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V900326

Sigma-Aldrich

(+)-Sodium L-ascorbate

Vetec, reagent grade, 98%

Synonym(s):

L(+)-Ascorbic acid sodium salt, Vitamin C sodium salt

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About This Item

Empirical Formula (Hill Notation):
C6H7NaO6
CAS Number:
Molecular Weight:
198.11
Beilstein:
3767246
EC Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:

grade

reagent grade

product line

Vetec

Assay

98%

form

powder

color

white to off-white

mp

220 °C (dec.) (lit.)

SMILES string

[Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-]

InChI

1S/C6H8O6.Na/c7-1-2(8)5-3(9)4(10)6(11)12-5;/h2,5,7-10H,1H2;/q;+1/p-1/t2-,5+;/m0./s1

InChI key

PPASLZSBLFJQEF-RXSVEWSESA-M

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General description

Sodium L-ascorbate is an ascorbate derivative.

Biochem/physiol Actions

Sodium L-ascorbate favors apoptosis in urinary bladder carcinoma. It reduces reactive oxygen species generation and plays a role in elastogenesis. In addition, it improves mRNA levels of tropoelastin contributing to skin remodeling. Sodium L-ascorbate may serve as a potential therapeutic potential and may be used in combination with collagenogenesis inhibitorsfor treating dermal scars and keloids. It has wide applications in the food industry as an antioxidant and preservative. Sodium ascorbate also elicits protection by stabilizing membrane, lowering lipid peroxidation and enhancing total antioxidant content.

Legal Information

Vetec is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class Code

11 - Combustible Solids

WGK

WGK 1


Certificates of Analysis (COA)

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Oxidative Stress and Chronic Degenerative Diseases-A Role for Antioxidants, 75(3), 449-449 (2013)
Vitamin C and Trolox decrease oxidative stress and hemolysis in cold-stored human red blood cells
Czubak K, et al.
Redox Report, 22(6), 445-450 (2017)
Significant overexpression of metallothionein and cyclin D1 and apoptosis in the early process of rat urinary bladder carcinogenesis induced by treatment with N-butyl-N-(4-hydroxybutyl) nitrosamine or sodium L-ascorbate
Takaba K, et al.
Carcinogenesis, 21(4), 691-700 (2000)
Lin Zhang et al.
Biosensors & bioelectronics, 69, 77-82 (2015-02-24)
A novel label-free nanosensor has been developed for detecting biothiols including cysteine, glutathione and homocysteine based on poly(thymine)-templated fluorescent copper nanoparticles (CuNPs), which were controlled through thymine-Hg(II)-thymine coordination. This assay provides a simple, cost-effective, and sensitive platform for the detection

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