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ChemicalBook--->CAS DataBase List--->527-07-1

527-07-1

527-07-1 Structure

527-07-1 Structure
IdentificationMore
[Name]

Sodium gluconate
[CAS]

527-07-1
[Synonyms]

2,3,4,5,6-PENTAHYDROXYCAPROIC ACID SODIUM SALT
D-GLUCONATE SODIUM SALT
D-GLUCONIC ACID MONOSODIUM SALT
D-GLUCONIC ACID SODIUM SALT
D-GLUTONIC ACID SODIUM SALT
GLUCONIC ACID SODIUM SALT
SODIUM D-GLUCONATE
SODIUM GLUCONATE
Developer,partB
glonsen
gluconatodisodio
monosodiumgluconate
monosodiumsalt,d-gluconicaci
pasexon100t
pmpsodiumgluconate
Gluconic Acid Sodium
SODIUM GLUCONATE RE
sodium pentahydyoxycaproate
Sodium Gluconate USP26 FCCIV
SODIUM GLUCONATE USP
[EINECS(EC#)]

208-407-7
[Molecular Formula]

C6H11NaO7
[MDL Number]

MFCD00064210
[Molecular Weight]

218.14
[MOL File]

527-07-1.mol
Chemical PropertiesBack Directory
[Appearance]

white or off-white granular powder
[Melting point ]

170-175 °C
[alpha ]

[α]D20 +11~+13° (c=10, H2O)
[storage temp. ]

Store below +30°C.
[solubility ]

H2O: 0.1 g/mL, clear
[form ]

Crystalline Powder
[color ]

White to light beige
[Odor]

wh. to ylsh. cryst. powd., pleasant odor
[PH]

7.0-8.0 (100g/l, H2O, 20℃)
[Stability:]

Stable. Incompatible with strong oxidizing agents.
[Water Solubility ]

Very soluble in water; sparingly soluble in alcohol; insoluble in ether.
[Merck ]

14,4456
[BRN ]

3919651
[InChI]

InChI=1/C6H12O7.Na.H/c7-1-2(8)3(9)4(10)5(11)6(12)13;;/h2-5,7-11H,1H2,(H,12,13);;/t2-,3-,4+,5-;;/s3
[InChIKey]

MPPJUDJABRMYJR-QZHCVFHNNA-N
[SMILES]

[C@@H](O)([C@@H](O)C(=O)O)[C@H](O)[C@H](O)CO.[NaH] |&1:0,2,7,9,r|
[LogP]

-3.175 (est)
[CAS DataBase Reference]

527-07-1(CAS DataBase Reference)
[EPA Substance Registry System]

527-07-1(EPA Substance)
Safety DataBack Directory
[Safety Statements ]

S24/25:Avoid contact with skin and eyes .
[WGK Germany ]

1
[RTECS ]

LZ5235000
[Autoignition Temperature]

>200 °C
[TSCA ]

Yes
[HS Code ]

29181600
[Safety Profile]

Low toxicity by intravenous route. When heated to decomposition it emits acrid smoke and irritating fumes
[Toxicity]

LD50 orally in Rabbit: > 2000 mg/kg
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Sodium hydroxide-->Sodium carbonate-->D(+)-Glucose-->Calcium gluconate-->Gluconic acid-->D-Glucose monohydrate
[Preparation Products]

Calcium gluconate-->Copper(II) gluconate-->Zinc gluconate-->Sodium Stibogluconate
Material Safety Data Sheet(MSDS)Back Directory
[msds information]

Gluconic acid sodium salt(527-07-1).msds
Hazard InformationBack Directory
[Description]

Sodium gluconate is the organic sodium salt of gluconic acid. Sodium gluconate is a chelator that forms stable complexes with various ions and ultimately prevents these ions from engaging in chemical reactions. Gluconates are naturally occurring substances that freely dissociate to the gluconate anion and its respective cations. Being fully biodegradable and non-toxic, it represents an environment friendly alternative to the common chelating agents used in cosmetics such as EDTA. In addition to this, sodium gluconate has a low acute toxicity to aquatic organisms.
[Chemical Properties]

white or off-white granular powder
[Originator]

Sodium gluconate,JUNGBUNZLAUER INC.
[Uses]

Sodium gluconate is used as a natural preservative. It prevents the growth of microbes in our products to keep them safe for our consumers. It also works as a skin-conditioning agent and a chelating agent which helps cleansing products to foam better in hard water. You can often find sodium gluconate in soap, sunscreen, shampoo, toothpaste, hair products, makeup, and a variety of other personal care products.
Sodium gluconate has been used as a component of recording buffer used in two-electrode voltage-clamp (TEVC) recording in Xenopus laevis oocytes. It has also been used as a control for sodium.
[Definition]

ChEBI: An organic sodium salt having D-gluconate as the counterion.
[Production Methods]

Sodium gluconate is manufactured by the fermentation of carbohydrate containing the raw material glucose syrup derived from maize. After a crystallisation step, sodium gluconate is separated from the mother liquor by centrifugation, the crystals are dried and then sieved to guarantee the desired granulation. Based on the production process as well as the raw materials used, sodium gluconate is not synthetic natural.
[Manufacturing Process]

D-Gluconic acid was prepared by fermentation of glucose with Aspergillus niger CCM 8004 at 30°C. The fermentation medium contained 150 g/dm-3 glucose, 0.59 g/dm-3 ammonium sulfate, 0.25 g/dm-3 potassium chloride, 0.25 g/dm-3 potassium dihydrophosphate, 0.25 g/dm-3 MgSO4·7H2O, 1.0 g/dm-3 Ca(NO3)2·4H2O, and 1.5 g/dm-3 of a 50% corn-steep liquor. The pH of the culture was maintained at the value of 6.5 during the growth phase and 5.5 (maximum glucose oxidase activity) during the production phase by addition of 11.7 M sodium hydroxide solution. Gluconic acid concentration was determined by HPLC analysis. By neutralization of D-gluconic acid with sodium hydroxide was obtained monosodium D-gluconate.
[Therapeutic Function]

Electrolyte replenisher
[General Description]

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.
[Biochem/physiol Actions]

Ingestion of sodium gluconate is known to stimulate the production of intestinal butyrate. It is widely used in food, pharmaceutical paper and textile industry. It acts as a chelating agent. Sodium gluconate serves as a detergent in bottle washing formulation.
[Synthesis]

The calcium gluconate is added into the reaction kettle. Add sulfuric acid aqueous solution while stirring. After mixing for one hour, let it stand for a while and then get it filtered. The filter residue is CaSO4 and gets it removed. The filtrate is added into the neutralization kettle, and a proper amount of Na2CO3 aqueous solution is added to neutralize it. Finally get sodium gluconate through concentration, filtration and drying.
[Purification Methods]

Crystallise it from a small volume of H2O (solubility is 59g/100mL at 25o), or dissolve it in H2O and add EtOH since it is sparingly soluble in EtOH. It is insoluble in Et2O. It forms a Cu complex in alkaline solution and a complex with Fe in neutral solution. [cf p 639, Sawyer & Bagger J Am Chem Soc 81 5302 1959, Beilstein 3 I 188.]
[Regulations]

In Europe, sodium gluconate is listed as a generally permitted food additive (E576) and may be added to all foodstuffs, following the "quantum satis" principle, as long as no special regulation restricts the use.
The US Food and Drug Administration (FDA) assigned sodium gluconate the “generally recognised as safe” (GRAS) status and permitted its use in food without limitation other than current good manufacturing practice.
Sodium gluconate is exempted from the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) by means of Commission Regulation (EC) No. 987/2008 of 8 October, 2008 (amending Annex IV). As a consequence thereof, there is no need to register sodium gluconate.
Spectrum DetailBack Directory
[Spectrum Detail]

Sodium gluconate(527-07-1)1HNMR
Sodium gluconate(527-07-1)13CNMR
Sodium gluconate(527-07-1)IR1
Sodium gluconate(527-07-1)IR2
Sodium gluconate(527-07-1)Raman
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

Gluconic acid, sodium salt, 98%(527-07-1)
[Alfa Aesar]

Sodium D-gluconate, 97%(527-07-1)
[Sigma Aldrich]

527-07-1(sigmaaldrich)
[TCI AMERICA]

Sodium Gluconate,>99.0%(T)(527-07-1)
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