An internal standard for the quantification of fumonisin B3
Related Products
Isomer(s)
31273Fumonisin B2-13C34
Unlabeled Version(s)
20434Fumonisin B3
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Fumonisin B3-13C34

Item No. 31274

Technical Information
Formal Name
(2R,2'R)-2,2'-((((5R,6R,7S,9S,11R,18S,19S)-19-amino-11,18-dihydroxy-5,9-di(methyl-13C)icosane-6,7-diyl-1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20-13C20)bis(oxy))bis(2-oxoethane-2,1-diyl-1,2-13C2))disuccinic-13C4 acid
Synonyms
  • FB3-13C34
Molecular Formula
[13C]34H59NO14
Formula Weight
Purity
≥95%
Formulation
A 10 µg/ml 1:1 solution in acetonitrile:water
Acetone:Water (1:1): soluble
SMILES
O=[13C](O[13C@@H]([13CH2][13C@H]([13CH2][13C@@H]([13CH2][13CH2][13CH2][13CH2][13CH2][13CH2][13C@@H]([13C@H]([13CH3])N)O)O)[13CH3])[13C@@H]([13C@H]([13CH3])[13CH2][13CH2][13CH2][13CH3])O[13C]([13CH2][13C@H]([13C](O)=O)[13CH2][13C](O)=O)=O)[13CH2][13C@H]([13C](O)=O)[13CH2][13C](O)=O
InChi Code
InChI=1S/C34H59NO14/c1-5-6-11-21(3)32(49-31(43)19-24(34(46)47)17-29(40)41)27(48-30(42)18-23(33(44)45)16-28(38)39)15-20(2)14-25(36)12-9-7-8-10-13-26(37)22(4)35/h20-27,32,36-37H,5-19,35H2,1-4H3,(H,38,39)(H,40,41)(H,44,45)(H,46,47)/t20-,21+,22-,23+,24+,25+,26-,27-,32+/m0/s1/i1+1,2+1,3+1,4+1,5+1,6+1,7+1,8+1,9+1,10+1,11+1,12+1,13+1,14+1,15+1,16+1,17+1,18+1,19+1,20+1,21+1,22+1,23+1,24+1,25+1,26+1,27+1,28+1,29+1,30+1,31+1,32+1,33+1,34+1
InChi Key
CPCRJSQNWHCGOP-BMUNAYDHSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    Fumonisin B3-13C34 (FB3-13C34) is intended for use as an internal standard for the quantification of fumonisin B3 (Item No. 20434) by GC- or LC-MS. FB3 is a mycotoxin that has been found in Fusarium.1 It is cytotoxic to primary rat hepatocytes when used at concentrations of 125, 250, and 500 µM.2 Dietary administration of FB3 (0.05%) for 14 or 21 days induces hepatocyte nodules, a marker of cancer initiation, in rats.2 FB3 has been detected in corn and corn-based foods and livestock feeds.3

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Rheeder, J.P., Marasas, W.F.O., and Vismer, H.F. Production of fumonisin analogs by Fusarium species. Appl. Environ. Microbiol. 68(5), 2101-2105 (2002).

    2. Gelderblom, W.C.A., Cawood, M.E., Snyman, S.D., et alStructure-activity relationships of fumonisins in short-term carcinogenesis and cytotoxicity assays. Food Chem. Toxicol. 31(6), 407-414 (1993).

    3. Bullerman, L.B. Occurrence of Fusarium and fumonisins on food grains and in foods. Fumonisins in food 27-38 (1996).