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Ethyl L-valinate hydrochloride

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Ethyl L-valinate hydrochloride Basic information

Product Name:
Ethyl L-valinate hydrochloride
Synonyms:
  • H-VAL-OET HCL
  • H-VAL-OET HYDROCHLORIDE
  • (L)-ETHYL 2-AMINO-3-METHYLBUTANOATE HYDROCHLORIDE
  • ETHYL 2-AMINO-3-METHYLBUTANOATE HYDROCHLORIDE
  • L-VALINE ETHYL ESTER HCL
  • L-VALINE ETHYL ESTER HYDROCHLORIDE
  • VALINE-OET HCL
  • H-VAL-OET·HCL
CAS:
17609-47-1
MF:
C7H16ClNO2
MW:
181.66
EINECS:
241-580-7
Product Categories:
  • Valine [Val, V]
  • Amino hydrochloride
  • Amino Acid Derivatives
  • Peptide Synthesis
  • Valine
  • Amino Acids
  • Amino Acid Derivatives
Mol File:
17609-47-1.mol
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Ethyl L-valinate hydrochloride Chemical Properties

Melting point:
102-105 °C(lit.)
alpha 
7 º (c=2, H2O)
storage temp. 
Sealed in dry,Room Temperature
Water Solubility 
Soluble in water
solubility 
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form 
powder to crystal
color 
White to Almost white
optical activity
[α]20/D +6.7°, c = 2 in H2O
InChI
InChI=1/C7H15NO2.ClH/c1-4-10-7(9)6(8)5(2)3;/h5-6H,4,8H2,1-3H3;1H/t6-;/s3
InChIKey
PQGVTLQEKCJXKF-RGMNGODLSA-N
SMILES
[C@H](N)(C(C)C)C(=O)OCC.Cl |&1:0,r|
CAS DataBase Reference
17609-47-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Safety Statements 
24/25
WGK Germany 
3
HS Code 
29224999

MSDS

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Ethyl L-valinate hydrochloride Usage And Synthesis

Chemical Properties

white crystalline powder

Uses

peptide synthesis

reaction suitability

reaction type: solution phase peptide synthesis

Synthesis

64-17-5

72-18-4

17609-47-1

The general procedure for the synthesis of L-valine ethyl ester hydrochloride from ethanol and L-valine is as follows: 5 kg (42.7 mol) of L-valine and 4 kg of anhydrous ethanol were added to a 50-liter glass reactor and stirred until complete dissolution. After cooling the reaction mixture to 0-10°C, 8.8 liters of thionyl chloride were added slowly and dropwise. After the dropwise addition was completed, the reaction mixture was gradually heated to reflux and the reaction was maintained for 18 hours. Upon completion of the reaction, the reaction solution was concentrated to dryness. Subsequently, 15 liters of isopropyl acetate was added to the dried residue at 15 to 20°C and stirred for 1 hour. Finally, the product was collected by diafiltration to give 6.1 kg of off-white solid, Intermediate 1 (where R1 is ethyl).

References

[1] Tetrahedron, 2005, vol. 61, # 35, p. 8423 - 8442
[2] Journal of the Indian Chemical Society, 2001, vol. 78, # 3, p. 137 - 141
[3] Journal of the American Chemical Society, 2018, vol. 140, # 22, p. 6818 - 6822
[4] Chemistry of Natural Compounds, 1994, vol. 30, # 2, p. 238 - 244
[5] Khimiya Prirodnykh Soedinenii, 1994, # 2, p. 261 - 268

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