Sodium ascorbate structure, CAS 134-03-2

Sodium ascorbate

CAS Number134-03-2

SynonymsEINECS 205-126-1; Sodium ascorbate; L-Ascorbic Acid Sodium Salt; Vitamine C sodium salt,Vitamin C sodium salt; (+)-Sodium L-ascorbate (L(+)-Ascorbic acid sodium salt; SodiuM L-Ascorbate; L(+)-Ascorbic acid sodium salt,Vitamin C sodium salt; MFCD00082340; Vitamin C Sodium Salt; L(+)-Ascorbic acid sodium salt,E301

Molecular FormulaC6H7NaO6

Molecular Weight198.11

Purity≥98%

Density1.799 g/cm3

Boiling Point552.7ºC at 760 mmHg

Melting Point220 °C (dec.) (lit.)

Flash Point

Appearancecrystalline

EINECS205-126-1

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Cat. No.: 2A-9020718 Purity: ≥98%
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Chemical & Physical Properties
CAS Number134-03-2
Catalog No.2A-9020718
Chinese Name维生素C钠
SynonymsEINECS 205-126-1; Sodium ascorbate; L-Ascorbic Acid Sodium Salt; Vitamine C sodium salt,Vitamin C sodium salt; (+)-Sodium L-ascorbate (L(+)-Ascorbic acid sodium salt; SodiuM L-Ascorbate; L(+)-Ascorbic acid sodium salt,Vitamin C sodium salt; MFCD00082340; Vitamin C Sodium Salt; L(+)-Ascorbic acid sodium salt,E301
Molecular FormulaC6H7NaO6
Molecular Weight198.11
Purity≥98
Density1.799 g/cm3
Boiling Point552.7ºC at 760 mmHg
Melting Point220 °C (dec.) (lit.)
Appearancecrystalline
Water Solubility620 g/L (20 ºC)
Storage ConditionStore sealed and away from light.
ApplicationL-Ascorbic acid sodium is the more available form of vitamin C and has antioxidant effects.
EINECS205-126-1
PubChem ID24891261
MDL NumberMFCD00082340
SMILES[Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-]
InChI1S/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 KeyPPASLZSBLFJQEF-RXSVEWSESA-M
Beilstein/REAXYS3767246
NACRES CodeNA.79
eCl@ss34058010
UNSPSC12352205
Hazard SymbolsTransport
MSDSmsds/20718_1_134_03_2.pdf
BioactivityL-Ascorbic acid (sodium) is a more bioavailable form of vitamin C that is an antioxidant agent. Related Catalog Signaling Pathways >> Others >> Others Research Areas >> Cancer Natural Products >> Others In Vitro Vitamin C (L-ascorbic acid), a known enhancer of collagen deposition, has also been identified as an inhibitor of elastogenesis[1]. The conditioned medium for B16F10 cells significantly inhibits cell apoptosis induced by sodium L-ascorbate (10 mM), and the effective ingredients in the medium show a relative molecular mass below 5,000[2]. In Vivo Tg rats treated with sodium L-ascorbate show a higher incidence of carcinoma (29.6%), compared to those without sodium L-ascorbate (15.4%). Independent of the sodium L-ascorbate treatment, transgenic rats exhibit various kinds of malignant tumors in various organs[3]. 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 sodium L-ascorbate-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 sodium L-ascorbate-treatment is evident only with simple hyperplasias and PN hyperplasias in rats[4]. Animal Admin A total of 40 7-week-old male Tg rats are divided into 2 groups. Twenty-seven (group 1) and 13 (group 2) rats are given a powdered MF diet with or without 5% sodium L-ascorbate, respectively. Similarly, a total of 42 7-week-old male Non-tg rats are divided into 2 groups, and 30 (group 3) and 12 (group 4) animals are given a diet with or without 5% sodium L-ascorbate, respectively. References [1]. Hinek A, et al. Sodium L-ascorbate enhances elastic fibers deposition by fibroblasts from normal and pathologic human skin. J Dermatol Sci. 2014 Sep;75(3):173-82. [2]. Yang X, et al. Mouse melanoma cell line B16F10-derived conditioned medium inhibits sodium L-ascorbate-induced B16F10 cell apoptosis. Nan Fang Yi Ke Da Xue Xue Bao. 2012 Feb;32(2):146-50. [3]. Morimura K, et al. Lack of urinary bladder carcinogenicity of sodium L-ascorbate in human c-Ha-ras proto-oncogene transgenic rats. Toxicol Pathol. 2005;33(7):764-7. [4]. Takagi H, et al. Limited tumor-initiating activity of phenylethyl isothiocyanate by promotion with sodium L-ascorbate in a rat two-stage urinary bladder carcinogenesis model. Cancer Lett. 2005 Mar 10;219(2):147-53. Chemical & Physical Properties Density 1.799 g/cm3 Boiling Point 552.7ºC at 760 mmHg Melting Point 220 °C (dec.)(lit.) Molecular Formula C6H7NaO6 Molecular Weight 198.106 Flash Point 238.2ºC Exact Mass 198.014038 PSA 110.05000 Vapour Pressure 1.62E-14mmHg at 25°C Index of Refraction 105.5 ° (C=10, H2O) InChIKey PPASLZSBLFJQEF-RXSVEWSESA-M SMILES O=C1OC(C(O)CO)C([O-])=C1O.[Na+] Water Solubility 620 g/L (20 ºC)
Use ofL-Ascorbic acid (sodium) is a more bioavailable form of vitamin C that is an antioxidant agent. Properties Articles170 Name Sodium L-Ascorbate Synonym More Synonyms sodium ascorbate Biological Activity Description L-Ascorbic acid (sodium) is a more bioavailable form of vitamin C that is an antioxidant agent. Related Catalog Signaling Pathways >> Others >> Others Research Areas >> Cancer Natural Products >> Others In Vivo Tg rats treated with sodium L-ascorbate show a higher incidence of carcinoma (29.6%), compared to those without sodium L-ascorbate (15.4%). Independent of the sodium L-ascorbate treatment, transgenic rats exhibit various kinds of malignant tumors in various organs[3]. 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 sodium L-ascorbate-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 sodium L-ascorbate-treatment is evident only with simple hyperplasias and PN hyperplasias in rats[4]. References [1]. Hinek A, et al. Sodium L-ascorbate enhances elastic fibers deposition by fibroblasts from normal and pathologic human skin. J Dermatol Sci. 2014 Sep;75(3):173-82. [3]. Morimura K, et al. Lack of urinary bladder carcinogenicity of sodium L-ascorbate in human c-Ha-ras proto-oncogene transgenic rats. Toxicol Pathol. 2005;33(7):764-7. [4]. Takagi H, et al. Limited tumor-initiating activity of phenylethyl isothiocyanate by promotion with sodium L-ascorbate in a rat two-stage urinary bladder carcinogenesis model. Cancer Lett. 2005 Mar 10;219(2):147-53. Chemical & Physical Properties Molecular Formula C6H7NaO6 Exact Mass 198.014038 PSA 110.05000 InChIKey PPASLZSBLFJQEF-RXSVEWSESA-M SMILES O=C1OC(C(O)CO)C([O-])=C1O.[Na+]
Transport InfoShipping Name: UN
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 United Nations shipping name European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Danger Regulations: No International Maritime Danger Regulations International Air Transport Danger Regulations: No Marine pollutants (yes/no): No 14.6 Special reminder to users No data available
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