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3-CHLORO-N-METHYLBENZYLAMINE

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Products Intro: Product Name:3-CHLORO-N-METHYLBENZYLAMINE
CAS:39191-07-6
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-65962
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:3-chloro-n-methylbenzylamine
CAS:39191-07-6
Purity:0.99 Package:1kg
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Products Intro: Product Name:3-CHLORO-N-METHYLBENZYLAMINE
CAS:39191-07-6
Purity:99% Package:1KG;1USD
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Products Intro: Product Name:N-(3-chlorobenzyl)-N-methylamine
CAS:39191-07-6

3-CHLORO-N-METHYLBENZYLAMINE manufacturers

3-CHLORO-N-METHYLBENZYLAMINE Basic information
Product Name:3-CHLORO-N-METHYLBENZYLAMINE
Synonyms:3-CHLORO-N-METHYLBENZYLAMINE;M-CHLORO-N-METHYLBENZYLAMINE;3-Chloro-N-methylbenzenemethanamine;N-Methyl-3-chlorobenzylamine;N-(3-CHLOROBENZYL)-N-METHYLAMINE;1-(3-Chlorophenyl)-N-MethylMethanaMine;3-Chloro-N-methylbenzylamine ,97%;3-CHLORO-N-METHYLBEN
CAS:39191-07-6
MF:C8H10ClN
MW:155.62
EINECS:254-343-8
Product Categories:Polyamines;Amines;C8;Nitrogen Compounds
Mol File:39191-07-6.mol
3-CHLORO-N-METHYLBENZYLAMINE Structure
3-CHLORO-N-METHYLBENZYLAMINE Chemical Properties
Boiling point 97 °C/0.6 mmHg (lit.)
density 1.072 g/mL at 25 °C (lit.)
refractive index n20/D 1.5395(lit.)
Fp 115 °F
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka9.34±0.10(Predicted)
AppearanceColorless to light yellow Liquid
Sensitive Air Sensitive
InChI1S/C8H10ClN/c1-10-6-7-3-2-4-8(9)5-7/h2-5,10H,6H2,1H3
InChIKeyZPNLAQVYPIAHTO-UHFFFAOYSA-N
SMILESCNCc1cccc(Cl)c1
NIST Chemistry ReferenceN-methyl-m-chlorobenzylamine(39191-07-6)
EPA Substance Registry SystemBenzenemethanamine, 3-chloro-N-methyl- (39191-07-6)
Safety Information
Hazard Codes Xn
Risk Statements 10-22-38-41
Safety Statements 16-26-36/37/39
RIDADR UN 1993 3/PG 1
WGK Germany 2
TSCA TSCA listed
HazardClass 3
PackingGroup 
HS Code 29214990
Storage Class3 - Flammable liquids
Hazard ClassificationsAcute Tox. 4 Oral
Aquatic Chronic 3
Eye Dam. 1
Flam. Liq. 3
Skin Irrit. 2
MSDS Information
ProviderLanguage
SigmaAldrich English
3-CHLORO-N-METHYLBENZYLAMINE Usage And Synthesis
Synthesis
4-Chlorobenzyl chloride

104-83-6

Methylamine

74-89-5

3-CHLORO-N-METHYLBENZYLAMINE

39191-07-6

GENERAL STEPS: An ethanol solution of methylamine (33% w/v, 17 mL) was slowly added dropwise to 4-chlorobenzyl chloride (2.0 g, 12.42 mmol), followed by heating the reaction mixture to reflux overnight. Upon completion of the reaction, ethanol was removed by distillation under reduced pressure by rotary evaporator. The residue was diluted with deionized water (100 mL) and washed with ethyl acetate (150 mL × 2). The aqueous phase was adjusted to pH 8 with solid potassium carbonate and then extracted with ethyl acetate (100 mL × 2). All organic phases were combined, washed with deionized water (100 mL), dried over anhydrous sodium sulfate, and finally the target product, N-methyl-3-chlorobenzylamine (1.7 g), was obtained by concentration under reduced pressure. The product was characterized by 1H NMR (300 MHz, DMSO-d6): δ 2.22 (s, 3H), 3.32 (br s, 1H), 3.62 (s, 2H), 7.25-7.38 (m, 4H); ESI-MS (m/z) 156 (M + H).

References[1] Patent: WO2017/199103, 2017, A1. Location in patent: Page/Page column 28
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