93690
L-Tryptophan ethyl ester hydrochloride
≥99.0% (AT)
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About This Item
Empirical Formula (Hill Notation):
C13H16N2O2 · HCl
CAS Number:
Molecular Weight:
268.74
UNSPSC Code:
12352209
NACRES:
NA.22
PubChem Substance ID:
EC Number:
220-786-0
Beilstein/REAXYS Number:
3919010
MDL number:
Quality Level
assay
≥99.0% (AT)
form
powder
optical activity
[α]20/D +10±1°, c = 2% in H2O
reaction suitability
reaction type: solution phase peptide synthesis
mp
220-225 °C (dec.)
application(s)
peptide synthesis
SMILES string
Cl.CCOC(=O)[C@@H](N)Cc1c[nH]c2ccccc12
InChI
1S/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-;/m0./s1
InChI key
PESYCVVSLYSXAK-MERQFXBCSA-N
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Kento Takayama et al.
Journal of natural medicines, 75(1), 116-128 (2020-10-21)
Indole is produced from dietary tryptophan by tryptophanase in intestinal bacteria, such as Escherichia coli. In the liver, indole is converted into indoxyl sulfate, a uremic toxin and risk factor for chronic kidney disease (CKD). Probiotics and prebiotics are currently
Diana E Schlamadinger et al.
The journal of physical chemistry. B, 113(44), 14769-14778 (2009-10-13)
Ultraviolet resonance Raman (UVRR) spectra of tryptophan compounds in various solvents and a model peptide are presented and reveal systematic changes that reflect solvent polarity, hydrogen bond strength, and cation-pi interaction. The commonly utilized UVRR spectral marker for environment polarity
V Iu Shviadas et al.
Biokhimiia (Moscow, Russia), 45(4), 629-635 (1980-04-01)
The hydrolysis of L-tryptophane ethyl ester catalyzed by alpha-chymotrypsin and the effect of ethyl ster of D-tryptophane on the course of the reaction were studied. A kinetic pattern of a three-step enzymatic reaction based on the assumption that the enzyme
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 93690-5G | 04061832643137 |