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159954-28-6

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159954-28-6 Usage

Description

6-CHLORO-3-INDOLYL-BETA-D-GALACTOPYRANOSIDE, also known as X-Gal, is a synthetic compound commonly used in molecular biology and microbiology. It is a derivative of the sugar galactose, with a chlorine atom at the 6th position and an indole group attached. X-Gal is known for its ability to produce a blue color when it interacts with specific enzymes, making it a useful tool for various applications.

Uses

Used in Molecular Biology:
6-CHLORO-3-INDOLYL-BETA-D-GALACTOPYRANOSIDE is used as a chromogenic substrate for the detection of β-galactosidase activity. This application is particularly useful in molecular cloning, where the presence of the enzyme indicates successful gene expression or the presence of a specific bacterial strain.
Used in Microbiology:
In the field of microbiology, 6-CHLORO-3-INDOLYL-BETA-D-GALACTOPYRANOSIDE is used as a selective agent for the identification of yeasts with β-glucosidase activity. This enzyme is responsible for breaking down the compound, resulting in a blue-colored product that can be easily observed and used for classification purposes.
Used in Biomedical Research:
6-CHLORO-3-INDOLYL-BETA-D-GALACTOPYRANOSIDE is also employed in biomedical research as a marker for cell differentiation, apoptosis, and other cellular processes. Its ability to produce a visible color change upon interaction with specific enzymes makes it a valuable tool for tracking and analyzing cellular events in various experimental setups.
Used in Drug Delivery Systems:
Similar to gallotannin, 6-CHLORO-3-INDOLYL-BETA-D-GALACTOPYRANOSIDE can be incorporated into drug delivery systems to improve the targeting and efficacy of therapeutic agents. Its unique properties may be utilized to enhance the delivery of drugs to specific cells or tissues, potentially improving treatment outcomes and reducing side effects.

Check Digit Verification of cas no

The CAS Registry Mumber 159954-28-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,9,5 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 159954-28:
(8*1)+(7*5)+(6*9)+(5*9)+(4*5)+(3*4)+(2*2)+(1*8)=186
186 % 10 = 6
So 159954-28-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H16ClNO6/c15-6-1-2-7-8(3-6)16-4-9(7)21-14-13(20)12(19)11(18)10(5-17)22-14/h1-4,10-14,16-20H,5H2/t10-,11-,12+,13-,14+/m1/s1

159954-28-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Chloro-3-indolyl β-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names 6-CHLORO-3-INDOLYL-β-D-GALACTOPYRANOSIDE

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:159954-28-6 SDS

159954-28-6Downstream Products

159954-28-6Relevant articles and documents

Substrate and preparation method and application thereof

-

Paragraph 0022; 0026, (2019/05/15)

The invention discloses a substrate namely alpha-D-glucoside for detecting activity of alpha-glucosidases, and further discloses a synthesis technology of the substrate. The synthesis technology comprises the steps of enabling a compound alpha-D-glucose and acetyl chloride to be subjected to a reaction, and performing purification to obtain alpha-D- pentacetylglucose; catalyzing the obtained substances with N,N-Dimethyl-1,3-diaminopropane, performing pickling, performing extraction, performing drying, and performing purifying to obtain 2,3,4,6-tetra-O-acetyl-alpha-D-acetyl-glucosamine; catalyzing the obtained substances in a dichloromethane solution, performing a reaction with trichloroacetonitrile, performing filtering, and performing purifying to obtain 2,3,4,6-tetra-O-acetyl-beta-D-glucosyl trichloroacetimidate; performing catalyzing on the obtained substances in a dichloromethane solution, performing a reaction with chromogen or fluorophore, performing extraction, merging organic phases, performing drying, performing concentrating, performing methanol redissolution, performing crystal nourishing at 4 DEG C, and performing filtering to obtain 2,3,4,6-tetra-O-acetyl-alpha-D-glucoside; and catalyzing the obtained substances in a methanolic solution, performing a reaction, then performing decoloring adsorption, performing filtering, and performing purifying. The synthesis technology of the substrate is simple and high in yield, the sensitivity of a reagent kit can be improved, the stability is good, and the specificity is high.

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