13021-14-2

Basic information

• Product Name: 2 4 6-TRIMETHYL-N-METHYLANILINE 97
• Synonyms: 2 4 6-TRIMETHYL-N-METHYLANILINE 97;Benzenamine,N,2,4,6-tetramethyl-;N,2,4,6-Tetramethylaniline;N,2,4,6-Tetramethylbenzenamine
• CAS NO: 13021-14-2
• Molecular Formula: C₁₀H₁₅N
• Molecular Weight: 149.2328
• Product Categories: Amines;C9 to C10;Nitrogen Compounds
• Mol File: 13021-14-2.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 229 °C(lit.)
• Flash Point: 190 °F
• Appearance: Colorless to brown/Liquid
• Density: 0.935 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.0465mmHg at 25°C
• Refractive Index: n20/D 1.5320(lit.)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2 4 6-TRIMETHYL-N-METHYLANILINE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 2 4 6-TRIMETHYL-N-METHYLANILINE 97(13021-14-2)
• EPA Substance Registry System: 2 4 6-TRIMETHYL-N-METHYLANILINE 97(13021-14-2)

Safety Data

• Hazard Codes: Xi,N
• Statements: 36/38-50/53
• Safety Statements: 26-60-61
• RIDADR: UN 3082 9/PG 3
• WGK Germany: 3
• Hazardous Substances Data: 13021-14-2(Hazardous Substances Data)

Usage

General Description

2 4 6-Trimethyl-N-methylaniline 97 is a chemical compound that consists of three methyl groups and a methylaniline group attached to a benzene ring. It is commonly used as a stabilizing agent in the production of rubber and plastic materials. Additionally, it can also be employed as an intermediate in the synthesis of various dyes and pigments. 2 4 6-TRIMETHYL-N-METHYLANILINE 97 is known for its high purity, with a 97% concentration, which makes it a preferred choice for applications requiring precise chemical compositions and consistent performance. However, it is important to handle this chemical with care due to its potential health hazards, including skin and eye irritation, and it should only be used in well-ventilated areas with proper protective equipment.

InChI:InChI=1/C10H15N/c1-7-5-8(2)10(11-4)9(3)6-7/h5-6,11H,1-4H3

Upstream product

• 155671-06-0 2,4,6,N-tetramethyl-N-nitroso-aniline 
• 6784-26-5 2-isocyanato-1,3,5-trimethylbenzene 
• 77-78-1 dimethyl sulfate 
• 88-05-1 2,4,6-trimethylaniline 
• 13021-15-3 2,4,6-trimethyl-N,N-dimethylaniline 
• 40752-00-9 N-mesityl-N-methylacetamide 
• 25370-97-2 O-(p-toluenesulfonyl)-N-methylhydroxylamine 
• 108-67-8 1,3,5-trimethyl-benzene 
• 67-56-1 methanol 
• 65962-97-2 O-mesitylenesulfonyl-N-tert-butoxycarbonyl-N-methylhydroxylamine 

Downstream Products

• 858806-01-6 N-mesityl-N-methyl-succinamic acid 
• 102550-36-7 bis-[(2,4,6,N-tetramethyl-anilino)-methyl]-peroxide 
• 854752-54-8 3-bromo-N,2,4,6–tetramethyl aniline 
• 5279-62-9 2-(Formyl-methylamino)-1,3,5-trimethylbenzol 
• 40752-10-1 N-Methyl-N-(2,4,6-trimethyl-phenyl)-propionamide 
• 40752-11-2 N-Methyl-2-phenyl-N-(2,4,6-trimethyl-phenyl)-acetamide 
• 83070-45-5 9,10-dimethoxy-2-(2,4,6,N-tetramethyl-anilino)-6,7-dihydro-pyrimido[6,1-a]isoquinolin-4-one 
• 500730-66-5 (+/-)-N-(3-bromo-2,4,6-trimethyl-phenyl)-N-methyl-succinamic acid 
• 1290612-69-9 methyl{3-[methyl(2,4,6-trimethylphenyl)amino]-1H-isoindol-1-ylidene}(2,4,6-trimethylphenyl)ammonium perchlorate 
• 1292296-35-5 1-methyl-3-[methyl(2,4,6-trimethylphenyl)carbamoyl]-3H-imidazol-1-ium iodide 
• 1292296-58-2 methyl(2,4,6-trimethylphenyl)thiocarbamic acid (S)-1-phenyl-ethyl ester 
• 1292296-29-7 imidazole-1-carboxylic acid methyl(2,4,6-trimethylphenyl)amide 
• 1415351-71-1 S-but-3-en-2-yl mesityl(methyl)carbamothioate 
• 1616604-89-7 C₁₇H₂₁NO₃S 

Relevant articles and documents

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Synthesis of N-Alkyl Anilines from Arenes via Iron-Promoted Aromatic C-H Amination

We report both an intermolecular C-H amination of arenes to access N-methylanilines and an intramolecular variant for the synthesis of tetrahydroquinolines. A newly developed, highly electrophilic aminating reagent was key for the direct synthesis of unprotected N-methylanilines from simple arenes. The reactions display a broad functional group tolerance and employ catalytic amounts of a benign iron salt under mild reaction conditions.

SELF-IMMOLATIVE SYSTEMS

The present invention is concerned with self-immolative recognition and/or responsive systems for electrophilic compounds, especially alkylating agents, which systems may comprise disclosure or detection of the alkylating agent. The present invention is especially concerned with non-protic triggered self-immolative systems, molecules, and methods, and in particular for detection of non- protic electrophilic agents, and especially alkylating agents, for example alkyl or benzylic halides, which may be found in pesticides or fumigants, or chemical warfare agents.