C48H72O14
873.1 g/mol
AgrochemicalDanger
8,9-Z-Abamectin B1a
CAS113665-89-7
Category
Agrochemical
Compound Class
Natural Product
Primary Use
Antiparasitic agent for agriculture
8,9-Z-Abamectin B1a is a stereoisomer of abamectin, a macrocyclic lactone compound used as an antiparasitic agent in agriculture. It is a high-molecular-weight, non-aromatic, polyether-rich molecule with multiple rings and hydroxyl groups, reflecting its complex structure.
antiparasitic agent for agricultural use
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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Related Compounds
StrongStructure SimilarSimilarity 0.92
Avermectin A1a
CAS65195-51-9
pharmaceutical raw material
StrongStructure SimilarSimilarity 0.91
Abamectin b1b
CAS65195-56-4
active ingredient in ant bait traps
StrongStructure SimilarSimilarity 0.88
Emamectin
CAS119791-41-2
insecticide
StrongStructure SimilarSimilarity 0.88
Emamectin B1A
CAS121124-29-6
insecticide chloride channel activator
ReferenceSame Category
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CAS114-26-1
nonfood carbamate insecticide
ReferenceSame Category
Glyphosate-monoammonium
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herbicide active ingredient
ReferenceSame Category
Clodinafop
CAS114420-56-3
Phenoxy herbicide
ReferenceSame Category
2,3,6-Trichloro-5-cyano-4-hydroxybenzene-1-carboximidic acid
CAS115044-73-0
pesticide metabolite or intermediate
Related Reading
Safety Reference
Danger
H300Fatal if swallowed
H400Very toxic to aquatic life
H410Very toxic to aquatic life with long lasting effects
Identifiers
IUPAC Name
(1'R,2R,3S,4'S,6S,8'R,10'E,12'S,13'S,14'E,16'Z,20'R,21'R,24'S)-2-[(2S)-butan-2-yl]-21',24'-dihydroxy-12'-[(2R,4S,5S,6S)-5-[(2S,4S,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-3,11',13',22'-tetramethylspiro[2,3-dihydropyran-6,6'-3,7,19-trioxatetracyclo[15.6.1.14,8.020,24]pentacosa-10,14,16,22-tetraene]-2'-one
InChIKey
RRZXIRBKKLTSOM-WEWDGTPISA-N
SMILES
CC[C@H](C)[C@@H]1[C@H](C=C[C@@]2(O1)C[C@@H]3C[C@H](O2)C/C=C(/[C@H]([C@H](/C=C/C=C\4/CO[C@H]5[C@@]4([C@@H](C=C([C@H]5O)C)C(=O)O3)O)C)O[C@H]6C[C@@H]([C@H]([C@@H](O6)C)O[C@H]7C[C@@H]([C@H]([C@@H](O7)C)O)OC)OC)\C)C
Synonyms (2)
- 8,9-Z-Abamectin B1a
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