Basic information Uses Safety Supplier Related

ISOBUTYLAMINE HYDROCHLORIDE

Basic information Uses Safety Supplier Related

ISOBUTYLAMINE HYDROCHLORIDE Basic information

Product Name:
ISOBUTYLAMINE HYDROCHLORIDE
Synonyms:
  • 1-AMINO-2-METHYLPROPANE HYDROCHLORIDE
  • ISOBUTYLAMINE HYDROCHLORIDE
  • ISOBUTYLAMMONIUM CHLORIDE
  • isobutylamineHCl
  • 2-methylpropylazanium chloride
  • 2-Methyl-1-propanamine hydrochloride
  • IsobutylamineHydrochloride>
  • 1-Propanamine,2-methyl-, hydrochloride (9CI)
CAS:
5041-09-8
MF:
C4H12ClN
MW:
109.6
Mol File:
5041-09-8.mol
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ISOBUTYLAMINE HYDROCHLORIDE Chemical Properties

Melting point:
176.0 to 180.0 °C
storage temp. 
Inert atmosphere,Room Temperature
Water Solubility 
almost transparency in Water
form 
powder to crystal
color 
White to Almost white
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Safety Information

Hazard Codes 
Xn
Risk Statements 
36/37/38-41-37/38-22
Safety Statements 
26-36/37/39-39
HS Code 
2921199990
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ISOBUTYLAMINE HYDROCHLORIDE Usage And Synthesis

Uses

Isobutylamine hydrochloride is an organic amine hydrochloride, and it has been reported in the literature that it can be used to prepare methyl 3-(2-amino-2-thioethyl)benzoate. Methyl 3-(2-amino-2-thioethyl)benzoate is an important fine chemical raw material and pharmaceutical intermediate. It is a key intermediate for the preparation of a novel phosphate transport inhibitor, 2-[[3-[[4-(2-hydroxyethyl)-2-thiazolyl]methyl]benzoyl]amino]-5-(1-piperidinyl)-,(2E)-2-[[4-chloro-3-(trifluoromethyl)phenyl]methylene]benzoylhydrazine.

Synthesis

72-18-4

5041-09-8

The general procedure for the synthesis of isobutylamine hydrochloride from L-valine is as follows: a magnetic stirring bar, 3 mL of n-propanol (n-PrOH), 10 mmol of R-carvone and 5 mmol of L-valine were added to a pressure vessel. The vessel was heated from room temperature to 190 °C in 5 min under stirring conditions. If the reaction mixture was slurry-like, it was continued at 190°C until the solution became clear. After the vessel was cooled below the boiling point of the solvent, it was carefully vented to release the generated CO2. Subsequently, 10 mL of 2M hydrochloric acid (HCl) was added to the vessel and the vessel was again heated to 190 °C in 5 min under stirring and then cooled. The aqueous reaction mixture was washed three times with 25 mL of ether and the aqueous solvent was removed by distillation to give the hydrochloride product. The hydrochloride was transferred to a vacuum oven and dried overnight at 150 °C and 10 Torr pressure. Finally, the hydrochloride product was weighed and analyzed by infrared spectroscopy (IR) and nuclear magnetic resonance (NMR).The NMR data of 2-methylpropan-1-amine hydrochloride were as follows: δH 0.83 (6H, d, J = 4 Hz), 1.79 (1H, m, J = 8 Hz), 2.69 (2H, d, J = 8 Hz); δC 18.8, 26.2, 46.3.

References

[1] Patent: US2014/275569, 2014, A1. Location in patent: Page/Page column 0045; 0048; 0066; 0067

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