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D-Alanine Isopropyl Ester HCl

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CAS:39613-92-8
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Products Intro: Product Name:D-Alanine isopropyl ester hydrochloride
CAS:39613-92-8
Purity:99% Package:1KG,5KG,10KG
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Products Intro: Product Name:D-ALa-Oipr. HCL
CAS:39613-92-8
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG

D-Alanine Isopropyl Ester HCl manufacturers

  • D-ALa-Oipr. HCL
  • D-ALa-Oipr. HCL pictures
  • $0.00/ kg
  • 2026-04-30
  • CAS:39613-92-8
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1T+
  • Tenofovir impurity 67
  • Tenofovir impurity 67 pictures
  • $0.00 / 10mg
  • 2026-03-12
  • CAS:39613-92-8
  • Min. Order: 10mg
  • Purity: 0.98
  • Supply Ability: 5g
D-Alanine Isopropyl Ester HCl Basic information
Product Name:D-Alanine Isopropyl Ester HCl
Synonyms:D-Alanine Isopropyl Ester HCl;H-D-Ala-OiPro.HCl;H-D-Ala-OiPr·HCl;D-Alanine isopropyl ester (hydrochloride);D-Alanine 1-methylethyl ester HCl;Isopropyl (R)-2-Aminopropanoate Hydrochloride;(R)-isopropyl 2-aminopropanoate hydrochloride;propan-2-yl (2R)-2-aminopropanoate hydrochloride
CAS:39613-92-8
MF:C6H14ClNO2
MW:167.63
EINECS:
Product Categories:
Mol File:39613-92-8.mol
D-Alanine Isopropyl Ester HCl Structure
D-Alanine Isopropyl Ester HCl Chemical Properties
Melting point 80-82oC
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
color White to Off-White
Safety Information
HS Code 2922498590
MSDS Information
D-Alanine Isopropyl Ester HCl Usage And Synthesis
UsesD-Alanine Isopropyl Ester Hydrochloride is a chiral reagent used in the synthesis of nucleotide prodrugs such as (PSI-7977) for the treatment of hepatitis C. Also used in the preparation of synthetic sweeteners.
Synthesis
L-Alanine

56-41-7

Isopropyl alcohol

67-63-0

D-Alanine Isopropyl Ester HCl

39613-92-8

To a three-necked flask equipped with a mechanical stirrer, reflux condenser, thermometer and under nitrogen protection was added L-alanine (5.0 g, 56.1 mmol) and 11.1% w/w solution of isopropanol hydrochloride (73.8 g, 224.5 mmol). The reaction mixture was heated to 80-85 °C for 4 h at reflux. The reaction process was monitored by thin layer chromatography (TLC) using 7:3 ethanol-water as the unfolding agent and ninhydrin for color development. Upon completion of the reaction, the reaction mixture was concentrated under reduced pressure to remove isopropanol and the residue was co-evaporated with isopropyl acetate several times to give the final product (R)-isopropyl 2-aminopropionate hydrochloride in oil form (9.4 g, quantitative yield).

References[1] Patent: WO2016/151542, 2016, A1. Location in patent: Page/Page column 19
[2] European Journal of Organic Chemistry, 2018, vol. 2018, # 20, p. 2622 - 2628
[3] ACS Medicinal Chemistry Letters, 2016, vol. 7, # 12, p. 1197 - 1201
[4] Patent: WO2015/38596, 2015, A1. Location in patent: Page/Page column 237; 238
[5] Patent: WO2016/145142, 2016, A1. Location in patent: Page/Page column 287
D-Alanine Isopropyl Ester HCl Preparation Products And Raw materials
Raw materialsL-Alanine-->Isopropyl alcohol-->(S)-4-Methyl-2,5-oxazolidonedione
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