Sodium ascorbate (Synonyms: Sodium L-ascorbate; Vitamin C sodium salt) |
|
Catalog No.GC13616
|
Sodium ascorbate is an endogenous antioxidant that participates in hydroxylation reactions in the body, promotes the formation of intercellular substances, assists in corticosteroid synthesis, and influences blood cell maturation by promoting folic acid reduction and iron ion absorption. Sodium ascorbate also possesses antihistaminic effects and inhibits the formation of nitrosamines.
Products are for research use only. Not for human use. We do not sell to patients.
Cas No.: 134-03-2
Sample solution is provided at 25 µL, 10mM.
Sodium ascorbate is an endogenous antioxidant that participates in hydroxylation reactions in the body, promotes the formation of intercellular substances, assists in corticosteroid synthesis, and influences blood cell maturation by promoting folic acid reduction and iron ion absorption. Sodium ascorbate also possesses antihistaminic effects and inhibits the formation of nitrosamines[1-2]. Sodium ascorbate can be used for the prevention and treatment of scurvy, infectious diseases, acute attacks of Keshan disease, liver diseases, as well as adjuvant therapy for various anemias, allergic skin diseases, and cancer [3-4].
In vitro, Sodium ascorbate (10µM) treatment of B16 murine melanoma cells for 4 hours, Sodium ascorbate significantly induced apoptosis and downregulated transferrin receptor (TfR) expression, thereby reducing intracellular iron levels dependent on iron uptake[5]. Sodium ascorbate (0.5–3mM) treatment of human neuroblastoma cells (e.g., HTLA-230, SH-SY5Y) for 24 hours, Sodium ascorbate significantly induced caspase-dependent apoptosis, accompanied by loss of mitochondrial membrane potential, reduced cell proliferation, and decreased glycolytic capacity[6].
In vivo, Sodium ascorbate (60mg/kg) subcutaneously administered to tumor-bearing mice (P388 leukemia cells) (daily dosing starting from the first day after tumor implantation and continuing for 16 days), Sodium ascorbate significantly reduced tumor volume and weight, and improved mouse survival[7]. Sodium ascorbate (5mg/mouse) intraperitoneally administered to autoimmune arthritis mice (every other day for 21 days starting from the first day after immunization), Sodium ascorbate significantly delayed arthritis onset, reduced disease severity, and decreased autoantibody production[8].
References:
[1] Carr AC, Maggini S. Vitamin C and Immune Function. Nutrients. 2017 Nov 3;9(11):1211. doi: 10.3390/nu9111211.
[2] Padayatty SJ, Levine M. Vitamin C: the known and the unknown and Goldilocks. Oral Dis. 2016 Sep;22(6):463-93.
[3] Gęgotek A, Skrzydlewska E. Ascorbic acid as antioxidant. Vitam Horm. 2023;121:247-270.
[4] Moores J. Vitamin C: a wound healing perspective. Br J Community Nurs. 2013 Dec;Suppl:S6, S8-11.
[5] Kang JS, Cho D, Kim YI, et al. Sodium ascorbate (vitamin C) induces apoptosis in melanoma cells via the down-regulation of transferrin receptor dependent iron uptake. J Cell Physiol. 2005 Jul;204(1):192-7.
[6] Carosio R, Zuccari G, Orienti I, et al. Sodium ascorbate induces apoptosis in neuroblastoma cell lines by interfering with iron uptake. Mol Cancer. 2007 Aug 30;6:55.
[7] Osswald H, Herrmann R, Youssef M. The influence of sodium ascorbate, menadione sodium bisulfite or pyridoxal hydrochloride on the toxic and antineoplastic action of N-methylformamide in P 388 leukemia or M 5076 sarcoma in mice. Toxicology. 1987 Feb;43(2):183-91.
[8] Yin Y, Wu S. Ascorbic acid alleviates rheumatoid arthritis by inhibiting the production of autoantibodies. Cell Commun Signal. 2024 Jul 24;22(1):373.
| Cell experiment [1]: | |
|
Cell lines |
Human neuroblastoma cell lines (HTLA-230, IMR-32, LAN-5, GI-LI-N, SH-SY5Y) |
|
Preparation Method |
Cells were maintained in Dulbecco’s modified Eagle medium (DMEM) supplemented with 10% fetal bovine serum (FBS), 2mM L-glutamine, and antibiotics at 37°C, 5% CO₂. Cells were treated with Sodium Ascorbate at concentrations ranging from 0.5mM to 3mM for 6–24 hours. |
|
Reaction Conditions |
0.5–3mM; 6–24h |
|
Applications |
Sodium Ascorbate induced dose- and time-dependent apoptosis in all neuroblastoma cell lines, characterized by an increase in sub-G1 phase cells and caspase activation. Sodium Ascorbate significantly downregulated transferrin receptor (TfR/CD71) expression, leading to reduced intracellular iron levels. Treatment with Sodium Ascorbate also caused early loss of mitochondrial membrane potential (ΔΨm), and these effects were reversible by the iron donor ferric ammonium citrate (FAC), confirming iron depletion as the key mechanism of apoptosis. |
| Animal experiment [2]: | |
|
Animal models |
C57BL/6 mice with collagen-induced arthritis (CIA) or lupus-like autoimmune disease (bm12-induced model) |
|
Preparation Method |
Mice were intraperitoneally injected with Sodium Ascorbate (5mg/mouse, dissolved in PBS) every other day for 7–21 days. For CIA, immunization with chicken type II collagen (CII) was performed 1 day after the first Sodium Ascorbate injection. For antibody response studies, mice were immunized with NP-Ficoll (T-independent) or NP-KLH (T-dependent) antigens. |
|
Dosage form |
5mg/mouse; i.p.; intermittent injection (every 48h). |
|
Applications |
Sodium Ascorbate significantly delayed arthritis onset and reduced disease severity in CIA mice, as evidenced by decreased clinical scores, synovial inflammation, cartilage/bone damage, and osteoclast activity. Sodium Ascorbate also suppressed autoantibody production (e.g., collagen-specific IgG and rheumatoid factor) in both arthritis and lupus models. Mechanistically, ascorbic acid inhibited B cell differentiation into plasma cells, disrupted germinal center formation, and impaired antibody affinity maturation by blocking STAT3 signaling and promoting B cell apoptosis. |
|
References: |
|
| Cas No. | 134-03-2 | SDF | |
| Synonyms | Sodium L-ascorbate; Vitamin C sodium salt | ||
| Chemical Name | sodium (R)-2-((S)-1,2-dihydroxyethyl)-4-hydroxy-5-oxo-2,5-dihydrofuran-3-olate | ||
| Canonical SMILES | O=C1C(O)=C([O-])[C@@H]([C@@H](O)CO)O1.[Na+] | ||
| Formula | C6H7NaO6 | M.Wt | 198.11 |
| Solubility | ≥ 9.1mg/mL in Water | Storage | 4°C, protect from light |
| General tips | Please select the appropriate solvent to prepare the stock solution according to the
solubility of the product in different solvents; once the solution is prepared, please store it in
separate packages to avoid product failure caused by repeated freezing and thawing.Storage method
and period of the stock solution: When stored at -80°C, please use it within 6 months; when stored
at -20°C, please use it within 1 month. To increase solubility, heat the tube to 37°C and then oscillate in an ultrasonic bath for some time. |
||
| Shipping Condition | Evaluation sample solution: shipped with blue ice. All other sizes available: with RT, or with Blue Ice upon request. | ||
| Prepare stock solution | |||
|
1 mg | 5 mg | 10 mg |
| 1 mM | 5.0477 mL | 25.2385 mL | 50.477 mL |
| 5 mM | 1.0095 mL | 5.0477 mL | 10.0954 mL |
| 10 mM | 504.8 μL | 2.5239 mL | 5.0477 mL |
Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)
Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)
Calculation results:
Working concentration: mg/ml;
Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )
Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL saline, mix and clarify.
Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.
Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such as vortex, ultrasound or hot water bath can be used to aid dissolving.
3. All of the above co-solvents are available for purchase on the GlpBio website.
Quality Control & SDS
- View current batch:
- Purity: >99.00% Appearance: A solid
- COA (Certificate of Analysis)
- SDS (Safety Data Sheet)
- Datasheet
Average Rating: 5 (Based on Reviews and 9 reference(s) in Google Scholar.)















