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134-03-2

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134-03-2 Usage

Description

Sodium ascorbate is sodium salt of ascorbic acid (commonly known as vitamin C), which is approved for use as a food additive in many countries. Sodium ascorbate is consisted of a combination of sodium and vitamin C, which commonly serve as an antioxidant and an acidity regulator in pharmaceutical manufacturing and in the food industry. In this mixture, sodium acts as a buffer, creating a less acidic supplement than those made entirely from vitamin C. It can be easier to tolerate if the digestive system is sensitive to acid. As a vitamin C supplement, it provides both sodium and vitamin C for human body, which is effective to prevent or treat vitamin C deficiency. Besides, studies have shown that taking sodium ascorbate is helpful with cancer prevention and treatment.

References

https://en.wikipedia.org/wiki/Sodium_ascorbate http://www.livestrong.com/article/348175-what-are-the-health-benefits-of-sodium-ascorbate/ http://pets.webmd.com/drugs/2/drug-63684/ascorbic-acid-ascorbate-sodium-oral/details

Chemical Properties

Sodium ascorbate occurs as a white or slightly yellow-colored, practically odorless, crystalline powder with a pleasant saline taste.

Uses

Different sources of media describe the Uses of 134-03-2 differently. You can refer to the following data:
1. Sodium Ascorbate is an antioxidant that is the sodium form of ascorbic acid. it is soluble in water and provides a nonacidic taste. a 10% aqueous solution has a ph of 7.3–7.6. in water, it readily reacts with atmospheric oxygen and other oxidizing agents, making it valuable as an antioxidant. one part sodium ascorbate is equivalent to 1.09 parts of sodium erythorbate. see ascorbic acid.
2. L-Ascorbic acid (Vitamin C) is a water soluble molecule used in a wide variety of applications, including cell culture, as a reducing agent that helps reduce oxidative stress.
3. As antimicrobial and antioxidant in foodstuffs.

Definition

ChEBI: 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 food antioxidant, a flour treatment agent, a coenzyme, a plant metabolite, a human metabolite, a Daphnia magna metabolite and a reducing agent. It is an organic sodium salt and a vitamin C. It contains a L-ascorbate.

Production Methods

An equivalent amount of sodium bicarbonate is added to a solution of ascorbic acid in water. Following the cessation of effervescence, the addition of propan-2-ol precipitates sodium ascorbate.

Brand name

Ascorbin (Marion Merrell Dow).

General Description

Minute crystals or white powder. pH of aqueous solutions 5.6 to 7.0 or even higher (a 10% solution, made from a commercial grade, may have a pH of 7.4 to 7.7).

Air & Water Reactions

Water soluble. Aqueous solutions are subject to quick air oxidation at pH greater than 6.0.

Reactivity Profile

A weak base. Materials in this group are generally soluble in water. The resulting solutions contain moderate concentrations of hydroxide ions and have pH's greater than 7.0. They react as bases to neutralize acids. These neutralizations generate heat, but less or far less than is generated by neutralization of the bases in reactivity group 10 (Bases) and the neutralization of amines. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible.

Health Hazard

SYMPTOMS: Ingestion of 10 grams or more of this type of compound may cause diarrhea.

Fire Hazard

Flash point data for Sodium ascorbate are not available. Sodium ascorbate is probably combustible.

Flammability and Explosibility

Notclassified

Pharmaceutical Applications

Sodium ascorbate is used as an antioxidant in pharmaceutical formulations, and also in food products where it increases the effectiveness of sodium nitrite against growth of Listeria monocytogenes in cooked meats. It improves gel cohesiveness and sensory firmness of fiberized products regardless of vacuum treatment. It is also used therapeutically as a source of vitamin C in tablets and parenteral preparations.

Biochem/physiol Actions

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 used in a wide variety of applications, including cell culture, as a reducing agent that helps reduce oxidative stress. L-Ascorbate can be regenerated by biological systems.

Safety Profile

Human mutation data reported. When heated to decomposition it emits toxic fumes of Na2O.

Safety

The parenteral administration of 0.25-1.00 g of sodium ascorbate, given daily in divided doses, is recommended in the treatment of vitamin C deficiencies. Various adverse reactions have been reported following the administration of 1 g or more of sodium ascorbate, although ascorbic acid and sodium ascorbate are usually well tolerated; see Ascorbic acid. There have been no reports of adverse effects associated with the much lower concentrations of sodium ascorbate and ascorbic acid, which are employed as antioxidants. The WHO has set an acceptable daily intake of ascorbic acid, potassium ascorbate, and sodium ascorbate, as antioxidants in food, at up to 15 mg/kg body-weight in addition to that naturally present in food.

storage

Sodium ascorbate is relatively stable in air, although it gradually darkens on exposure to light. Aqueous solutions are unstable and subject to rapid oxidation in air at pH > 6.0. The bulk material should be stored in a well-closed nonmetallic container, protected from light, in a cool, dry place.

Incompatibilities

Incompatible with oxidizing agents, heavy metal ions, especially copper and iron, methenamine, sodium nitrite, sodium salicylate, and theobromine salicylate. The aqueous solution is reported to be incompatible with stainless steel filters.

Regulatory Status

GRAS listed. Accepted for use as a food additive in Europe. Included in the FDA Inactive Ingredients Database (IV preparations; oral tablets). Included in nonparenteral and parenteral medicines licensed in the UK. Included in the Canadian List of Acceptable Non-medicinal Ingredients.

Check Digit Verification of cas no

The CAS Registry Mumber 134-03-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,3 and 4 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 134-03:
(5*1)+(4*3)+(3*4)+(2*0)+(1*3)=32
32 % 10 = 2
So 134-03-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O6.Na/c7-1-2(8)5-3(9)4(10)6(11)12-5;/h2,5,7-10H,1H2;/q;+1/p-1

134-03-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (A0539)  Sodium L-Ascorbate  >98.0%(T)

  • 134-03-2

  • 25g

  • 112.00CNY

  • Detail
  • TCI America

  • (A0539)  Sodium L-Ascorbate  >98.0%(T)

  • 134-03-2

  • 500g

  • 432.00CNY

  • Detail
  • Alfa Aesar

  • (A17759)  L-Ascorbic acid sodium salt, 99%   

  • 134-03-2

  • 100g

  • 183.0CNY

  • Detail
  • Alfa Aesar

  • (A17759)  L-Ascorbic acid sodium salt, 99%   

  • 134-03-2

  • 500g

  • 670.0CNY

  • Detail
  • Sigma-Aldrich

  • (PHR1279)    pharmaceutical secondary standard; traceable to USP and PhEur

  • 134-03-2

  • PHR1279-1G

  • 732.19CNY

  • Detail
  • Sigma-Aldrich

  • (Y0000039)  Sodiumascorbate  European Pharmacopoeia (EP) Reference Standard

  • 134-03-2

  • Y0000039

  • 1,880.19CNY

  • Detail
  • Sigma

  • (11140)  (+)-SodiumL-ascorbate  BioXtra, ≥99.0% (NT)

  • 134-03-2

  • 11140-50G

  • 338.13CNY

  • Detail
  • Sigma

  • (11140)  (+)-SodiumL-ascorbate  BioXtra, ≥99.0% (NT)

  • 134-03-2

  • 11140-250G

  • 692.64CNY

  • Detail
  • Sigma

  • (11140)  (+)-SodiumL-ascorbate  BioXtra, ≥99.0% (NT)

  • 134-03-2

  • 11140-1KG

  • 1,979.64CNY

  • Detail
  • USP

  • (1613509)  Sodiumascorbate  United States Pharmacopeia (USP) Reference Standard

  • 134-03-2

  • 1613509-200MG

  • 4,588.74CNY

  • Detail

134-03-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Sodium L-Ascorbate

1.2 Other means of identification

Product number -
Other names Sodium ascorbate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:134-03-2 SDS

134-03-2Synthetic route

sodium ascorbate
134-03-2

sodium ascorbate

dichlorodiethylstannane
866-55-7

dichlorodiethylstannane

Sn(4+)*2C2H5(1-)*C6H6O6(2-)*H2O=Sn(C2H5)2(C6H6O6)*H2O

Sn(4+)*2C2H5(1-)*C6H6O6(2-)*H2O=Sn(C2H5)2(C6H6O6)*H2O

Conditions
ConditionsYield
In methanol (N2); dropwise addn. of the Sn-compound in MeOH to a suspension of ascorbate in MeOH with stirring at 0°C; after allowing to warm up to room temp. the mixt. is heated under reflux for 3 h; volatiles are removed in vac. and the solid is successively washed with CH2Cl2 and THF and water, recrystn. from MeOH; elem. anal.;85%
dimethyltin dichloride
753-73-1

dimethyltin dichloride

sodium ascorbate
134-03-2

sodium ascorbate

Sn(CH3)2(C6H6O6)*H2O

Sn(CH3)2(C6H6O6)*H2O

Conditions
ConditionsYield
In methanol (N2;) dropwise addn. of Sn compound in MeOH to a suspension of ascorbate in MeOH with stirring at 0°C; after allowing to warm up to room temp. the mixt. is heated under reflux for 3.5 h; volatiles are removed in vac. and the solid is successively washed with CH2Cl2 and THF, recrystn. from MeOH; elem. anal.;73%
sodium ascorbate
134-03-2

sodium ascorbate

diphenyltin(IV) dichloride
1135-99-5

diphenyltin(IV) dichloride

[Ph2Sn(L-ascorbic acid(-2H))]

[Ph2Sn(L-ascorbic acid(-2H))]

Conditions
ConditionsYield
In methanol byproducts: NaCl; (N2); soln. of Sn compd. (1 equiv.) in methanol was added dropwise with stirring to suspn. of ascorbate (2 equiv.) in methanol at 0°C; soln. was warmed to room temp.; refluxed for 3 h; filtered; concd. (vac.); washed (CH2Cl2); recrystd. (methanol); elem. anal.;50%
sodium ascorbate
134-03-2

sodium ascorbate

triphenyltin chloride
639-58-7

triphenyltin chloride

[Ph3Sn(L-ascorbate)]

[Ph3Sn(L-ascorbate)]

Conditions
ConditionsYield
In methanol byproducts: NaCl; (N2); soln. of Sn compd. (1 equiv.) in methanol was added dropwise with stirring to suspn. of ascorbate (1 equiv.) in methanol; soln. was stirred at room temp. for 10 min; refluxed for 6 h; filtered; volatiles removed (vac.); washed (CH2Cl2); dried (vac.); recrystd. (methanol); elem. anal.;47%
bis(cyclopentadienyl)titanium dichloride
1271-19-8

bis(cyclopentadienyl)titanium dichloride

sodium ascorbate
134-03-2

sodium ascorbate

{(C5H5)2Ti(C6H7O6)2}

{(C5H5)2Ti(C6H7O6)2}

Conditions
ConditionsYield
In water (N2); dropwise addn. of a soln. of ascorbate in water to a soln. of the Ti-compd. in water with stirring at 10°C, stirring of the mixt. for 2 h; allowing to warm slowly up to room temp.;; ppt. is collected by filtn., washed with cooled water and redissolved in THF, pptn. by addn. of hexane; elem. anal.;45%
tributyltin chloride
1461-22-9

tributyltin chloride

sodium ascorbate
134-03-2

sodium ascorbate

[(n-Bu)3Sn(L-ascorbate)]

[(n-Bu)3Sn(L-ascorbate)]

Conditions
ConditionsYield
In methanol byproducts: NaCl; (N2); soln. of Sn compd. (1 equiv.) in methanol was added dropwise with stirring to suspn. of ascorbate (1 equiv.) in methanol; soln. was stirred at room temp. for 10 min; refluxed for 6 h; filtered; volatiles removed (vac.); washed (CH2Cl2); dried (vac.); recrystd. (methanol); elem. anal.;23%
trimethyltin(IV)chloride
1066-45-1

trimethyltin(IV)chloride

sodium ascorbate
134-03-2

sodium ascorbate

[Me3Sn(L-ascorbate)]

[Me3Sn(L-ascorbate)]

Conditions
ConditionsYield
In methanol byproducts: NaCl; (N2); soln. of Sn compd. (1 equiv.) in methanol was added dropwise with stirring to suspn. of ascorbate (1 equiv.) in methanol; soln. was stirred at room temp. for 10 min; refluxed for 6 h; filtered; volatiles removed (vac.); washed (CH2Cl2); dried (vac.); recrystd. (methanol); elem. anal.;20%
dibutyltin chloride
683-18-1

dibutyltin chloride

sodium ascorbate
134-03-2

sodium ascorbate

[(n-Bu)2Sn(L-ascorbic acid(-2H))]

[(n-Bu)2Sn(L-ascorbic acid(-2H))]

Conditions
ConditionsYield
In methanol byproducts: NaCl; (N2); soln. of Sn compd. (1 equiv.) in methanol was added dropwise with stirring to suspn. of ascorbate (2 equiv.) in methanol at 0°C; soln. was warmed to room temp.; refluxed for 3 h; filtered; concd. (vac.); washed (CH2Cl2); recrystd. (methanol); elem. anal.;20%
sodium ascorbate
134-03-2

sodium ascorbate

tripropyltin chloride
2279-76-7

tripropyltin chloride

[(n-Pr)3Sn(L-ascorbate)]

[(n-Pr)3Sn(L-ascorbate)]

Conditions
ConditionsYield
In methanol byproducts: NaCl; (N2); soln. of Sn compd. (1 equiv.) in methanol was added dropwise with stirring to suspn. of ascorbate (1 equiv.) in methanol; soln. was stirred at room temp. for 10 min; refluxed for 6 h; filtered; volatiles removed (vac.); washed (CH2Cl2); dried (vac.); recrystd. (methanol); elem. anal.;20%
sodium ascorbate
134-03-2

sodium ascorbate

2-O-α-D-glucopyranosyl L-ascorbate
129499-78-1

2-O-α-D-glucopyranosyl L-ascorbate

Conditions
ConditionsYield
rat intestinal (or rice seed) α-glucosidase, maltose, thiourea, 0.1 M acetate buffer, 3 h, 50 deg C, in the dark;14%
sodium ascorbate
134-03-2

sodium ascorbate

alpha cyclodextrin
10016-20-3

alpha cyclodextrin

2-O-α-D-glucopyranosyl L-ascorbate
129499-78-1

2-O-α-D-glucopyranosyl L-ascorbate

Conditions
ConditionsYield
Stage #1: sodium ascorbate; alpha cyclodextrin With cyclodextrin glucanotransferase from Thermoanaerobacter sp. In aq. acetate buffer at 40℃; for 24h; pH=4.0; Enzymatic reaction;
Stage #2: With amyloglucosidase from Aspergillus niger In aq. acetate buffer at 60℃; for 2h; Enzymatic reaction; regioselective reaction;
0.27%
sodium ascorbate
134-03-2

sodium ascorbate

β‐cyclodextrin
7585-39-9

β‐cyclodextrin

2-O-α-D-glucopyranosyl L-ascorbate
129499-78-1

2-O-α-D-glucopyranosyl L-ascorbate

Conditions
ConditionsYield
Stage #1: sodium ascorbate; β‐cyclodextrin With cyclodextrin glucanotransferase from Thermoanaerobacter sp. In aq. acetate buffer at 40℃; for 24h; pH=4.0; Enzymatic reaction;
Stage #2: With amyloglucosidase from Aspergillus niger In aq. acetate buffer at 60℃; for 2h; Enzymatic reaction; regioselective reaction;
0.24%
sodium ascorbate
134-03-2

sodium ascorbate

cyclomaltooctaose
17465-86-0

cyclomaltooctaose

2-O-α-D-glucopyranosyl L-ascorbate
129499-78-1

2-O-α-D-glucopyranosyl L-ascorbate

Conditions
ConditionsYield
Stage #1: sodium ascorbate; cyclomaltooctaose With cyclodextrin glucanotransferase from Thermoanaerobacter sp. In aq. acetate buffer at 40℃; for 24h; pH=4.0; Enzymatic reaction;
Stage #2: With amyloglucosidase from Aspergillus niger In aq. acetate buffer at 60℃; for 2h; Enzymatic reaction; regioselective reaction;
0.21%
water
7732-18-5

water

sodium ascorbate
134-03-2

sodium ascorbate

oxygen

oxygen

alkaline solution

alkaline solution

A

oxalic acid
144-62-7

oxalic acid

B

L-threonic acid-4-lactone
21730-93-8

L-threonic acid-4-lactone

Conditions
ConditionsYield
Behandeln des Natrium-Salzes oder anderer Alkalisalze;
sodium metaborate
7775-19-1

sodium metaborate

sodium ascorbate
134-03-2

sodium ascorbate

3Na(1+)*{B(C6H5O6)2}(3-)*3H2O=Na3{B(C6H5O6)2}*3H2O

3Na(1+)*{B(C6H5O6)2}(3-)*3H2O=Na3{B(C6H5O6)2}*3H2O

Conditions
ConditionsYield
In not given pptg. with methanol;
In not given pptg. with methanol;
sodium ascorbate
134-03-2

sodium ascorbate

ascorbic acid
50-81-7

ascorbic acid

hydrogen
1333-74-0

hydrogen

Conditions
ConditionsYield
With tris(2,2'-bipyridyl)ruthenium dichloride; C18H23N3NiS3(2+)*2ClO4(1-) In N,N-dimethyl acetamide; water pH=4; Catalytic behavior; Irradiation;

134-03-2Related news

Assessing the use of 35 percent Sodium ascorbate (cas 134-03-2) for removal of residual hydrogen peroxide after in-office tooth bleaching10/01/2019

The authors conducted a study to quantify the amount of hydrogen peroxide remaining after in-office bleaching and to investigate the effectiveness of 35 percent sodium ascorbate (SA) on removal of the bleaching agent from dentin. The authors sectioned 70 extracted human third molars to form 4...detailed

134-03-2Relevant articles and documents

Synthesis and study of mutagenic properties of lupane triterpenoids containing 1,2,3-triazole fragments in the C-30 position

Antimonova,Petrenko,Shakirov,Rybalova,Frolova,Shul'ts,Kukina,Sinitsyna,Tolstikov

, p. 657 - 664 (2013/11/06)

New derivatives of betulin, betulinic acid methyl ester, and their acetate analogs containing 1,2,3-triazole fragments in the C-30 position were synthesized. It was shown using the Ames test that 30-azidolup-20(29)-enes and 3β,28-diacetoxy-30-(4-R-1,2,3-t

AGRICULTURAL COMPOSITION COMPRISING NITRIC OXIDE GENERATING AGENT

-

Page/Page column 5, (2008/06/13)

The invention discloses the use of a composition comprising at least one nitric oxide generating agent for increasing production of and/or retention of a plant organ.

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