2,3-DIMETHYL-6-NITROANILINE
- Product Name
- 2,3-DIMETHYL-6-NITROANILINE
- CAS No.
- 59146-96-2
- Chemical Name
- 2,3-DIMETHYL-6-NITROANILINE
- Synonyms
- TIMTEC-BB SBB006536;6-NITRO-2,3-XYLIDINE;6-Nitro-2,3-xylidine>2,3-DIMETHYL-6-NITROANILINE;2,3-Dimethyl-6-nitroaniline,97%;2,3-DIMETHYL-6-NITROANILINE 98%;(2,3-Dimethyl-6-nitrophenyl)amine;Benzenamine, 2,3-dimethyl-6-nitro-;2,3-Dimethyl-6-nitroaniline,6-Nitro-2,3-xylidine;6-Nitro-2,3-xylidine, 2-Amino-3,4-dimethylnitrobenzene, 3-Amino-4-nitro-o-xylene
- CBNumber
- CB7334144
- Molecular Formula
- C8H10N2O2
- Formula Weight
- 166.18
- MOL File
- 59146-96-2.mol
2,3-DIMETHYL-6-NITROANILINE Property
- Melting point:
- 117-120 °C(lit.)
- Boiling point:
- 314.38°C (rough estimate)
- Density
- 1.220±0.06 g/cm3 (20 ºC 760 Torr)
- refractive index
- 1.6273 (estimate)
- storage temp.
- 2-8°C, protect from light
- form
- Crystalline Powder
- pka
- -0.16±0.25(Predicted)
- color
- Dark yellow to orange-brown
- CAS DataBase Reference
- 59146-96-2(CAS DataBase Reference)
Safety
- Hazard Codes
- Xn
- Risk Statements
- 20/21/22-36/37/38
- Safety Statements
- 26-36
- RIDADR
- 2811
- WGK Germany
- 3
- HazardClass
- 6.1
- PackingGroup
- III
- HS Code
- 29214200
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Danger
- Hazard statements
-
H302Harmful if swallowed
H312Harmful in contact with skin
H315Causes skin irritation
H319Causes serious eye irritation
H331Toxic if inhaled
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P271Use only outdoors or in a well-ventilated area.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P403+P233Store in a well-ventilated place. Keep container tightly closed.
P405Store locked up.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- N0500
- Product name
- 6-Nitro-2,3-xylidine
- Purity
- >98.0%(GC)
- Packaging
- 25g
- Price
- $62
- Updated
- 2025/07/31
- Product number
- N0500
- Product name
- 6-Nitro-2,3-xylidine
- Purity
- >98.0%(GC)
- Packaging
- 500g
- Price
- $419
- Updated
- 2025/07/31
- Product number
- D457030
- Product name
- 2,3-Dimethyl-6-nitroaniline
- Packaging
- 1g
- Price
- $55
- Updated
- 2021/12/16
- Product number
- D457030
- Product name
- 2,3-Dimethyl-6-nitroaniline
- Packaging
- 10g
- Price
- $105
- Updated
- 2021/12/16
- Product number
- X6989
- Product name
- 2,3-dimethyl-6-nitroaniline
- Packaging
- 25g
- Price
- $146
- Updated
- 2021/12/16
2,3-DIMETHYL-6-NITROANILINE Chemical Properties,Usage,Production
Chemical Properties
dark yellow to orange-brown crystalline powder
Uses
2,3-Dimethyl-6-nitroaniline is an aromatic compound used in the study of C-H pi interactions and pi-pi stacking.
Application
2,3-Dimethyl-6-nitroaniline exhibits solubility in water, ethanol, and acetone, making it a versatile reagent for diverse scientific research applications.
Synthesis
114166-32-4
138330-47-9
59146-96-2
80879-86-3
General procedure for the synthesis of 2,3-dimethyl-6-nitroaniline and 2,3-dimethyl-4-nitroaniline from the compounds (CAS:114166-32-4) and N-(2,3-dimethyl-6-nitrophenyl)acetamide: To a solution of N-(2,3-dimethyl-6-nitrophenyl)acetamide (16.0 g, 1.0 equiv.) was added a 60% H2SO4 solution (150 mL). The reaction mixture was heated to reflux temperature, maintained for 1 hour and then cooled to room temperature. The solution was diluted with ice water (100 mL) and neutralized with 2N NaOH solution. The reaction mixture was extracted with EtOAc (3 x 50 mL). The organic phases were combined, washed sequentially with saturated NaHCO3 solution (2 × 50 mL) and saturated NaCl solution (2 × 50 mL), dried over anhydrous Na2SO4 and concentrated under reduced pressure. The residue was purified by column chromatography (10% CH2Cl2/hexane) to afford 2,3-dimethyl-6-nitroaniline (5.5 g, 43%) and 2,3-dimethyl-4-nitroaniline (1.5 g, 12%). 1H NMR data for 2,3-dimethyl-6-nitroaniline (5.5 g, 43%): δ 2.05 (s, 3H), 2.20 (s, 3H), 6.15 (br s, 2H), 6.45 (d, J=8.7 Hz, 1H), 7.63 (d, J=9.0 Hz, 1H) in CDCl3; δ 2.10 (s 3H), 2.30 (s, 3H), 6.50 (d, J=8.7Hz, 1H), 7.15 (br s, 2H), 7.75 (d, J=9.0Hz, 1H). 1H NMR data for 2,3-dimethyl-4-nitroaniline: δ 2.10 (s, 3H), 2.45 (s, 3H), 4.05 (br s, 2H), 6.45 (d, J=9.0 Hz, 1H), 7.65 (d, J=8.7 Hz, 1H) in CDCl3; δ 2.00 (s, 3H), 2.35 (s 3H), 6.12 (br s, 2H), 6.53 (d, J=9.0 Hz, 1H), 7.63 (d, J=9.0 Hz, 1H).
References
[1] Patent: US6353006, 2002, B1. Location in patent: Page column 28-29
2,3-DIMETHYL-6-NITROANILINE Preparation Products And Raw materials
Raw materials
Preparation Products
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View Lastest Price from 2,3-DIMETHYL-6-NITROANILINE manufacturers
- Product
- 2,3-DIMETHYL-6-NITROANILINE 59146-96-2
- Price
- US $1.00/KG
- Min. Order
- 1g
- Purity
- 98%
- Supply Ability
- 200kgs
- Release date
- 2020-01-09