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G2164

Sigma-Aldrich

Gluconolactone

99.0-101.0%, meets USP testing specifications

Sinónimos:

D-(+)-Gluconic acid δ-lactone, δ-Gluconolactone, 1,2,3,4,5-Pentahydroxycaproic acid δ-lactone, D-(+)-Dextronic acid δ-lactone

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About This Item

Fórmula empírica (notación de Hill):
C6H10O6
Número de CAS:
90-80-2
Peso molecular:
178.14
Beilstein:
83286
Número CE:
202-016-5
Número MDL:
MFCD00006647
Código UNSPSC:
12352201
ID de la sustancia en PubChem:
24895089
NACRES:
NA.21

origen biológico

corn

Nivel de calidad

200

Agency

USP/NF
meets USP testing specifications

Análisis

99.0-101.0%

formulario

crystalline

color

white

mp

160 °C (dec.) (lit.)

solubilidad

water: soluble

aplicaciones

pharmaceutical (small molecule)

cadena SMILES

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

InChI

1S/C6H10O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-5,7-10H,1H2/t2-,3-,4+,5-/m1/s1

Clave InChI

PHOQVHQSTUBQQK-SQOUGZDYSA-N

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Descripción general

Gluconolactone is a non-toxic component of the skin. It has anti-oxidant and free radical scavenging effects. Gluconolactone has antiaging and skin-firming properties. It acts as a β-glucosidase inhibitor. Gluconolactone stimulates cellulase gene expression.

Aplicación

Gluconolactone has been used:
  • to control the acidification kinetics of natural rubber latex (NRL) suspensions
  • to study its effects on inhibition and disintegration of collagen fibrils
  • to prepare alginate hydrogel

Acciones bioquímicas o fisiológicas

Glucono-d-lactone increased the doubling time and activated enzymes involved in the oxidative pentose phosphate pathway of Saccharomyces cerevisiae.

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 1

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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Certificados de análisis (COA)

Lot/Batch Number
0000389966
0000389964
0000389965
0000387454
0000389963

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Visite la Librería de documentos

Acid-induced aggregation and gelation of natural rubber latex particles
de Oliveira Reis G, et al.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 482(68), 9-17 (2015)
Procedures in Cosmetic Dermatology Series: Cosmeceuticals E-Book (2008)
Gluconolactone induces cellulase gene expression in cellulolytic filamentous fungus Trichoderma reesei
Kou Y, et al.
Royal Society of Chemistry Advances, 4(68), 36057-36063 (2014)
Guilherme de Oliveira Reis et al.
Journal of colloid and interface science, 539, 287-296 (2018-12-28)
Natural rubber is obtained by processing natural rubber latex, a liquid colloidal suspension that rapidly gels after exudation from the tree. We prepared such gels by acidification, in a large range of particle volume fractions, and investigated their rheological properties.
A Grygorczyk et al.
Food chemistry, 141(3), 1716-1721 (2013-07-23)
The objective of this work was to compare the gelation of soymilk particles induced by the acidification of a commercial starter culture with that resulting by addition of glucono-δ-lactone (GDL). Structure formation was followed using rheology, and the microstructure was
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