Name | DL-Ethyl 2-aminopropanoate hydrochloride |
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Synonyms |
Ethyl (S)-2-Aminopropionate Hydrochloride
L-Alanine Ethyl Ester Hydrochloride Ethyl alaninate hydrochloride (1:1) (S)-2-Aminopropionic Acid Ethyl Ester Hydrochloride EINECS 210-507-0 MFCD00013018 Ethyl L-alaninate hydrochloride DL-ethyl 2-aminopropanoate hydrochloride Alanine, ethyl ester, hydrochloride (1:1) 1-Ethoxy-1-oxopropan-2-aminium chloride ethyl 2-aminopropanoate,hydrochloride H-Ala-OEt·HCl L-Ethyl 2-aminopropanoate hydrochloride H-DL-Ala-OEt·HCl Ethyl 2-aminopropanoate hydrochloride |
Description | H-DL-Ala-OEt.HCl is an alanine derivative[1]. |
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Related Catalog | |
In Vitro | Amino acids and amino acid derivatives have been commercially used as ergogenic supplements. They influence the secretion of anabolic hormones, supply of fuel during exercise, mental performance during stress related tasks and prevent exercise induced muscle damage. They are recognized to be beneficial as ergogenic dietary substances[1]. |
References |
Density | 0.821 g/cm3 |
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Boiling Point | 127.8ºC at 760 mmHg |
Melting Point | 85-87 °C(lit.) |
Molecular Formula | C5H12ClNO2 |
Molecular Weight | 153.607 |
Flash Point | 3.5ºC |
Exact Mass | 153.055649 |
PSA | 52.32000 |
LogP | 1.39900 |
Storage condition | 2-8°C |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
Risk Phrases | R36/37/38 |
Safety Phrases | S22-S24/25 |
RIDADR | NONH for all modes of transport |
WGK Germany | 3 |
Packaging Group | I; II; III |
~95% 617-27-6 |
Literature: Weber, Edwin; Reutel, Christiane; Foces-Foces, Concepcion; Llamas-Saiz, Antonio L. Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1994 , # 7 p. 1455 - 1462 |
~88% 617-27-6 |
Literature: Stauffer Chemical Company Patent: US4361439 A1, 1982 ; |
~62% 617-27-6 |
Literature: Zwierzak, Andrzej; Pilichowska, Slawomira Synthesis, 1982 , # 11 p. 922 - 924 |
~% 617-27-6 |
Literature: Synthesis, , # 2 p. 202 - 204 |
~% 617-27-6 |
Literature: Synthesis, , # 2 p. 202 - 204 |
~% 617-27-6 |
Literature: Hoppe-Seyler's Zeitschrift fuer Physiologische Chemie, , vol. 283, p. 73 |
~% 617-27-6 |
Literature: Chemische Berichte, , vol. 54, p. 1436 |
Precursor 8 | |
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DownStream 10 | |