which can serve as a reference checkpoint when verifying incoming goods.
How does methyl substitution affect shade?
The methyl substituent on the m-toluidine scaffold modulates dye shade, shifting it toward red or purple; the specific shade is subject to testing of the finished dye.
Which dye types are the main downstream?
Triphenylmethane basic dyes and certain azo cationic dyes, with the resulting varieties used for acrylic fiber dyeing; the correspondence to specific varieties follows the customer's synthesis routes.
What are the assay and impurity specifications?
Assay (GC) ≥98.0%, N-ethyl-m-toluidine ≤0.5%, N,N-diethyl-m-toluidine ≤0.5%, moisture ≤0.2% (see specifications); production and release inspection follow the specifications on this page, and batch data is confirmed with our sales team during inquiry.
What packaging and order quantities are available?
Standard packaging is a 200 kg iron drum, and custom packaging is available. Sample arrangements and order quantities can be discussed during inquiry; regular batches are produced against the order schedule.
What are the storage and transport requirements?
Store sealed in a cool, dry, well-ventilated place away from heat, sparks and open flames, avoiding direct sunlight; see specifications for flash point and related data. Transport classification follows the goods transport appraisal report and the carrier's requirements.