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A0278

L-Ascorbic acid

reagent grade

Synonym(s):

L-Threoascorbic acid, Antiscorbutic factor, Vitamin C

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About This Item

Empirical Formula (Hill Notation):
C6H8O6
CAS Number:
50-81-7
Molecular Weight:
176.12
UNSPSC Code:
12352209
NACRES:
NA.26
PubChem Substance ID:
24890417
EC Number:
200-066-2
Beilstein/REAXYS Number:
84272
MDL number:
MFCD00064328
Assay:
≥98% (with Iodine, titration)
Form:
powder
Grade:
reagent grade
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biological source

synthetic

Quality Level

200

grade

reagent grade

assay

≥98% (with Iodine, titration)

form

powder

technique(s)

HPLC: suitable

color

white to light yellow

pH

1.0-2.5 (25 °C, 176 g/L in water)

mp

190-194 °C (dec.)

solubility

water: soluble 50 mg/mL

SMILES string

OC([C@]([C@@H](O)CO)([H])O1)=C(O)C1=O

InChI

1S/C6H8O6/c7-1-2(8)5-3(9)4(10)6(11)12-5/h2,5,7-10H,1H2/t2-,5+/m0/s1

InChI key

CIWBSHSKHKDKBQ-JLAZNSOCSA-N

Gene Information

human ... SLC23A2(9962)

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General description

Ascorbic Acid, also known as Vitamin C, is a six-carbon lactone produced by plants and some animal species but not by humans and other primates. It is a water-soluble vitamin.

Application

L-Ascorbic acid has been used as a standard in high performance liquid chromatography (HPLC) for quantification of L-ascorbic acid.
L-Ascorbic acid may be used as standard in assay for erythrocyte hemolysis mediated by peroxyl free radicals. It may be used for the reduction of graphene oxide sheets.

Biochem/physiol Actions

L-Ascorbic acid is an anti-oxidant. L-Ascorbic acid (vitamin C) is important for many enzymatic reactions for maintaining prosthetic metal ions in their reduced forms (for example, Fe2+, Cu+). It protects tissues from oxidative damage by scavenging free radicals. It has mild reductive ability and nontoxic property. It is commonly employed reductant in the laboratory. Colorimetric determination of ascorbic acid in plasma using acid phosphotungstate has been reported.
L-ascorbic acid modified poly(ester urethane)s might facilitate soft tissue regeneration. It also helps in increasing iron absorption by tissues. In addition, it aids in tyrosine metabolism and microsomal drug metabolism.

Disclaimer

May darken in storage.

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF8619V
0000508853
0000508841
0000508841
0000508853

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Gemma Rush et al.
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Dehydrofreezing of pineapple
Ramallo LA and Mascheroni RH
Journal of Food Engineering, 99(3), 269-275 (2010)
Synthesis and characterization of cycloaliphatic hydrophilic polyurethanes, modified with L-ascorbic acid, as materials for soft tissue regeneration
Kucinska-Lipka J, et al.
Materials Science & Engineering. C, Materials For Biological Applications, 75(3), 671-681 (2017)
Solubilities of magnesium-l-ascorbate, calcium-l-ascorbate, magnesium-l-glutamate, magnesium-d-gluconate, calcium-d-gluconate, calcium-d-heptagluconate, l-aspartic acid, and 3-nitrobenzoic acid in water
Mishelevich A and Apelblat A
The Journal of Chemical Thermodynamics, 40(5), 897-900 (2008)
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Global Trade Item Number

SKUGTIN
A0278-1KG04061833327272
A0278-500G04061833327296
A0278-100G04061833327265
A0278-25G04061833327289

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