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for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Nivalenol - 13 C 15 is the 13 C labeled Nivalenol. Nivalenol , classified as type B trichotecenes toxins produced by Fusarium graminearum , is a fungal metabolite present in agricultural product. Nivalenol induces cell death through caspase -dependent mechanisms and via the intrinsic apoptotic pathway. Nivalenol affects the immune system, causes emesis, growth retardation, reproductive disorders and has a haematotoxic/myelotoxic effect.
| Canonical Smiles | CC1=CC2C(C(C1=O)O)(C3(C(C(C(C34CO4)O2)O)O)C)CO |
|---|---|
| IUPAC Name | (1'S,2S,2'R,3'S,7'R,9'R,10'R,11'S)-3',10',11'-trihydroxy-2'-(hydroxy(113C)methyl)-1',5'-di((113C)methyl)spiro[(2,3-13C2)oxirane-2,12'-8-oxatricyclo[7.2.1.02,7]dodec-5-ene]-4'-one |
| InChIKey | UKOTXHQERFPCBU-WFPUMLOVSA-N |
| INCHI | 1S/C15H20O7/c1-6-3-7-14(4-16,11(20)8(6)17)13(2)10(19)9(18)12(22-7)15(13)5-21-15/h3,7,9-12,16,18-20H,4-5H2,1-2H3/t7-,9-,10-,11-,12-,13-,14-,15+/m1/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 |
| Isomeric SMILES | [13CH3][13C]1=[13CH][13C@@H]2[13C@]([13C@@H]([13C]1=O)O)([13C@]3([13C@@H]([13C@H]([13C@H]([13C@@]34[13CH2]O4)O2)O)O)[13CH3])[13CH2]O |
| Alternate CAS | 23282-20-4 |
| PubChem CID | 117065052 |
| Molecular Weight | 327.20 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →| 1. Lakshani Madushika, Yongming Huang, Menghan Sun, Yuxuan Liu, Linfang Lu, Xiaoli Li, Na Li, Kang Jiang, Sumei Ling, Shihua Wang. (2025) Development of sensitive and rapid immunoassays for Moniliformin (MON) detection based on nanomaterials labeled monoclonal antibodies. FOOD CHEMISTRY, [PMID:39842210] [10.1016/j.foodchem.2025.142911] |