Sodium ascorbate - Moligand™, ≥99%, used for (+)-Sodium L-ascorbate has been used: as a component of cutting solution for storing brain slices of rats. As a component of patch pipette internal solution for imaging Ca2+ transients evoked by action potentia

CAS: 134-03-2 Cat. No.: S105024 Formula: C₆H₇NaO₆ Molecular Weight: 198.11 Beilstein Registry Number: 3767246 EC Number: 205-126-1 PubChem CID: 23667548

GRADE & PURITY Moligand™, ≥99%

Synonyms

Vitamin C Sodium Salt | Natrii ascorbas | Monosodium L-ascorbate | L-Ascorbic acid sodium salt | Natri-C | Sodascorbate | Ascorbicin | Ascorbate de sodium | Vitamin C sodium | Iskia-C | Sodium L-ascorbate | Ascorbic acid sodium salt | (+)-Sodium L-ascorba

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Overview

Ascorbic acid, also known as vitamin C, is a water-soluble vitamin. L-Ascorbic acid is a reducing agent.

Specifications

Synonyms

Vitamin C Sodium Salt | Natrii ascorbas | Monosodium L-ascorbate | L-Ascorbic acid sodium salt | Natri-C | Sodascorbate | Ascorbicin | Ascorbate de sodium | Vitamin C sodium | Iskia-C | Sodium L-ascorbate | Ascorbic acid sodium salt | (+)-Sodium L-ascorba

Specifications & Purity

Moligand™, ≥99%

Biochemical and Physiological Mechanisms

Ascorbic acid exhibits anti-oxidant properties. It is a primary substrate for detoxifying hydrogen peroxide. Ascorbic acid is a co-factor for the synthesis of adrenal steroids and catecholamines. L-Ascorbic acid (Vitamin C) is a water soluble molecule use

Application

(+)-Sodium L-ascorbate has been used: as a component of cutting solution for storing brain slices of rats. As a component of patch pipette internal solution for imaging Ca2+ transients evoked by action potential in rat brain slices. As a supplement for ar

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Grade

Moligand™

Purity

≥99%

Names and Identifiers

Pubchem Sid

488200428

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/488200428

Canonical Smiles

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

IUPAC Name

sodium;(2R)-2-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-5-oxo-2H-furan-3-olate

InChIKey

PPASLZSBLFJQEF-RXSVEWSESA-M

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

Isomeric SMILES

C([C@@H]([C@@H]1C(=C(C(=O)O1)O)[O-])O)O.[Na+]

WGK Germany

1

RTECS

CI7671000

PubChem CID

23667548

Molecular Weight

198.11

Beilstein

3767246

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Dihydrofurans
      • Subclass Furanones

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Dihydrofurans
• Subclass: Furanones
• Intermediate Tree Nodes: Not available
• Direct Parent: Butenolides
• Alternative Parents: Vinylogous acids Enoate esters Secondary alcohols Lactones 1,2-diols Oxacyclic compounds Monocarboxylic acids and derivatives Primary alcohols Organic zwitterions Organic sodium salts Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: 2-furanone - Enoate ester - Alpha,beta-unsaturated carboxylic ester - Vinylogous acid - 1,2-diol - Carboxylic acid ester - Lactone - Secondary alcohol - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Oxacycle - Organic alkali metal salt - Hydrocarbon derivative - Organic oxide - Organic zwitterion - Organic oxygen compound - Primary alcohol - Organooxygen compound - Alcohol - Carbonyl group - Organic salt - Organic sodium salt - Aliphatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as butenolides. These are dihydrofurans with a carbonyl group at the C2 carbon atom.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

FFAR3 Tchem Free fatty acid receptor 3 (304 Activities)

Discover Target: FFAR3

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CRYAB Tchem Alpha-crystallin B chain (132 Activities)

Discover Target: CRYAB

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Sensitivity: Light & Moisture &Air sensitive
• x_specific_rotation: 105.5 ° (C=10, H2O)
• x_melt_point_char: 219-221°C
• Molecular Weight: 198.110 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 198.014 Da
• Monoisotopic Mass: 198.014 Da
• Topological Polar Surface Area: 110.000 Ų
• Heavy Atom Count: 13
• Formal Charge: 0
• Complexity: 237.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 2
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 2

XLogP3