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Supplier NameMedChemExpress (MCE)
Contactsales
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Mobile609-228-6898
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Emailsales@medchemexpress.com; tech@medchemexpress.com
Websitehttps://www.medchemexpress.com/
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Product Name5-bromo-4-chloro-3-indolyl-N-acetyl-B-D-galactosaminide
SynonymsX-GALNAC
X-BETA-D-GALNAC
X-GalactosaMidide
X-N-ACETYL-GALACTOSAMINIDE
X-N-ACETYL-BETA-D-GALACTOSAMINIDE
N-Acetyl-5-bromo-4-chloro-3-indolyl--D-galactosaminide
5-bromo-4-chloro-3-indolyl-N-acetyl-B-D-galactosaminide

Synonyms

X-GALNAC
X-BETA-D-GALNAC
X-GalactosaMidide
X-N-ACETYL-GALACTOSAMINIDE
X-N-ACETYL-BETA-D-GALACTOSAMINIDE
N-Acetyl-5-bromo-4-chloro-3-indolyl--D-galactosaminide
5-bromo-4-chloro-3-indolyl-N-acetyl-B-D-galactosaminide
5-Bromo-4-chloro-3-indoxyl-N-acetyl-∫-D-galactosaminide
5-Bromo-4-chloro-3-indolyl N-acetyl-beta-D-galactosaminide
5-BROMO-4-CHLORO-3-INDOLYL-N-ACETYL-BETA-D-GALACTOSAMINIDE
5-BROMO-4-CHLORO-3-INDOXYL-N-ACETYL-BETA-D-GALACTOSAMINIDE
5-bromo-4-chloro-1H-indol-3-yl 2-(acetylamino)-2-deoxy-beta-D-glucopyranoside
5-bromo-4-chloro-1H-indol-3-yl 2-(acetylamino)-2-deoxy-beta-D-galactopyranoside
CAS129572-48-1
EINECS1533716-785-6
Chemical FormulaC16H18BrClN2O6
Molecular Weight449.68
inchiInChI=1/C16H18BrClN2O6/c1-7(22)20-12-14(24)13(23)10(5-21)25-15(12)26-16(17)6-19-9-4-2-3-8(18)11(9)16/h2-4,6,10,12-15,21,23-24H,5H2,1H3,(H,20,22)/t10-,12-,13+,14-,15?,16?/m1/s1
Package25 mg;50 mg
PriceEmail to quote
DescriptionsX-GalNAc

X-GalNAc

MedChemExpress (MCE)

HY-W116594

129572-48-1

99.72%

-20°C, protect from light *In solvent : -80°C, 6 months

Descriptions

X-GalNAc

X-GalNAc

MedChemExpress (MCE)

HY-W116594

129572-48-1

99.72%

-20°C, protect from light *In solvent : -80°C, 6 months
-20°C, 1 month (protect from light)

Room temperature in continental US
may vary elsewhere.

X-GalNAc is a chromogenic substrate for for N-acetyl-β-galactosidase, used to determine the presence or absence of a cloned DNA insert in bacteria growing on agar plates.

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[1]. Smith WS, et al. Applying neutral drift to the directed molecular evolution of a β-glucuronidase into a β-galactosidase: Two different evolutionary pathways lead to the same variant. BMC Res Notes. 2011 May 6
4:138.

[2]. Semen A Leyn, et al. N-acetylgalactosamine utilization pathway and regulon in proteobacteria: genomic reconstruction and experimental characterization in Shewanella. J Biol Chem. 2012 Aug 10
287(33):28047-56.
[Content Brief]

Supplier Websitehttps://www.medchemexpress.com/x-galnac.html
Last Update2025-05-21 16:50:25
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