D-Gluconic acid sodium salt - ≥97% , CAS No.527-07-1

CAS: 527-07-1 Cat. No.: G305493 Molecular Weight: 218.14 Beilstein Registry Number: 3919651 EC Number: 208-407-7

GRADE & PURITY ≥97%

Synonyms

D-Gluconic acid, sodium salt (1:1) | Gluconic acid, monosodium salt, D- | CAS-527-07-1 | KS-1181 | NCGC00164076-01 | Gluconic acid, sodium salt | CCG-229938 | D-Gluconate sodium salt | SODIUM GLUCONATE [II] | GLUCONIC ACID SODIUM SALT [MI] | sodium (2R,3S

Storage

Room temperature,Desiccated

Shipped In

Normal

Overview

D-Gluconic acid sodium salt has been used:

· as a component to make synthetic interstitial fluid.

· used as a carbohydrate.

· used as a substitute for sodium chloride to make chlorine (Cl-) free media.

Specifications

Synonyms

D-Gluconic acid, sodium salt (1:1) | Gluconic acid, monosodium salt, D- | CAS-527-07-1 | KS-1181 | NCGC00164076-01 | Gluconic acid, sodium salt | CCG-229938 | D-Gluconate sodium salt | SODIUM GLUCONATE [II] | GLUCONIC ACID SODIUM SALT [MI] | sodium (2R, 3S

Specifications & Purity

≥97%

Biochemical and Physiological Mechanisms

D-Gluconic acid is a mild organic acid with non-corrosive, non-odorous, non-volatile and biodegradable property. Enzymatic conversion of D-Glucose results in the final product D-Gluconic acid. Gluconic acid occurs from the oxidation of glucose and is natu

Storage

Room temperature, Desiccated

Shipped In

Normal

Note

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.

Purity

≥97%

Names and Identifiers

• Pubchem Sid: 488200455
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488200455
• Canonical Smiles: C(C(C(C(C(C(=O)[O-])O)O)O)O)O.[Na+]
• IUPAC Name: sodium;(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanoate
• InChIKey: UPMFZISCCZSDND-JJKGCWMISA-M
• INCHI: 1S/C6H12O7.Na/c7-1-2(8)3(9)4(10)5(11)6(12)13;/h2-5,7-11H,1H2,(H,12,13);/q;+1/p-1/t2-,3-,4+,5-;/m1./s1
• Isomeric SMILES: C([C@H]([C@H]([C@@H]([C@H](C(=O)[O-])O)O)O)O)O.[Na+]
• WGK Germany: 1
• RTECS: LZ5235000
• Molecular Weight: 218.14
• Beilstein: 3919651
• Reaxy-Rn: 11330240
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=11330240&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Class Organooxygen compounds
      • Subclass Carbohydrates and carbohydrate conjugates

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Class: Organooxygen compounds
• Subclass: Carbohydrates and carbohydrate conjugates
• Intermediate Tree Nodes: Not available
• Direct Parent: Sugar acids and derivatives
• Alternative Parents: Medium-chain hydroxy acids and derivatives Medium-chain fatty acids Beta hydroxy acids and derivatives Hydroxy fatty acids Monosaccharides Secondary alcohols Carboxylic acid salts Polyols Carboxylic acids Monocarboxylic acids and derivatives Organic oxides Hydrocarbon derivatives Organic sodium salts Organic zwitterions Carbonyl compounds Primary alcohols
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Gluconic_acid - Medium-chain hydroxy acid - Medium-chain fatty acid - Beta-hydroxy acid - Hydroxy fatty acid - Hydroxy acid - Fatty acyl - Fatty acid - Monosaccharide - Carboxylic acid salt - Secondary alcohol - Carboxylic acid derivative - Carboxylic acid - Organic alkali metal salt - Monocarboxylic acid or derivatives - Polyol - Organic sodium salt - Organic oxide - Hydrocarbon derivative - Organic salt - Carbonyl group - Organic zwitterion - Alcohol - Primary alcohol - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as sugar acids and derivatives. These are compounds containing a saccharide unit which bears a carboxylic acid group.
• External Descriptors: organic sodium salt

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)

LMNA Tbio Prelamin-A/C (36751 Activities)

Discover Target: LMNA

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

Associated Targets(non-human)

GCN5 Histone acetyltransferase GCN5 (89 Activities)

Discover Target: GCN5

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

Mechanisms of Action

Chemical and Physical Properties

• Solubility: Very soluble in water; sparingly soluble in alcohol; insoluble in ether.
• Specific Rotation[α]: 13 ° (C=2, H2O)
• Melt Point(°C): 200-205°C
• Molecular Weight: 218.140 g/mol
• Hydrogen Bond Donor Count: 5
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 5
• Exact Mass: 218.04 Da
• Monoisotopic Mass: 218.04 Da
• Topological Polar Surface Area: 141.000 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 176.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 4
• 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

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