A degradation product of spinosyn J
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3'-Ethoxy-5,6-dihydro Spinosyn J 17-pseudoaglycone

Item No. 25765

Product Insert (PDF)Safety Data Sheet (SDS) (PDF)
Technical Information
Formal Name
2-[(6-deoxy-3-O-ethyl-2,4-di-O-methyl-α-L-mannopyranosyl)oxy]-9-ethyl-2R,3,3aR,4,5,5aR,5bS,6,9S,10,11,12,13S,14R,16aS,16bR-hexadecahydro-13-hydroxy-14-methyl-1H-as-indaceno[3,2-d]oxacyclododecin-7,15-dione
CAS Number
2055494-09-0
Molecular Formula
C34H54O9
Formula Weight
606.8
Purity
≥95%
Formulation
A solid
SMILES
O=C1C2=C[C@]3([H])[C@](CC[C@@]4([H])[C@@]3([H])C[C@H](O[C@]5([H])O[C@@H](C)[C@H](OC)[C@@H](OCC)[C@H]5OC)C4)([H])[C@]2([H])CC(O[C@@H](CC)CCC[C@H](O)[C@H]1C)=O
InChi Code
InChI=1S/C34H54O9/c1-7-21-10-9-11-28(35)18(3)30(37)27-16-25-23(26(27)17-29(36)42-21)13-12-20-14-22(15-24(20)25)43-34-33(39-6)32(40-8-2)31(38-5)19(4)41-34/h16,18-26,28,31-35H,7-15,17H2,1-6H3/t18-,19+,20-,21+,22-,23-,24-,25-,26+,28+,31+,32-,33-,34+/m1/s1
InChi Key
XQMXNJMHUPATAK-WGUIIDCHSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Wet ice in continental US; may vary elsewhere
Certificates of Analysis & Batch Specific Data

Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

    1 mg

    $303

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    5 mg

    $1,060

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    Cayman Chemical
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    Product Description

    3'-Ethoxy-5,6-dihydro spinosyn J 17-pseudoaglycone is a degradation product of 3’-ethoxy-5,6-dihydro spinosyn J, a component of the insecticide spinosyn J.1,2 It has no insecticidal activity against the tobacco budworm up to a concentration of 64 ppm.2

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Kirst, H.A. The spinosyn family of insecticides: Realizing the potential of natural products research. J. Antibiot. (Tokyo) 63(3), 101-111 (2010).

    2. Creemer, L.C., Kirst, H.A., and Paschal, J.W. Conversion of spinosyn A and spinosyn D to their respective 9- and 17-pseudoaglycones and their aglycones. J. Antibiot. (Tokyo) 51(8), 795-800 (1998).