SPINETORAM Chemical Properties

Boiling point:

803.5±65.0 °C(Predicted)

Density 

1.15±0.1 g/cm3(Predicted)

solubility 

Chloroform (Slightly), Methanol (Slightly)

form 

Solid

pka

8.62±0.60(Predicted)

color 

White to Pale Yellow

InChI

InChI=1/C42H69NO10/c1-10-27-13-12-14-35(53-37-18-17-34(43(6)7)24(4)49-37)23(3)38(45)33-21-31-29(32(33)22-36(44)51-27)16-15-26-19-28(20-30(26)31)52-42-41(47-9)40(48-11-2)39(46-8)25(5)50-42/h21,23-32,34-35,37,39-42H,10-20,22H2,1-9H3/t23-,24-,25+,26-,27+,28-,29-,30-,31-,32+,34+,35+,37+,39+,40-,41-,42+/s3

InChIKey

GOENIMGKWNZVDA-PAHYXNTPNA-N

SMILES

[C@]12(C[C@@H](C[C@]1(CC[C@]1([C@]3([H])CC(=O)O[C@@H](CC)CCC[C@H](O[C@H]4CC[C@H](N(C)C)[C@@H](C)O4)[C@@H](C)C(=O)C3=C[C@@]21[H])[H])[H])O[C@H]1[C@H](OC)[C@H](OCC)[C@@H](OC)[C@H](C)O1)[H] |&1:0,2,4,7,8,14,20,22,25,29,32,38,43,44,47,51,54,r|

EPA Substance Registry System

1H-as-Indaceno[3,2-d]oxacyclododecin-7,15-dione, 2-[(6-deoxy-3-O-ethyl-2,4-di-O-methyl-.alpha.-L-mannopyranosyl)oxy]-13-[[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,4,5,5a,5b,6,9,10,11,12,13,14,16a,16b-hexadecahydro-14-methyl-, (2R,3aR,5aR,5bS,9S,13S,14R,16aS,16bR)- (187166-40-1)

SPINETORAM Usage And Synthesis

Uses

3'-Ethoxy-5,6-dihydrospinosyn J is the major component in the second generation spinosyn family of bio-insecticides marketed as Spinetoram. 3'-Ethoxy-5,6-dihydrospinosyn J is a semi-synthetic compound prepared by selective ethylation and hydrogenation of Spinosyn J, itself a fermentation product from a biosynthetically blocked mutant of Saccharopolyspora spinosa. As an insecticide, 3'-ethoxy-5,6-dihydrospinosyn J is considered more potent, and to have earlier onset and longer duration of action than combinations of spinosyn A and D.

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