Ethyl L-tryptophanate hydrochloride
Ethyl L-tryptophanate hydrochloride Basic information
- Product Name:
- Ethyl L-tryptophanate hydrochloride
- 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
- H-TRP-OET·HCL
- L-Tryptophan Ethyl Ester HCl
- ethyl L-tryptophanate monohydrochloride
- CAS:
- 2899-28-7
- MF:
- C13H17ClN2O2
- MW:
- 268.74
- EINECS:
- 220-786-0
- Product Categories:
-
- Amino Acids and Derivatives
- Amino hydrochloride
- Amino Acid Derivatives
- Peptide Synthesis
- Tryptophan
- Amino Acids
- Mol File:
- 2899-28-7.mol
Ethyl L-tryptophanate hydrochloride Chemical Properties
- Melting point:
- 220-225 °C (dec.)
- alpha
- 10 º (c=2% in H2O)
- storage temp.
- Keep in dark place,Sealed in dry,Room Temperature
- 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 activity
- [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 Information
- Safety Statements
- 22-24/25
- WGK Germany
- 3
- HS Code
- 29339900
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
Ethyl L-tryptophanate hydrochloride Usage And Synthesis
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
73-22-3
2899-28-7
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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Ethyl L-tryptophanate hydrochloride(2899-28-7)Related Product Information
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- L-TRYPTOPHAN BENZYL ESTER 98
- N-[(tert-Butoxy)carbonyl]-D-tryptophan
- 3-Indolepropionic acid
- TRYPTAMINE HYDROCHLORIDE
- H-TRP-OTBU HCL