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Ethyl 2-aminopropanoate hydrochloride

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Ethyl 2-aminopropanoate hydrochloride Basic information

Product Name:
Ethyl 2-aminopropanoate hydrochloride
Synonyms:
  • (DL-Alanina ethyl ester hydrochloride
  • ETHYL 2-AMINOPROPANOATE HCl
  • DL-Alanine ethyl ester hydrochloride≥ 99% (Assay)
  • l 2-aminopropanoate hydrochloride
  • DL-Ala-OEt·HCl
  • Methisosildenafil Impurity 7
  • Alanine, ethyl ester,hydrochloride (1:1)
  • [(2R)-1-ethoxy-1-oxopropan-2-yl]ammonium
CAS:
617-27-6
MF:
C5H12ClNO2
MW:
153.61
EINECS:
210-507-0
Product Categories:
  • Alanine [Ala, A]
  • Amino Acids 13C, 2H, 15N
  • Amino Acids & Derivatives
  • Inhibitors
  • Alanine
  • Amino Acid Derivatives
  • Peptide Synthesis
  • bc0001
Mol File:
617-27-6.mol
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Ethyl 2-aminopropanoate hydrochloride Chemical Properties

Melting point:
85-87 °C(lit.)
storage temp. 
Inert atmosphere,2-8°C
solubility 
Methanol (Sparingly), Water
form 
Granular Powder and Granules
color 
White
Sensitive 
Hygroscopic
BRN 
3654425
InChI
InChI=1S/C5H11NO2.ClH/c1-3-8-5(7)4(2)6;/h4H,3,6H2,1-2H3;1H
InChIKey
JCXLZWMDXJFOOI-UHFFFAOYSA-N
SMILES
C(=O)(C(N)C)OCC.Cl
CAS DataBase Reference
617-27-6(CAS DataBase Reference)
EPA Substance Registry System
Alanine, ethyl ester, hydrochloride (617-27-6)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
22-24/25
WGK Germany 
3
TSCA 
Yes
HS Code 
29224999

MSDS

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Ethyl 2-aminopropanoate hydrochloride Usage And Synthesis

Chemical Properties

White Crystalline Solid

Uses

Alanine derivative

reaction suitability

reaction type: solution phase peptide synthesis

Synthesis

64-17-5

302-72-7

617-27-6

The general procedure for the synthesis of ethyl 2-aminopropionate hydrochloride from ethanol and DL-alanine was as follows: commercially available DL-alanine (5.00 g, 56.12 mmol) was dissolved in 150 mL of anhydrous ethanol, 5 mL of 37% concentrated hydrochloric acid was added, and the mixture was refluxed for 5 hours. After completion of the reaction, the solvent was removed by evaporation and the resulting colorless oily residue was vacuum dried to give the target product in 92% yield. The product was characterized by 1H NMR (CDCl3): δ 1.05 (t, 3H, J=7.07Hz, -OCH2CH3), 1.45 (d, 3H, J=7.25Hz, -CHCH3), 3.48 (q, 2H, J=7.07Hz, -OCH2CH3), and 4.02 ppm (q, 1H, J=7.25Hz, - CHCH3). High-resolution mass spectrometry (HRMS, ESI, 140 eV) analysis showed that the m/z [M+H+] calculated value for C5H12NO2 was 118.0868 and the measured value was 118.0794.

References

[1] Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1994, # 7, p. 1455 - 1462
[2] Dalton Transactions, 2008, # 13, p. 1689 - 1697
[3] Polyhedron, 2014, vol. 67, p. 520 - 528
[4] Scientia Pharmaceutica, 2001, vol. 69, # 4, p. 329 - 350
[5] Bioorganic and Medicinal Chemistry, 2009, vol. 17, # 6, p. 2336 - 2350

Ethyl 2-aminopropanoate hydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

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