• ISOPROPYLBENZYLAMINE

ISOPROPYLBENZYLAMINE

  • CasNo：4395-73-7
  • Purity：99%

Product Details;

CasNo： 4395-73-7

Molecular Formula： C10H15N

Buy High Quality High Purity ISOPROPYLBENZYLAMINE 4395-73-7 price in stock

  • Molecular Formula:C10H15N
  • Molecular Weight:149.236
  • Vapor Pressure:0.0687mmHg at 25°C 
  • Melting Point:143°C (estimate) 
  • Refractive Index:1.525 
  • Boiling Point:229.7 °C at 760 mmHg 
  • PKA:9.20±0.10(Predicted) 
  • Flash Point:97.5 °C 
  • PSA：26.02000 
  • Density:0.935 g/cm3 
  • LogP:2.96900 

ISOPROPYLBENZYLAMINE (Cas 4395-73-7) Usage

Chemical Properties

Colorless liquid
Uses Isopropylbenzylamine is primarily known for its misuse as a cutting agent for illegal drugs, particularly methamphetamine. It resembles methamphetamine structurally but does not possess the same psychoactive properties. Due to its similarity to methamphetamine, isopropylbenzylamine has been illicitly added to methamphetamine to increase its volume and weight, making it more profitable for illicit drug manufacturers and sellers.

InChI:InChI=1/C10H15N/c1-8(2)10-5-3-9(7-11)4-6-10/h3-6,8H,7,11H2,1-2H3

4395-73-7 Relevant articles

Polyazapolycyclics by condensation of aldehydes with amines. 2. Formation of 2,4,6,8,10,12-hexabenzyl-2,4,6,8,10,12-hexaazatetracyclo[5.5.0.05.9.03,11]dodecanes from glyoxal and benzylamines

Polyazapolycyclics by condensation of aldehydes with amines. 2. Formation of 2,4,6,8,10,12-hexabenzyl-2,4,6,8,10,12-hexaazatetracyclo[5.5.0.05.9.03,11]dodecanes from glyoxal and benzylamines

, J. Org. Chem. 1990, 55, 5, 1459–1466

The yield of 2c obtained from ISOPROPYLBENZYLAMINE was lower in aqueous acetonitrile than in aqueous methanol (much gummy material was produced in this reaction)...

Regioselective arene functionalization: Simple substitution of carboxylate by alkyl groups

Krueger, Tobias,Vorndran, Katja,Linker, Torsten

experimental part, p. 12082 - 12091 (2010/05/17)

Arenes with various alkyl side-chains we...

CuWO4 as a photocatalyst for room temperature aerobic ISOPROPYLBENZYLAMINE oxidation

Aaron D. Proctor,a   Shobhana Panugantia  and  Bart M. Bartlett

, Chemical Communications, Issue 9, 2018

The aerobic photochemical oxidation of benzylamine was carried out on the ternary oxides CuWO4 and BiVO4 as a test proton-coupled-electron-transfer reaction in acetonitrile. Both oxides give the coupled imine product, N-benzylidenebenzylamine, in near quantitative (98–99%) yield, with rate constants of 0.34 h−1 g−1 and 0.70 h−1 g−1 for CuWO4 and BiVO4, respectively.

4395-73-7 Process route

(4-isopropylbenzaldehyde)
122-03-2

(4-isopropylbenzaldehyde)

4-isopropylbenzylamine
4395-73-7

4-isopropylbenzylamine

cuminol
536-60-7

cuminol

Conditions
Conditions Yield
With ammonia; nickel; at 60 ℃; under 66195.7 Torr; Hydrogenation;
 
1-isopropyl-4-methylamino-2,5-cyclohexadiene-1-carboxylic acid
1202873-21-9

1-isopropyl-4-methylamino-2,5-cyclohexadiene-1-carboxylic acid

4-isopropylbenzylamine
4395-73-7

4-isopropylbenzylamine

Conditions
Conditions Yield
With chlorosulfonic acid; In dichloromethane; at 0 ℃; for 0.166667h;
76%

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