| Identification | More | [Name]
Ethyl L-tryptophanate hydrochloride | [CAS]
2899-28-7 | [Synonyms]
ETHYL 2-AMINO-3-(1H-INDOL-3-YL)PROPANOATE, HYDROCHLORIDE
H-TRP-OET HCL
L-2-AMINO-3-INDOLYLPROPANOIC ACID ETHYL ESTER HYDROCHLORIDE
L-A-AMINO-3-INDOLEPROPIONIC ACID ETHYL ESTER HYDROCHLORIDE
L-B-3-INDOLYLALANINE ETHER ESTER HYDROCHLORIDE
L-TRYPTOPHAL ETHYL ESTER HCL
L-TRYPTOPHAN ETHYL ESTER HYDROCHLORIDE
L-TRYPTOPHAN ETHYL ESTER HYDROCHLORIDE SALT
TRYPTOPHAN-OET HCL
L-Tryptophan Ethyl Ester HCl
ethyl L-tryptophanate monohydrochloride
L-TRYPTOPHAN ETHYL ESTER
L-TRYPTOPHAN ETHYL ESTER HYDROCHLORIDE 99%
L-TRYPTOPHAN MTHYLESTER HYDROCHLORIDE
(S)-TRYPTOPHAN ETHYL ESTER HYDROCHLORIDE
Ethyl L-tryptophanate hydrochloride
H-L-Trp-OEt*HCl
L-Tryptophane ethyl ester hydrochloride | [EINECS(EC#)]
220-786-0 | [Molecular Formula]
C13H17ClN2O2 | [MDL Number]
MFCD00038993 | [Molecular Weight]
268.74 | [MOL File]
2899-28-7.mol |
| Chemical Properties | Back Directory | [Appearance]
Light grey crystalline powder | [Melting point ]
220-225 °C (dec.) | [alpha ]
10 º (c=2% in H2O) | [storage temp. ]
0-6°C | [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
Powder | [pka]
pKa 7.10±0.05(H2O t=25.0±0.1 I=0.1(NaCl) N2atmosphere) (Uncertain);10.79±0.02 (H2O t=25.0±0.1 I=0.1(NaCl) N2atmosphere) (Uncertain) | [color ]
White to off-white | [Optical Rotation]
[α]20/D +10±1°, c =2% in H2O | [InChI]
InChI=1/C13H16N2O2.ClH/c1-2-17-13(16)11(14)7-9-8-15-12-6-4-3-5-10(9)12;/h3-6,8,11,15H,2,7,14H2,1H3;1H/t11-;/s3 | [InChIKey]
PESYCVVSLYSXAK-XAAIUDFWNA-N | [SMILES]
C12C=CC=CC=1NC=C2C[C@H](N)C(=O)OCC.Cl |&1:10,r| | [CAS DataBase Reference]
2899-28-7(CAS DataBase Reference) |
| Safety Data | Back Directory | [Safety Statements ]
S22:Do not breathe dust .
S24/25:Avoid contact with skin and eyes . | [WGK Germany ]
3
| [HS Code ]
29339900 |
| Hazard Information | Back Directory | [Chemical Properties]
Light grey crystalline powder | [Uses]
These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements. | [reaction suitability]
reaction type: solution phase peptide synthesis | [Synthesis]
Preparation of Example 110 Ethyl L-tryptophan hydrochloride: L-tryptophan (14.3 g, 0.07 mol) was dissolved in 200 ml of ethanol containing about 7 g of anhydrous hydrogen chloride and the reaction was carried out at reflux for 5 hours. After completion of the reaction, the mixture was cooled and the precipitated solid was purified by recrystallization from a solvent mixture of ethanol/ether. The product was obtained as 17.4 g in 92.5% yield, melting point not provided. The product was chemically named L-2-amino-3-indolepropionic acid ethyl ester hydrochloride. | [References]
[1] Patent: US4824850, 1989, A |
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