N,N-dimethyl-m-phenylenediamine

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N,N-dimethyl-m-phenylenediamine Basic information
Product Name:N,N-dimethyl-m-phenylenediamine
Synonyms:N,N-dimethylbenzene-1,3-diamine;N,N-Dimethyl-1,3-phenylenediamine;N,N-dimethyl-3-phenylenediamine;N,N-DIMETHYLMETA-PHENYLENEDIAMINE;N,N-DIMETHYL-1,3-BENZENEDIAMINE);3-Amino-N,N-dimethylaniline;m-Aminodimethylaniline;3-N,3-N-dimethylbenzene-1,3-diamine
CAS:2836-04-6
MF:C8H12N2
MW:136.19
EINECS:220-623-3
Product Categories:
Mol File:2836-04-6.mol
N,N-dimethyl-m-phenylenediamine Structure
N,N-dimethyl-m-phenylenediamine Chemical Properties
Melting point <-20 °C
Boiling point 240.49°C (rough estimate)
density 0.9950
refractive index 1.5914 (estimate)
storage temp. 2-8°C(protect from light)
pka5.11±0.10(Predicted)
AppearanceBrown to black Liquid
EPA Substance Registry System1,3-Benzenediamine, N,N-dimethyl- (2836-04-6)
Safety Information
Risk Statements 25-36/37/38-43
Safety Statements 36/37/39-45
RIDADR 2810
TSCA TSCA listed
HS Code 29215900
MSDS Information
N,N-dimethyl-m-phenylenediamine Usage And Synthesis
Chemical PropertiesLight yellow to black liquid
Synthesis
N,N-DIMETHYL-3-NITROANILINE

619-31-8

N,N-dimethyl-m-phenylenediamine

2836-04-6

Step 2: Synthesis of N1,N1-dimethylbenzene-1,3-diamine N,N-dimethyl-3-nitroaniline (1.0 g, 6.08 mmol) prepared in Step 1 was dissolved in methanol (25 mL) and 10% palladium carbon (Pd/C, 100 mg) was added. The reaction mixture was hydrogenated in a hydrogen atmosphere for 15 hours at room temperature. Upon completion of the reaction, the palladium carbon catalyst was removed by diatomaceous earth filtration and the filtrate was concentrated to dryness under reduced pressure. The resulting residue was purified by fast column chromatography (eluent: hexane/ethyl acetate=1:1, v/v) to afford N1,N1-dimethylbenzene-1,3-diamine (700 mg, yield: 90%, colorless liquid). 1H NMR (400MHz, CDCl3) δ: 7.04 (t, J=7.6Hz, 1H), 6.2 (d, J=8.0Hz, 1H), 6.11-6.08 (m, 1H), 3.60 (br s, 2H), 2.92 (s, 6H).

References[1] Journal of Organic Chemistry, 1992, vol. 57, # 19, p. 5254 - 5255
[2] Patent: EP2364983, 2011, A2. Location in patent: Page/Page column 51-52
[3] Patent: US2011/218193, 2011, A1. Location in patent: Page/Page column 42
[4] Journal fuer Praktische Chemie (Leipzig), 1986, vol. 328, # 4, p. 497 - 514
[5] Patent: WO2010/67078, 2010, A2. Location in patent: Page/Page column 79
N,N-dimethyl-m-phenylenediamine Preparation Products And Raw materials
Raw materialsN,N-Dimethyl-3-nitroaniline-->Methanol-->Hydrogen
Preparation ProductsCORIPHOSPHINE O
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