3-Methyl-4-nitroaniline
3-Methyl-4-nitroaniline Basic information
- Product Name:
- 3-Methyl-4-nitroaniline
- Synonyms:
-
- 3-METHYL-4-NITRO-PHENYLAMINE
- 3-METHYL-4-NITROBENZENEAMINE
- 3-METHYL-4-NITROANILINE
- 3-Amino-6-nitrotoluene
- 5-AMINO-2-NITROTOLUENE
- 4-AMINO-3-METHYL-4-NITROBENZENE
- 4-NITRO-M-TOLUIDINE
- 4-nitro-3-methylaniline
- CAS:
- 611-05-2
- MF:
- C7H8N2O2
- MW:
- 152.15
- EINECS:
- 210-247-8
- Product Categories:
-
- Aromatics Compounds
- Functional Materials
- Organic Nonlinear Optical Materials
- Aromatics
- Mol File:
- 611-05-2.mol
3-Methyl-4-nitroaniline Chemical Properties
- Melting point:
- 136-137°C
- Boiling point:
- 330.0±22.0 °C(Predicted)
- Density
- 1.269±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- solubility
- Methanol
- form
- Solid
- pka
- 1.12±0.10(Predicted)
- color
- Brown Crystalline
- BRN
- 2209112
- CAS DataBase Reference
- 611-05-2(CAS DataBase Reference)
Safety Information
- Hazard Codes
- T
- Risk Statements
- 23/24/25-33-51/53
- Safety Statements
- 28-36/37-45-61
- RIDADR
- 2660
- HazardClass
- 6.1
- PackingGroup
- III
- HS Code
- 2921420090
MSDS
- Language:English Provider:3-Amino-6-nitrotoluene
- Language:English Provider:ALFA
3-Methyl-4-nitroaniline Usage And Synthesis
Chemical Properties
Brown Crystalline Solid
Uses
3-Methyl-4-nitrobenzeneamine (cas# 611-05-2) is a compound useful in organic synthesis.
Synthesis Reference(s)
Synthetic Communications, 18, p. 2161, 1988 DOI: 10.1080/00397918808068287
Synthesis
99584-85-7
611-05-2
General procedure for the synthesis of 3-methyl-4-nitroaniline (20-2) from 3-methyl-4-nitrobenzamide (20-1, 40 g, 222 mmol): 20-1 was dissolved in 400 mL of methanol/water (v/v=1/1) mixed solvent and cooled to 0 °C. Subsequently, sodium hydroxide (35.6 g, 888 mmol) was added to the solution and stirred for 0.5 hours. Sodium hypochlorite solution (380 g, 556 mmol) was added slowly and dropwise at 0°C. The reaction mixture was gradually warmed up to room temperature (20°C) and stirring was continued for 18 hours. After that, the mixture was further warmed up to 35°C and stirred for 1 hour, then warmed up to 75°C and stirred for 0.5 hours. After completion of the reaction, the mixture was cooled to room temperature. The pH was adjusted to 6.0 with hydrochloric acid, at which time a brown precipitate was produced. The precipitate was collected by filtration and washed twice with 200 mL of water to give the final 20-2 (29 g, 86% yield) as a tan powder.
References
[1] Patent: US9138427, 2015, B2. Location in patent: Page/Page column 297
3-Methyl-4-nitroanilineSupplier
- Tel
- 18210857532; 18210857532
- jkinfo@jkchemical.com
- Tel
- 4006356688 18621169109
- market03@meryer.com
- Tel
- 821-50328103-801 18930552037
- 3bsc@sina.com
- Tel
- 400-6106006
- saleschina@alfa-asia.com
- Tel
- 021-67121386
- Sales-CN@TCIchemicals.com
3-Methyl-4-nitroaniline(611-05-2)Related Product Information
- Methylparaben
- Kresoxim-methyl
- 4-Nitrotoluene
- m-Toluidine
- Bensulfuron methyl
- 3,3',5,5'-Tetramethylbenzidine dihydrochloride
- 4'-Nitroacetanilide
- N,N-Dimethylaniline
- N-Methylaniline
- METHYL THIOPHENE-2-CARBOXYLATE
- 6-Aminocaproic acid
- Methyl acetate
- Methyl acrylate
- ALTRENOGEST
- Glycine
- Thiophanate-methyl
- Tris(hydroxymethyl)aminomethane
- 3-Aminophenol