A vitamin produced in fungi and invertebrates
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Vitamin D2

Item No. 11791

Technical Information
Formal Name
(1S)-4-methylene-3Z-[2E-[(1R,3aS,7aR)-octahydro-7a-methyl-1-[(1R,2E,4R)-1,4,5-trimethyl-2-hexen-1-yl]-4H-inden-4-ylidene]ethylidene]-cyclohexanol
CAS Number
50-14-6
Synonyms
  • Calciferol
  • Ergocalciferol
  • Fortodyl
  • Infron
  • Mulsiferol
  • NSC 62792
  • Radiostol
  • Uvesterol D
Molecular Formula
C28H44O
Formula Weight
Purity
≥98%
A crystalline solid
DMF: 20 mg/mlDMSO: 2 mg/mlEthanol: 20 mg/ml
λmax
212, 265 nm
SMILES
C=C1CC[C@H](O)C/C1=C/C=C2[C@@](CC[C@@]3([C@H](C)/C=C/[C@H](C)C(C)C)[H])([H])[C@]3(C)CCC/2
InChi Code
InChI=1S/C28H44O/c1-19(2)20(3)9-10-22(5)26-15-16-27-23(8-7-17-28(26,27)6)12-13-24-18-25(29)14-11-21(24)4/h9-10,12-13,19-20,22,25-27,29H,4,7-8,11,14-18H2,1-3,5-6H3/b10-9+,23-12+,24-13-/t20-,22+,25-,26+,27-,28+/m0/s1
InChi Key
MECHNRXZTMCUDQ-RKHKHRCZSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Vitamin D2 is produced in fungi, including yeast, and invertebrates from ergosterol in response to ultraviolet radiation. In vertebrates as well as host organisms, vitamin D2 is metabolized first to 25-hydroxyvitamin D2 and subsequently to the active 1,25-dihydroxyvitamin D2.1,2 Differences in the metabolism and action of vitamin D2 vs. vitamin D3 in mammals is a current topic of research interest.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Holick, M.F. Vitamin D deficiency. N. Engl. J. Med. 357(3), 266-281 (2007).

    2. Houghton, L.A., and Vieth, R. The case against ergocalciferol (vitamin D2) as a vitamin supplement. Am. J. Clin. Nutr. 84(4), 694-697 (2006).