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Spinetoram J

Spinetoram J structure

CAS No:
187166-40-1
Formula:
C42H69NO10
Chemical Name:
Spinetoram J
Synonyms:
1H-as-Indaceno[3,2-d]oxacyclododecin-7,15-dione,2-[(6-deoxy-3-O-ethyl-2,4-di-O-methyl-α-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)-;1H-as-Indaceno[3,2-d]oxacyclododecin-7,15-dione,2-[(6-deoxy-3-O-ethyl-2,4-di-O-methyl-α-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-(2R*,3aR*,5aR*,5bS*,9S*,13S*,14R*,16aS*,16bR*)]-;(2R,3aR,5aR,5bS,9S,13S,14R,16aS,16bR)-2-[(6-Deoxy-3-O-ethyl-2,4-di-O-methyl-α-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-1H-as-indaceno[3,2-d]oxacyclododecin-7,15-dione;DE 175J;XDE 175J
Categories:
Agrochemicals > Insecticides

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Spinetoram J Basic Attributes

Molecular Weight：

748.004

Exact Mass：

748.00

UNII：

2HRU6LA8S5

DSSTox ID：

DTXSID3052854

Characteristics

PSA：

111

XLogP3：

5.9

Density：

1.15±0.1 g/cm3(Predicted)

Boiling Point：

803.5±65.0 °C(Predicted)

Safety Information

Precautionary statement(s)：

P261, P272, P280, P302+P352, P321, P333+P313, P363, P501

Hazard Statements：

H317

GHS Classification：

|Warning|H317 (100%): May cause an allergic skin reaction [Warning Sensitization, Skin]|P261, P272, P280, P302+P352, P321, P333+P313, P363, and P501|Aggregated GHS information provided by 39 companies from 1 notifications to the ECHA C&L Inventory.

Spinetoram J Use and Manufacturing

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.

Use Classification：

Transformation products

Computed Properties

Molecular Weight:748.0
XLogP3:5.9
Hydrogen Bond Acceptor Count:11
Rotatable Bond Count:10
Exact Mass:747.49214740
Monoisotopic Mass:747.49214740
Topological Polar Surface Area:111
Heavy Atom Count:53
Complexity:1260
Defined Atom Stereocenter Count:17
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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SPINETORAM

CAS No.: 187166-40-1

Content: 99.00%

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