5-Bromo-4-chloro-3-indolyl-beta-D-glucoside

Product Name: 5-Bromo-4-chloro-3-indolyl-beta-D-glucoside
CAS No.: 15548-60-4
Chemical Name: 5-Bromo-4-chloro-3-indolyl-beta-D-glucoside
Synonyms: X-GLC;X-GLU;GLUC(X-);X-GLUCOSIDE;X-BETA-D-GLC;X-BETA-D-GLUCOSIDE;X-Glc, X-glucoside;X-Gluc(5-Bromo-4-Chloro-3-Indolyl-;5-bromo-4-chloro-3-indoxylglucoside;5-Bromo-4-chloroindolylglucopyranoside
CBNumber: CB0683827
Molecular Formula: C14H15BrClNO6
Formula Weight: 408.63
MOL File: 15548-60-4.mol

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5-Bromo-4-chloro-3-indolyl-beta-D-glucoside Property

Melting point:: 249-251 °C
alpha: -81 º (c=1, DMF)
Boiling point:: 673.9±55.0 °C(Predicted)
Density: 1.882±0.06 g/cm3(Predicted)
storage temp.: −20°C
solubility: DMF: 50 mg/mL, clear, colorless to very faintly yellow
pka: 12.74±0.70(Predicted)
form: Crystalline powder
color: White to Light yellow
BRN: 1552603
InChI: InChI=1/C14H15BrClNO6/c15-5-1-2-6-9(10(5)16)7(3-17-6)22-14-13(21)12(20)11(19)8(4-18)23-14/h1-3,8,11-14,17-21H,4H2/t8-,11-,12+,13-,14-/s3
InChIKey: OPIFSICVWOWJMJ-OTXFOCTGSA-N
SMILES: C12C(Cl)=C(C=CC=1NC=C2O[C@H]1[C@H](O)[C@H]([C@H](O)[C@@H](CO)O1)O)Br |&1:11,12,14,15,17,r|
CAS DataBase Reference: 15548-60-4(CAS DataBase Reference)

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Safety

Safety Statements: 24/25
WGK Germany: 3
F: 8-10-21
HS Code: 29389090
Storage Class: 11 - Combustible Solids

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P330Rinse mouth.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

P403+P233Store in a well-ventilated place. Keep container tightly closed.

P405Store locked up.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: B4527
Product name: 5-Bromo-4-chloro-3-indolyl β-D-glucopyranoside
Purity: ≥97%
Packaging: 5mg
Price: $170
Updated: 2026/03/19

Sigma-Aldrich

Product number: B4527
Product name: 5-Bromo-4-chloro-3-indolyl β-D-glucopyranoside
Purity: ≥97%
Packaging: 25mg
Price: $553
Updated: 2026/03/19

TCI Chemical

Product number: B5393
Product name: 5-Bromo-4-chloro-3-indolyl β-D-Glucopyranoside [for Biochemical Research]
Purity: >98.0%(HPLC)
Packaging: 200mg
Price: $36
Updated: 2026/03/19

TCI Chemical

Product number: B5393
Product name: 5-Bromo-4-chloro-3-indolyl β-D-Glucopyranoside [for Biochemical Research]
Purity: >98.0%(HPLC)
Packaging: 1g
Price: $100
Updated: 2026/03/19

Sigma-Aldrich

Product number: B4527
Product name: 5-Bromo-4-chloro-3-indolyl β-D-glucopyranoside
Purity: ≥97%
Packaging: 100mg
Price: $1710
Updated: 2026/03/19

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5-Bromo-4-chloro-3-indolyl-beta-D-glucoside Chemical Properties,Usage,Production

Chemical Properties

white to off-white powder

Uses

Substrate for beta-D-glucosidase

Definition

ChEBI: An indolyl carbohydrate that is the beta-D-glucoside of 3-hydroxy-1H-indole in which the indole moiety is substituted at positions 4 and 5 by chlorine and bromine, respectively. It is used to test for th presence of an enzyme, beta-glucosidase, which cleaves the glycosidic bond to give 5-bromo-4-chloro-3-hydroxy-1H-indole, which immediately dimerises to give an intensely blue product.

Synthesis

Method 1: Take 5-bromo-4-chloro-3-indolyl-2,3,4,6-tetra-O-acetyl--D-glucopyranoside dissolved in 15mL of methanol and cooled to 0 in an ice bath; then add 3mL (0.5 mol/L) of sodium methanol methanol solution dropwise and stirred for 5h at this temperature; at the end of the reaction, the reaction solution was poured into pre-treated cationic exchange resin (cationic). After the reaction, the reaction solution was poured into the pre-treated cation exchange resin (pretreatment method of the resin: firstly, rinse the resin with water; then soak it in 5% hydrochloric acid for about 4h, and wash it to neutral; then soak it in 5% sodium hydroxide solution for about 4h, and wash it to neutral; finally, soak it in 5% hydrochloric acid for 4h, and wash it to neutral), and then it was slowly stirred for 5-10min, and then filtered, and then rinsed by methanol, and then the filtrate was evaporated and removed the solvent, and it was obtained as 0.49g of white solid 5-bromo-4-chloro-3-beta-indolyl-beta-indoline-3-beta-indole. -indolyl-beta-D-glucopyranoside, yield 81.6%, melting point 86.5 .

Method 2: 40 mg of compound 5 was dissolved in 5 mL of methanol, cooled to 0 C in an ice bath, then 5 mL (0.2 mol/L) of methanol solution of sodium methanol was added dropwise and stirred for 3 h at this temperature; at the end of the reaction, the reaction solution was poured into pre-treated cation-exchange resin (pre-treatment method as in section 1.2.1) and stirred slowly for 5~10 min; filtered, rinsed with methanol, the filtrate was evaporated to remove the solvent to obtain 10mg of white solid, i.e., 5-bromo-4-chloro-3-indolyl-beta-D-glucopyranoside, with a yield of 40.3% and a melting point of 82.1C. The reaction was completed by pouring the reaction solution into the pre-treated cation exchange resin (pretreatment method as in section 1.2.1).

5-Bromo-4-chloro-3-indolyl-beta-D-glucoside Preparation Products And Raw materials

Raw materials

Preparation Products

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5-Bromo-4-chloro-3-indolyl-beta-D-glucoside Suppliers

Americas 1 Belgium 1 Canada 2 China 119 Europe 4 France 2 Germany 4 India 9 Italy 1 Japan 2 Switzerland 3 United Kingdom 12 United States 21 Global 181

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View Lastest Price from 5-Bromo-4-chloro-3-indolyl-beta-D-glucoside manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD

Product: 5-Bromo-4-chloro-3-indolyl-beta-D-glucoside 15548-60-4
Price: US $0.00-0.00/KG
Min. Order: 1KG
Purity: 99%
Supply Ability: 3500kg/month
Release date: 2026-01-27

Zhuozhou Wenxi import and Export Co., Ltd

Product: 5-Bromo-4-chloro-3-indolyl-beta-D-glucoside 15548-60-4
Price: US $15.00-10.00/KG
Min. Order: 1KG
Purity: 99%+ HPLC
Supply Ability: Monthly supply of 1 ton
Release date: 2021-08-11

Career Henan Chemical Co

Product: 5-Bromo-4-chloro-3-indolyl-beta-D-glucoside 15548-60-4
Price: US $1.00/kg
Min. Order: 1kg
Purity: 98%
Supply Ability: 100KG
Release date: 2018-12-17

15548-60-4, 5-Bromo-4-chloro-3-indolyl-beta-D-glucosideRelated Search:

Ascorbyl glucoside Indometacin Indole-3-acetic acid Tetrahydro-4H-pyran-4-one Tetrahydropyran Decyl glucoside 2-acetamido-2-deoxy-4-O-A-L-*fucopyranosyl-D-gluc Difluorochloromethane 4,6-diamino-2-hydroxy-1,3-cyclohexane3,6’diamino-3,6’-dideoxydi-alpha-d-glu Podophyllotoxin (6-Chloro-3-indolyl)-β-D-glucuronide cyclohexylammonium salt 2-acetamido-2-deoxy-6-O-(beta-D-galactopyranosyl)-D-gluc.. N,N',N'',N''',N'''',N'''''-Hexaacetylchitohexaose Ginsenoside Rg3 Bromine 5-Bromo-4-chloro-3-indolyl-beta-D-glucuronide cyclohexylammonium salt X-GLUC, NA,X-GLUC SODIUM SALT,X-GlcA CHA salt, X-Gluc CHA salt,X-GlcA Na salt, X-Gluc Na salt 2-ACETAMIDO-1-AZIDO-1-2-DIDEOXY-B-D-GLUC OPYRANOSE

5-BROMO-4-CHLORO-3-INDOLYL-BETA-D-GLUCOPYRANOSIDE (X-GLU)

5-BROMO-4-CHLORO-3-INDOLYL-β-D-GLUCOPYRANOSIDE (X-GLC)

5-BROMO-4-CHLORO-3-INDOLYL-b-D-GLUCO-PYRANOSIDE (X-GLU) extrapure

X-Glc, X-glucoside

(2S,3R,4S,5S,6R)-2-[(5-Bromo-4-chloro-1H-indol-3-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

4-Chloro-5-bromo-1H-indole-3-yl β-D-glucopyranoside

5-Bromo-4-chloro-1H-indol-3-yl β-D-glucopyranoside

5-Bromo-4-chloro-3-indolyl-beta-D-glucoside,98%

(2S,3R,4S,5S,6R)-2-((5-broMo-4-chloro-1H-indol-3-yl)oxy)-6-(hydroxyMethyl)tetrahydro-2H-pyran-3,4,5-triol

5-bromo-4-chloro-3-indolyl-glucopyranoside

GLUC(X-)

5-BROMO-4-CHLORO-3-INDOXYL-BETA-D-GLUCOPYRANOSIDE

5-BROMO-4-CHLORO-3-INDOLYL-BETA-D-GLUCOPYRANOSIDE

5-BROMO-4-CHLORO-3-INDOLYL-BETA-D-GLUCOSIDE

5-Bromo-4-chloro-3-indolyl-beta-D-glucopyranoside 98%

5-Bromo-4-chloro-3-indolyl β-D-glucopyranoside ,98%

5-Bromo-4-chloro-3-indolyl β-D-Glucopyranoside [for Biochemical Research]

X-Glc(X-glucoside、5-Bromo-4-chloro-3-indolyl-β-D-glucopyranoside)

(2S,3R,4S,5S,6R)-2-[(5-Bromo-4-chloro-1H-indol-3-yl)oxy]-6-(hydroxymethyl)tetrahydropyran-3,4,5-triol

5-bromo-4-chloro-3-indolyl β-D-glucoside

X-BETA-D-GLUCOSIDE

X-BETA-D-GLC

X-GLC

X-GLU

X-GLUCOSIDE

5-bromo-4-chloroindol-3-yl-beta-D-glucopyranoside

5-BROMO-4-CHLORO-3-INDOLYLB-D-GLUCOPYRAN OSIDE

X-Gluc(5-Bromo-4-Chloro-3-Indolyl-

5-bromo-4-chloro-3-indoxylglucoside

5-Bromo-4-chloroindolylglucopyranoside

beta-d-glucopyranoside,5-bromo-4-chloro-1h-indol-3-yl

5-BROMO-4-CHLORO-3-INDOLYL-β-D-GLUCOPYRANOSIDE (X-GLU)

β-D-Glucopyranoside, 5-bromo-4-chloro-1H-indol-3-yl

5-Bromo-4-chloro-3-indolyl beta-D-Glucopyranoside [for Biochemical Research]

5-Bromo-4-chloro-3-indolyl-β-D-glucopyranoside

5-Bromo-4-chloro-3-(beta-D-glucopyranosyloxy)indole

5-Bromo-4-chloro-3-indolyl-beta-D-glucoside USP/EP/BP

5-bromo-4-chloro-3-indole- β- D-glucopyranoside

5-bromo-4-chloro-3-indolyl-β-D-glucopyranoside，X-Glu

Bromo-4-Chloro-3-Indolyl-b-D-Glucopyranoside (X-Glu, X-Glc) for tissue culture, 99%

5-Bromo-4-Chloro-3-Indolyl-β-D-Glucopyranoside (X-Glu, X-Glc) for molecular biology, 99%

5-Bromo-4-chloro-3-indolyl-β-D-glucoside

5-Bromo-4-chloro-3-(β-D-glucopyranosyloxy)indole

(5-bromo-4-chloroindol-3-yl) β-D-glucopyranoside

5-Bromo-4-chloro-3-indolyl β-<sc>D</sc>-glucopyranoside

15548-60-4

Plant Molecular Biology

Plant Biotechnology

Substrates, Stains and Detection Kits

Substrates by Enzyme

Enzymes, Inhibitors, and Substrates

Cloning

Enzyme Substrates

Glucosidase, beta-

Biochemicals and Reagents

BioChemical

substrate