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Sodium ascorbate - for cell culture，≥99.0%, high purity , CAS No.134-03-2

for cell culture
≥99%

CAS#: 134-03-2
Formula: C₆H₇NaO₆
Molecular Weight: 198.11
Beilstein Registry Number: 3767246
EC Number: 205-126-1
MDL number: MFCD00082340
PubChem CID: 23667548

Item Number

S105026

Grouped product items
SKU	Size	Availability	Price	Qty
S105026-100g	100g	In stock	$42.90
S105026-500g	500g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$167.90

View related series

Imidazoles Ionic liquid

Basic Description

Synonyms	SODIUM ASCORBATE\|134-03-2\|Sodium L-ascorbate\|L-Ascorbic acid sodium salt\|Vitamin C sodium\|Monosodium L-ascorbate\|Ascorbicin\|Ascorbic acid sodium salt\|Natrii ascorbas\|Vitamin C Sodium Salt\|Iskia-C\|Natri-C\|Ascorbate de sodium\|Sodascorbate\|(+)-Sodium L-ascor
Specifications & Purity	for cell culture, ≥99%
Storage Temp	Argon charged
Shipped In	Normal
Grade	for cell culture
Product Description	Sodium ascorbate is a potential antioxidant and is a derivative of vitamin C (L-ascorbic acid).[1][2] It is widely used as a food additive.[1] In addition, SA enhances growth retardation activity of bleomycin sulfate, R020-1724 (an inhibitor of cyclic nucleotide phosphodiesterase), prostaglandin E1 and sodium butyrate agents on neuroblastoma cells in culture.[3] Elevated levels of SA induces two-stage urinary bladder carcinogenesis in rats.[1] sodium L-ascorbate in combination with collagenogenesis inhibitors is used to treat dermal scars and keloids. Application： Sodium ascorbate has been used: · to produce H2O2 in cell culture media; · as a reducing agent for a cell-permeable artificial electron donor, N,N,N′,N′-tetramethyl-p-phenylenediamine (TMPD); · to study its effect on production of collagen and elastic fibers in fibroblasts cultures derived from normal human skin and dermal fat.

Associated Targets

CRYAB Tchem Alpha-crystallin B chain 0 Activities

Discover Target: CRYAB

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

FFAR3 Tchem Free fatty acid receptor 3 0 Activities

Discover Target: FFAR3

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

Names and Identifiers

IUPAC Name	sodium;(2R)-2-[(1S)-1,2-dihydroxyethyl]-4-hydroxy-5-oxo-2H-furan-3-olate
INCHI	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
InChi Key	PPASLZSBLFJQEF-RXSVEWSESA-M
Canonical SMILES	[Na+].OC[C@H](O)[C@H]1OC(=O)C(O)=C1[O-]
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

Certificates

Certificate of Analysis(COA)

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4 results found

Lot Number	Certificate Type	Date	Item
B2308411	Certificate of Analysis	Dec 23, 2021	S105026
C2204642	Certificate of Analysis	Dec 23, 2021	S105026
C2204643	Certificate of Analysis	Dec 23, 2021	S105026
H2412485	Certificate of Analysis	Dec 23, 2021	S105026

Chemical and Physical Properties

Solubility	Soluble in water. Slightly soluble in alcohol. Insoluble in chloroform and ether.
Sensitivity	Light & Moisture sensitive
Specific Rotation[α]	105.5 ° (C=10, H2O)
Melt Point(°C)	219-221°C

Safety and Hazards(GHS)

WGK Germany	1
RTECS	CI7671000

Alternative Products

References

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