CAS 131929-60-7
:Espinosina A
Descripción:
Espinosina A es un insecticida de origen natural derivado de la fermentación de la bacteria del suelo Saccharopolyspora spinosa. Pertenece a la clase de compuestos conocidos como espinosad, que se caracterizan por su estructura única que presenta un sistema de anillo tetracíclico. Espinosina A exhibe un amplio espectro de actividad insecticida, particularmente contra plagas lepidópteras, lo que lo hace valioso en aplicaciones agrícolas. Funciona al interrumpir el funcionamiento normal del sistema nervioso del insecto, lo que lleva a la parálisis y la muerte. El compuesto es conocido por su baja toxicidad para los mamíferos y los insectos beneficiosos, lo que lo convierte en una alternativa ecológica a los pesticidas sintéticos. Espinosina A también es estable bajo diversas condiciones ambientales, lo que contribuye a su efectividad en el manejo de plagas. Su uso está regulado en muchos países y a menudo se encuentra en formulaciones para la agricultura orgánica. En general, Espinosina A es reconocido por su eficacia, perfil de seguridad y mínimo impacto en organismos no objetivo, alineándose con prácticas agrícolas sostenibles.
Fórmula:C41H65NO10
InChI:InChI=1S/C41H65NO10/c1-10-26-12-11-13-34(52-36-17-16-33(42(5)6)23(3)48-36)22(2)37(44)32-20-30-28(31(32)21-35(43)50-26)15-14-25-18-27(19-29(25)30)51-41-40(47-9)39(46-8)38(45-7)24(4)49-41/h14-15,20,22-31,33-34,36,38-41H,10-13,16-19,21H2,1-9H3/t22-,23-,24+,25-,26+,27-,28-,29-,30-,31+,33+,34+,36+,38+,39-,40-,41+/m1/s1
Clave InChI:InChIKey=SRJQTHAZUNRMPR-UYQKXTDMSA-N
SMILES:O([C@H]1C[C@]2([C@]3([C@]([C@]4(C(=C3)C(=O)[C@H](C)[C@@H](O[C@@H]5O[C@H](C)[C@@H](N(C)C)CC5)CCC[C@H](CC)OC(=O)C4)[H])(C=C[C@@]2(C1)[H])[H])[H])[H])[C@H]6[C@H](OC)[C@H](OC)[C@@H](OC)[C@H](C)O6
Sinónimos:- (-)-Spinosyn A
- (2R,3aS,5aR,5bS,9S,13S,14R,16aS,16bR)-13-{[(2R,5S,6R)-5-(dimethylamino)-6-methyltetrahydro-2H-pyran-2-yl]oxy}-9-ethyl-14-methyl-7,15-dioxo-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-1H-as-indaceno[3,2-d]oxacyclododecin-2-yl 6-deoxy-2,3,4-tri-O-methyl-alpha-L-mannopyranoside
- (2R,3aS,5aR,5bS,9S,13S,14R,16aS,16bR)-2-[(6-Deoxy-2,3,4-tri-O-methyl-α-<span class="text-smallcaps">L</span>-mannopyranosyl)oxy]-13-[[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,5a,5b,6,9,10,11,12,13,14,16a,16b-tetradecahydro-14-methyl-1H-as-indaceno[3,2-d]oxacyclododecin-7,15-dione
- (2R,3aS,5aR,5bS,9S,14R,16aS,16bR)-13-{[(2R,5S,6R)-5-(dimethylamino)-6-methyltetrahydro-2H-pyran-2-yl]oxy}-9-ethyl-14-methyl-7,15-dioxo-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-1H-as-indaceno[3,2-d]oxacyclododecin-2-yl 6-deoxy-2,3,4-tri-O-methyl-alpha-L-mannopyranoside
- (5aR,5bS,14R,16bR)-13-{[5-(dimethylamino)-6-methyltetrahydro-2H-pyran-2-yl]oxy}-9-ethyl-14-methyl-7,15-dioxo-2,3,3a,5a,5b,6,7,9,10,11,12,13,14,15,16a,16b-hexadecahydro-1H-as-indaceno[3,2-d]oxacyclododecin-2-yl 6-deoxy-2,3,4-tri-O-methylhexopyranoside
- 1H-as-Indaceno[3,2-d]oxacyclododecin-7,15-dione, 2-[(6-deoxy-2,3,4-tri-O-methyl-α-<span class="text-smallcaps">L</span>-mannopyranosyl)oxy]-13-[[(2R,5S,6R)-5-(dimethylamino)tetrahydro-6-methyl-2H-pyran-2-yl]oxy]-9-ethyl-2,3,3a,5a,5b,6,9,10,11,12,13,14,16a,16b-tetradecahydro-14-methyl-, (2R,3aS,5aR,5bS,9S,13S,14R,16aS,16bR)-
- 2-D)Oxacyclododecin-7,15-Dione,2,3,3A,5A,5B,6,9,10,11,12,13,14,16A,16B-Tetradecahydro-2-((6-Deoxy-2,3,4-Tri-O-Methyl-Alpha-L-Mannopyranosyl)Oxy)-13-((5-Dimethylamino)Tetrahydro-6-Methyl-2H-Pyran-2-Yl)
- A 83543A
- Lepicidin A
- Mixture of Spinosyn A and Spinosyn D
- Spinosad A
- spinosyn D
- (2R,3aS,5aR,5bS,9S,13S,14R,16aS,16bR)-2-[(6-Deoxy-2,3,4-tri-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,5a,5b,6,9,10,11,12,13,14,16a,16b-tetradecahydro-14-methyl-1H-as-indaceno[3,2-d]oxacyclododecin-7,15-dione
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Spinosyn A
CAS:Spinosyn A is a polyketide-derived macrolide produced by Saccharopolyspora spinosa and is an active ingredient in several commercial insecticides.Fórmula:C41H65NO10Pureza:99.85%Forma y color:SolidPeso molecular:731.9555Spinosyn A 100 µg/mL in Acetonitrile
CAS:Producto controladoFórmula:C41H65NO10Forma y color:Single SolutionPeso molecular:731.96GB 23200.121-2021 Pesticide Mixture 7 50 µg/mL in Acetonitrile
CAS:Producto controlado- 1014-70-6
- 102851-06-9
- 10369-83-2
- 105843-36-5
- 120067-83-6
- 121552-61-2
- 122-34-9
- 130000-40-7
- 131549-75-2
- 131929-60-7
- 131929-63-0
- 135410-20-7
- 138261-41-3
- 148-79-8
- 150824-47-8
- 165252-70-0
- 1912-24-9
- 21087-64-9
- 210880-92-5
- 21725-46-2
- 33629-47-9
- 40487-42-1
- 41483-43-6
- 53112-28-0
- 5915-41-3
- 7287-19-6
- 75736-33-3
- 834-12-8
- 862588-11-2
- 865318-97-4
- 96525-23-4
Forma y color:MixtureSpinosyn A
CAS:Applications Spinosyn A is a potent insecticide for pathogens of crops and disruptor of nicotinic acetylcholine receptor.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the packageFórmula:C41H65NO10Forma y color:NeatPeso molecular:731.96Spinosad
CAS:Fórmula:C41H65NO10(A)C42H67NO10(D)Pureza:≤ 5.0%Forma y color:White or almost white crystalline powderPeso molecular:731.95 (A); 745.98 (D)Spinosad A (Spinosyn A) in Acetonitrile
CAS:AcetonitrileFórmula:C41H65NO10Forma y color:White odorless solid; [Merck Index]Peso molecular:732.0Spinosyn A
CAS:Fórmula:C41H65NO10Forma y color:White odorless solid; [Merck Index]Peso molecular:732.0Spinosad A(Spinosyn A) in Acetonitrile
CAS:AcetonitrileFórmula:C41H65NO10Forma y color:White odorless solid; [Merck Index]Peso molecular:732.0Spinosad A (Spinosyn A)
CAS:Fórmula:C41H65NO10Forma y color:White odorless solid; [Merck Index]Peso molecular:732.0(2R,3aS,5aR,5bS,9S,13S,14R,16aS,16bR)-2-[(6-Deoxy-2,3,4-tri-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,5a,5b,6,9,10,11,12,13,14,16a,16b-tetradecahydro-14-methyl-1H-as-indaceno[3,2-d]oxacyclododecin-7,15-dione
CAS:Fórmula:C41H65NO10Pureza:90%Forma y color:SolidPeso molecular:731.9555Spinosyn A
CAS:Spinosyn A is a natural insecticide, which is derived from the fermentation of the soil bacterium *Saccharopolyspora spinosa*. It exhibits a unique mode of action as it targets the nicotinic acetylcholine receptors of the insect nervous system. This interaction results in hyperexcitation of the insect neurons, leading to paralysis and ultimately death.Fórmula:C41H65NO10Pureza:Min. 95%Peso molecular:731.96 g/molRef: 3D-FS170614
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