Products for Research Use Only

Sodium ascorbate

CAT: 0013-GTR19159683-01Size: 500 mgDry Ice: NoHazardous: No
Product image 1
1 / 1
CAT#:0013-GTR19159683-01Size:500 mg
Selected
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
Quick Request Actions
Description
Ascorbate, also known as Ascorbicin, is a DNase I inhibitor. Ascorbate is an antioxidant which functions as a reducing agent and coenzyme in several metabolic pathways. (In Vitro) :The conditioned medium for B16F10 cells significantly inhibits cell apoptosis induced by L-Ascorbic acid sodium salt (Sodium L-ascorbate) (10 mM), and the effective ingredients in the medium show a relative molecular mass below 5,000. (In Vivo) :Tg rats treated with L-Ascorbic acid sodium salt (Sodium L-ascorbate) show a higher incidence of carcinoma (29.6%), compared to those without L-Ascorbic acid sodium salt (15.4%) . Independent of the L-Ascorbic acid sodium salt treatment, transgenic rats exhibit various kinds of malignant tumors in various organs.After 12 weeks of PEITC-treatment, both simple hyperplasia and papillary or nodular (PN) hyperplasia have developed in all animals, but the majority of these lesions have disappeared at week 48, irrespective of the L-Ascorbic acid sodium salt-treatment. The same lesions after 24 weeks of PEITC-treatment have progressed to dysplasia and carcinoma, in a small number of cases by week 48, but enhancement by the L-Ascorbic acid sodium salt-treatment is evident only with simple hyperplasias and PN hyperplasias in rats.
CAS Number
134-03-2
Product Name Alternative
Ascorbate | Sodium Ascorbate | Vitamin C sodium
Purity
>98% (HPLC)
Solubility
H2O : ≥ 41 mg/mL; 206.96 mM
Smiles
[Na].[H][C@@]1 (OC (=O) C (O) C1O) [C@@H] (O) CO
Molecular Formula
C6H8O6·Na
Molecular Weight
201.13
Storage Conditions
Storage temperature: -20°C. Stability: ≥ 2 years
Notes
For research use only.
Other Product Names
Sodium (2R) -2-[ (1S) -1,2-dihydroxyethyl]-4-hydroxy-5-oxo-2H-furan-3-olate

Chemical Information

Sodium Ascorbate

Sodium ascorbate is an organic sodium salt resulting from the replacement of the proton from the 3-hydroxy group of ascorbic acid by a sodium ion. It has a role as a coenzyme, a reducing agent, a flour treatment agent, a plant metabolite, a human metabolite, a food antioxidant and a Daphnia magna metabolite. It is a vitamin C and an organic sodium salt. It contains a L-ascorbate.

CAS Number134-03-2
PubChem CID23667548
IUPAC Namesodium (2R)-2-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-5-oxo-2H-furan-3-olate
Molecular FormulaC6H7NaO6
Molecular Weight198.11
Topological Polar Surface Area110
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count6
Rotatable Bond Count2
Heavy Atom Count13
Formal Charge0
Complexity237
SMILES
C([C@@H]([C@@H]1C(=C(C(=O)O1)O)[O-])O)O.[Na+]
InChI
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
InChIKey
PPASLZSBLFJQEF-RXSVEWSESA-M
Chemical Structure
2D Structure
2D structure of Sodium Ascorbate
CAS: 134-03-2
CID: 23667548
Formula: C6H7NaO6
MW: 198.11
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight198.11
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count6
Rotatable Bond Count2
Exact Mass198.01403222
Monoisotopic Mass198.01403222
Topological Polar Surface Area110 Ų
Heavy Atom Count13
Formal Charge0
Complexity237
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count2
Compound Is CanonicalizedYes