Spinosad D
Spinosad D Basic information
- Product Name:
- Spinosad D
- Synonyms:
-
- 1H-as-Indaceno3,2-doxacyclododecin-7,15-dione, 2-(6-deoxy-2,3,4-tri-O-methyl-.alpha.-L-mannopyranosyl)oxy-13-(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yloxy-9-ethyl-2,3,3a,5a,5b,6,9,10,11,12,13,14,16a,16b-tetradecahydro-4,14-dimethyl-, (2
- Conserve
- DE 105
- Naturalyte
- Spinoace
- Spinosyn
- Spintor
- Success
- CAS:
- 131929-63-0
- MF:
- C42H67NO10
- MW:
- 745.982
- EINECS:
- 620-162-1
- Mol File:
- 131929-63-0.mol
Spinosad D Chemical Properties
- Melting point:
- 169°
- alpha
- 27436 -297.5° (methanol)
- Boiling point:
- 807.4±65.0 °C(Predicted)
- Density
- 1.15±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- DMF: Soluble; DMSO: Soluble; Ethanol: Soluble; Methanol: Soluble
- form
- A solid
- pka
- 7.8(at 25℃)
- color
- White to off-white
- InChI
- InChI=1/C42H67NO10/c1-11-26-13-12-14-35(53-37-16-15-34(43(6)7)24(4)49-37)23(3)38(45)33-20-31-29(32(33)21-36(44)51-26)17-22(2)28-18-27(19-30(28)31)52-42-41(48-10)40(47-9)39(46-8)25(5)50-42/h17,20,23-32,34-35,37,39-42H,11-16,18-19,21H2,1-10H3/t23-,24-,25+,26+,27-,28+,29-,30-,31-,32+,34+,35+,37+,39+,40-,41-,42+/s3
- InChIKey
- RDECBWLKMPEKPM-UAOLJFDJNA-N
- SMILES
- [C@@H]1(N(C)C)[C@@H](C)O[C@@]([H])(O[C@@H]2[C@@H](C)C(=O)C3=C[C@@]4([H])[C@]5([H])C[C@H](O[C@@]6([H])[C@H](OC)[C@H](OC)[C@@H](OC)[C@H](C)O6)C[C@@]5([H])C(C)=C[C@@]4([H])[C@]3([H])CC(=O)O[C@@H](CC)CCC2)CC1 |&1:0,4,7,10,11,17,19,22,24,26,29,32,35,39,44,46,52,r|
- EPA Substance Registry System
- Spinosyn D (131929-63-0)
Spinosad D Usage And Synthesis
Chemical Properties
Light gray-white solid crystal, with a slight stale earthy odor. Vapor pressure is about 1.3×10-10 Pa. In pH 7.74 aqueous solution, it is relatively stable to metals and metal ions within 28d. In the soil photodegradation half-life of 9 ~ 10d; water photolysis half-life <1d. In the pH value of 5 ~ 7 range, in aqueous solution is relatively stable; in the pH value of 9 when the half-life of >200d. Multi-bactericides is a mixture containing more than ten components, the main components are A and D. Spinosyn A melting point of 84 ~ 99.5 ° C, vapour pressure of 3.2 × 10-10Pa The solubility in water was 290mg/L (pH=5.0), 235mg/L (pH=7.0), 16mg/L (pH=9.0); the partition coefficients were 2.8, 4.0, 5.2 under the corresponding pH conditions, respectively.The melting point of polymicrobialin D was 161.5~170°C, and the vapour pressure was 2.1×10-10 Pa. The solubility in water was 29mg/L (pH=7.0), 4.0, 5.2, respectively. The solubility in water was 29mg/L (pH=5.0), 0.332mg/L (pH=7.0), 0.053mg/L (pH=90.0), and the partition coefficients were 3.2, 4.5, and 5.2 under the corresponding pH conditions.
Uses
Spinosyn D is the second most abundant component (comprising up to 15%) of the spinosyn fermentation complex of macrocyclic lactones. Spinosyn D is a more hydrophobic analogue, and is a potent insecticide for crop pathogens and ectoparasite control on animals, albeit less active than spinosyn A. The spinosyns have a unique mechanism of action involving disruption of nicotinic acetylcholine receptors.
Definition
ChEBI: A spinosyn in which the sugar amino and hydroxy groups are globally methylated with an additional methyl substituent attached to the tetracyclic skeleton. One of the two active ingredients of spinosad.
Spinosad D Preparation Products And Raw materials
Raw materials
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