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L-Tryptophan, butyl ester, monohydrochloride is a chemical compound derived from the amino acid L-tryptophan. It is an ester formed by the reaction of L-tryptophan with butanol, and the addition of hydrochloric acid results in the formation of the monohydrochloride salt. L-Tryptophan, butyl ester, monohydrochloride is used in various applications, including pharmaceuticals and as an intermediate in the synthesis of other compounds. It is characterized by its ability to enhance the bioavailability of L-tryptophan, which is an essential amino acid involved in the production of serotonin, a neurotransmitter that contributes to mood regulation and sleep. The butyl ester form of L-tryptophan is often preferred for its improved solubility and stability, making it a valuable component in the development of medications and supplements aimed at promoting relaxation and improving sleep quality.

6330-20-7

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6330-20-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6330-20-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 6330-20:
(6*6)+(5*3)+(4*3)+(3*0)+(2*2)+(1*0)=67
67 % 10 = 7
So 6330-20-7 is a valid CAS Registry Number.

6330-20-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Butyl 2-amino-3-(1H-indol-3-yl)propanoate hydrochloride

1.2 Other means of identification

Product number -
Other names L-Tryptophan,butyl ester,monohydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6330-20-7 SDS

6330-20-7Relevant academic research and scientific papers

Solvent free three-component synthesis of 2,4,5-trisubstituted-1H-pyrrol-3-ol-type Compounds from L-tryptophan: DFT-B3LYP calculations for the reaction mechanism and 3H-pyrrol-3-one?1H-pyrrol-3-ol tautomeric equilibrium

Becerra, Lili Dahiana,Coy-Barrera, Ericsson,Quiroga, Diego

, (2020/10/12)

In this paper, we describe the solvent-free three-component synthesis of 2,4,5-trisubstituted-1H-pyrrol-3-ol-type compounds from L-tryptophan. The first step of the synthetic methodology involved the esterification of L-tryptophan in excellent yields (93–98%). Equimolar mixtures of alkyl 2-aminoesters, 1,3-dicarbonyl compounds, and potassium hydroxide (0.1 eq.) were heated under solvent-free conditions. The title compounds were obtained in moderate to good yields (45%–81%). Density functional theory using “Becke, 3-parameter, Lee–Yang–Parr” correlational functional (DFT-B3LYP) calculations were performed to understand the molecular stability of the synthesized compounds and the tautomeric equilibrium from 3H-pyrrol-3-one type intermediates to 1H-pyrrol-3-ol type aromatized rings.

Preparation method of tryptophan ester hydrochloride

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Paragraph 0053-0056, (2019/12/02)

The invention discloses a preparation method of tryptophan ester hydrochloride. The preparation method comprises the following steps: 1) reacting p-toluenesulfonyl chloride with tryptophan in alcoholto obtain a tryptophan ester hydrochloride crude product; and 2) purifying the crude product to obtain the tryptophan ester hydrochloride. According to the method, the p-toluenesulfonyl chloride and the lower alcohol which are available in the market and low in price are used as raw materials, reaction conditions are easy to implement, operation is easy, the cost is greatly reduced compared with other methods, the obtained product is high in purity and the method is suitable for large-scale industrial production.

COMPOSITIONS AND METHODS FOR CYCLOFRUCTANS AS SEPARATION AGENTS

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Page/Page column 45-49; 59, (2010/12/31)

The present invention relates to derivatized cyclofructan compounds, compositions comprising derivatized cyclofructan compounds, and methods of using compositions comprising derivatized cyclofructan compounds for chromatographic separations of chemical species, including enantiomers. Said compositions may comprise a solid support and/or polymers comprising derivatized cyclofructan compounds.

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