(+)-Iron(II) L-ascorbate
(+)-Iron(II) L-ascorbate, identified by CAS 24808-52-4 and with the formula C12H14FeO12, has a molecular weight of 406.08. This dark brown crystalline compound is primarily utilised in cell biology and nutrition research. As a reliable source of iron and vitamin C, it plays a role in various biochemical studies requiring these essential components.
- IUPAC
- L-(+)-Ascorbic acid iron(II) salt,Ferrous ascorbate,Vitamin C iron(II) salt
- Synonyms
- L-(+)-Ascorbic acid iron(II) saltFerrous ascorbateVitamin C iron(II) salt

Cell Biology Research
(+)-Iron(II) L-ascorbate is employed in cell culture studies to investigate cellular processes involving iron and vitamin C. Its specific chemical form allows for controlled introduction of these elements into biological systems.
Nutrition Research
This compound serves as a valuable reagent in nutrition research, enabling scientists to study the metabolic pathways and physiological effects of iron and ascorbic acid. It provides a stable source for experimental models.
Biochemical Assays
Utilised in various biochemical assays, (+)-Iron(II) L-ascorbate can act as a cofactor or reactant in enzyme-mediated reactions. Its defined composition ensures reproducibility in experimental outcomes.
| Molecular weight | 406.08 |
|---|---|
| Empirical formula | C12H14FeO12 |
| Assay | ≥90% (titration) |
| Form | crystalline |
| Colour | dark brown |
| Protective equipment | Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter |
|---|---|
| Water hazard class (WGK, DE) | 3 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is (+)-Iron(II) L-ascorbate used for?
+
(+)-Iron(II) L-ascorbate is used in cell biology and nutrition research due to its role as a source of both iron and vitamin C.
What is the CAS number and formula for (+)-Iron(II) L-ascorbate?
+
The CAS number is 24808-52-4 and the empirical formula (Hill notation) is C12H14FeO12.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies (+)-Iron(II) L-ascorbate with an assay of ≥90% (titration). This is a research grade material and TSS does not represent it as USP, BP, or EP grade.
What are the safety considerations when handling (+)-Iron(II) L-ascorbate?
+
Handle with care using appropriate personal protective equipment, including eyeshields and gloves. A type N95 (US) or type P1 (EN143) respirator filter may be necessary. It has a WGK Germany rating of 3.
How is (+)-Iron(II) L-ascorbate packed, shipped, and exported?
+
Chemicals are packed according to international safety standards for transport. Tech Serve Solutions has extensive experience in exporting fine chemicals globally.
How can I request a sample or quote for (+)-Iron(II) L-ascorbate?
+
Please use the contact form on our website or contact our sales team directly to request a sample or a quotation for (+)-Iron(II) L-ascorbate.
▶ Related products

(−)-Curcumol
C15H24O2
Cell Biology
(±) Clopidogrel hydrogensulfate
Cell Biology

(±)-L-Alliin
C6H11NO3S
Cell Biology
(±)-2-Amino-4-phosphonobutyric acid
C4H10NO5P
Cell Biology
(±)-2-Methylarachidonoyl-2′-fluoroethylamide
C23H38NOF
Cell Biology
(±)-3,4-Methylenedioxy-N-ethylamphetamine hydrochloride
Cell Biology

(±)-3,4-Methylenedioxyamphetamine hydrochloride
Cell Biology

(±)-3,4-Methylenedioxymethamphetamine hydrochloride
Cell Biology
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis