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Abamectin

PESTANAL®, analytical standard

Synonym(s):

Avermectin B1

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About This Item

CAS Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

storage temp.

−20°C

SMILES string

CCC(C)C1O[C@@]2(C[C@@H]3CC(C\C=C(C)\[C@@H](O[C@H]4C[C@H](OC)[C@@H](O[C@H]5C[C@H](OC)[C@@H](O)[C@H](C)O5)[C@H](C)O4)[C@@H](C)\C=C\C=C6/COC7[C@H](O)C(C)=CC(C(=O)O3)[C@]67O)O2)C=C[C@@H]1C

InChI

1S/C48H72O14/c1-11-25(2)43-28(5)17-18-47(62-43)23-34-20-33(61-47)16-15-27(4)42(26(3)13-12-14-32-24-55-45-40(49)29(6)19-35(46(51)58-34)48(32,45)52)59-39-22-37(54-10)44(31(8)57-39)60-38-21-36(53-9)41(50)30(7)56-38/h12-15,17-19,25-26,28,30-31,33-45,49-50,52H,11,16,20-24H2,1-10H3/b13-12+,27-15+,32-14+/t25-,26-,28-,30-,31-,33+,34-,35?,36-,37-,38-,39-,40+,41-,42-,43+,44-,45+,47+,48+/m0/s1

InChI key

RRZXIRBKKLTSOM-RDKIRRGNSA-N

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General description

Abamectin (MK-0936) belongs to avermectin family. This family have a macrocycle as backbone with a spiroketal unit, a hexahydrobenzofuran unit and disaccharide substitute in general. MK-0936 is a natural fermenting product which can be produced by Streptomyces avermitilis.

Application

Abamectin has been used as standard in liquid chromatography–electrospray tandem mass spectrometry LC–ESI-MS–MS method for determination of abamectin residues in orange samples.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Classifications

Acute Tox. 1 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 2 - STOT RE 1

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Determination of abamectin and azadirachtin residues in orange samples by liquid chromatography?electrospray tandem mass spectrometry.
Pozo, O. J., et al.
Journal of Chromatography A, 992.1, 133-140 (2003)
Xiaojie Liu et al.
Frontiers in plant science, 8, 903-903 (2017-06-15)
The high structural diversity of plant metabolites suggests that interactions among them should be common. We investigated the effects of single metabolites and combinations of plant metabolites on insect herbivores. In particular we studied the interacting effects of pyrrolizidine alkaloid
Kang Qiao et al.
Pest management science, 68(6), 853-857 (2012-03-08)
Tomato growers in Shandong Province, China, commonly face heavy root-knot nematode infestations. Current methods of control include cadusafos and methyl bromide (MeBr), but alternative methods are required because of the high toxicity of these pesticides and the ecological risk of
Andréa Novelli et al.
Ecotoxicology and environmental safety, 75(1), 87-93 (2011-09-23)
The present study aimed to evaluate the interactions of the pesticide Vertimec(®) 18EC in aquatic ecosystems. In this respect, soil plots were contaminated with Vertimec(®) 18EC at the concentration indicated for strawberry crops (0.125L of solution m(-2)). After the contamination
W Dermauw et al.
Insect biochemistry and molecular biology, 42(7), 455-465 (2012-04-03)
The cys-loop ligand-gated ion channel (cysLGIC) super family of Tetranychus urticae, the two-spotted spider mite, represents the largest arthropod cysLGIC super family described to date and the first characterised one within the group of chelicerates. Genome annotation, phylogenetic analysis and

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