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Merck

P4902

Sigma-Aldrich

2-Phenylethyl β-D-thiogalactoside

≥98% (TLC)

Sinónimos:

PETG, Phenethyl β-D-thiogalactoside

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About This Item

Fórmula empírica (notación de Hill):
C14H20O5S
Número de CAS:
Peso molecular:
300.37
Beilstein:
20033
Número MDL:
Código UNSPSC:
12352201
ID de la sustancia en PubChem:
NACRES:
NA.25

Nivel de calidad

Ensayo

≥98% (TLC)

Formulario

powder

actividad óptica

[α]/D -33.00 to -27.00°, c = 9.00-11.00 mg/mL in methanol

técnicas

thin layer chromatography (TLC): suitable

color

white

solubilidad

methanol: 49.00-51.00 mg/mL, clear, colorless

temp. de almacenamiento

2-8°C

cadena SMILES

OC[C@H]1O[C@@H](SCCc2ccccc2)[C@H](O)[C@@H](O)[C@H]1O

InChI

1S/C14H20O5S/c15-8-10-11(16)12(17)13(18)14(19-10)20-7-6-9-4-2-1-3-5-9/h1-5,10-18H,6-8H2/t10-,11+,12+,13-,14+/m1/s1

Clave InChI

ZNAMMSOYKPMPGC-HTOAHKCRSA-N

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Descripción general

2-Phenylethyl β-D-thiogalactoside is a cell-permable inhibitor of the reporter enzyme β-galactosidase.

Aplicación

2-Phenylethyl β-D-thiogalactoside has been used in a study to assess subnanoliter enzymatic assays on microarrays. It has also been used in a study that investigated the integration of on-column immobilized enzyme reactor in microchip electrophoresis.

Otras notas

To gain a comprehensive understanding of our extensive range of Monosaccharides for your research, we encourage you to visit our Carbohydrates Category page.

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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Kyung-Han Lee et al.
European journal of nuclear medicine and molecular imaging, 31(3), 433-438 (2004-01-28)
There has recently been increasing interest in the development of radioprobes that specifically target proteins transcribed from expression of reporter genes of interest. The purpose of this study was to develop a radioprobe that targets one of the most widely
Todd Galbraith et al.
Biotechnology journal, 14(1), e1800306-e1800306 (2018-11-30)
There is a strong clinical need to develop small-caliber tissue-engineered blood vessels for arterial bypass surgeries. Such substitutes can be engineered using the self-assembly approach in which cells produce their own extracellular matrix (ECM), creating a robust vessel without exogenous
Pranav R H Joshi et al.
Molecular therapy. Methods & clinical development, 13, 279-289 (2019-03-20)
Despite numerous advancements in production protocols, manufacturing AAV to meet exceptionally high demand (1016-1017 viral genomes [VGs]) in late clinical stages and for eventual systemic delivery poses significant challenges. Here, we report an efficient, simple, scalable, robust AAV5 production process
Nectarios Vidakis et al.
Polymers, 12(12) (2020-12-10)
In this study, the strain rate sensitivity of five different thermoplastic polymers processed via Fused Filament Fabrication (FFF) Additive Manufacturing (AM) is reported. Namely, Polylactic Acid (PLA), Acrylonitrile-Butadiene-Styrene (ABS), Polyethylene Terephthalate Glycol (PETG), Polyamide 6 (PA6), and Polypropylene (PP) were
R A Edwards et al.
Biochemistry, 29(49), 11001-11008 (1990-12-11)
The thermal denaturation of wild-type beta-galactosidase and two beta-galactosidases with substitutions at the active site was studied by kinetics, differential scanning calorimetry, electrophoresis, molecular exclusion chromatography, and circular dichroism. From the results, a model is developed for thermal denaturation of

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