Spinosad structure, CAS 131929-60-7

Spinosad

CAS Number131929-60-7

SynonymsRAMOPLANIN; SPINOSYN A; Spinosad; Spinosyn D

Molecular FormulaC41H65NO10

Molecular Weight731.956

Purity98.00%

Density1.2±0.1 g/cm3

Boiling Point801.5±65.0 °C at 760 mmHg

Melting Point84ºC to 99.5ºC

Flash Point

Appearance

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Cat. No.: 2A-9052157 Purity: 98.00%
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Quality Control of [ 131929-60-7 ] Purity: 98.00% SDS Specification MoL

Chemical & Physical Properties
CAS Number131929-60-7
Catalog No.2A-9052157
Chinese Name多杀菌素
SynonymsRAMOPLANIN; SPINOSYN A; Spinosad; Spinosyn D
Molecular FormulaC41H65NO10
Molecular Weight731.956
Purity98.00
Density1.2±0.1 g/cm3
Boiling Point801.5±65.0 °C at 760 mmHg
Melting Point84ºC to 99.5ºC
PackagingIII
ApplicationSpinosyn A is a polyketide-derived macrolide produced by Saccharopolyspora spinosa and is an effective insecticide [1].
HTC2932209090
SMILESCCC1CCCC(OC2CCC(N(C)C)C(C)O2)C(C)C(=O)C2=CC3C(C=CC4CC(OC5OC(C)C(OC)C(OC)C5OC)CC43)C2CC(=O)O1
InChIInChI=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
InChI KeySRJQTHAZUNRMPR-UYQKXTDMSA-N
MSDSmsds/52157_1_131929_60_7.pdf
Use ofSpinosyn A, a polyketide-derived macrolide produced by Saccharopolyspora spinosa, is a potent insecticide[1]. Properties Name spinosyn A Synonym More Synonyms Spinosad Biological Activity Description Spinosyn A, a polyketide-derived macrolide produced by Saccharopolyspora spinosa, is a potent insecticide[1]. Related Catalog Research Areas >> Others Signaling Pathways >> Others >> Others In Vitro Spinosad is a mixture of two natural occurring macrocyclic lactones (spinosyn A and spinosyn D) and acts primarily as a nAChR agonist[2]. References [1]. Hak Joong Kim, et al. Biosynthesis of spinosyn in Saccharopolyspora spinosa: synthesis of permethylated rhamnose and characterization of the functions of SpnH, SpnI, and SpnK. J Am Chem Soc. 2010 Mar 10;132(9):2901-3. [2]. D T Vo, et al. Insect nicotinic acetylcholine receptor agonists as flea adulticides in small animals. J Vet Pharmacol Ther. 2010 Aug;33(4):315-22. Chemical & Physical Properties Molecular Formula C41H65NO10 Exact Mass 731.460876 PSA 111.22000 Index of Refraction 1.540 InChIKey SRJQTHAZUNRMPR-UYQKXTDMSA-N Safety Information RIDADR UN 3077 Packaging Group III HS Code 2932209090 Synthetic Route 5-Oxo-pentanoic... 131929-60-7 Literature: Paquette, Leo A.; Collado, Ivan; Purdie, Mark Journal of the American Chemical Society, 1998 , vol. 120, # 11 p. 2553 - 2562 56587-30-5 131929-60-7 Literature: Paquette, Leo A.; Collado, Ivan; Purdie, Mark Journal of the American Chemical Society, 1998 , vol. 120, # 11 p. 2553 - 2562 118545-01-0 131929-60-7 Literature: Paquette, Leo A.; Collado, Ivan; Purdie, Mark Journal of the American Chemical Society, 1998 , vol. 120, # 11 p. 2553 - 2562
Tax Rebate13.0%
SupervisionNone. MFN tariff: 6.5%. Ordinary tariff: 20.0%
Transport InfoProduct name: Summary 2932209090. other lactones. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
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