| Identification | Back Directory | [Name]
KINOPRENE | [CAS]
42588-37-4 | [Synonyms]
ZR 77
xr777
enstar
Altodel
ent70531
ENSTAR(R)
KINOPRENE
enstarigr
KINOPRENE, 100MG, NEAT
FZRBKIRIBLNOAM-WHVZTFIZSA-N
kinoprene (bsi, e-iso, f-iso)
(e,e)-2-propynyl3,7,11-trimethyl-2,4-dodecadienoate
2-PROPYNYL-(E,E)-3,7,11-TRIMETHYL-2,4-DODECADIENOATE
(e,e)-3,7,11-trimethyl-2,4-dodecadienoicacid2-propynylester
3,7,11-trimethyl-,2-propynylester,(e,e)-4-dodecadienoicacid
(2E,4E)-3,7,11-Trimethyldodeca-2,4-dienoic acid 2-propynyl ester
(2E,4E)-3,7,11-Trimethyl-2,4-dodecadienoic acid 2-propyn-1-yl ester
2,4-Dodecadienoic acid, 3,7,11-trimethyl-, 2-propyn-1-yl ester, (2E,4E)- | [EINECS(EC#)]
255-898-9 | [Molecular Formula]
C18H28O2 | [MDL Number]
MFCD01310427 | [MOL File]
42588-37-4.mol | [Molecular Weight]
276.41 |
| Chemical Properties | Back Directory | [Melting point ]
<25℃ | [Boiling point ]
bp0.04 115-116° | [density ]
1.0356 (rough estimate) | [refractive index ]
1.4800 (estimate) | [Fp ]
40.5 °C | [solubility ]
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) | [form ]
Oil | [color ]
Colourless | [Henry's Law Constant]
1.8×10-1 mol/(m3Pa) at 25℃, Ebert et al. (2023) | [Stability:]
Light Sensitive | [EPA Substance Registry System]
Kinoprene (42588-37-4) |
| Safety Data | Back Directory | [Risk Statements ]
10 | [RIDADR ]
UN1993 3/PG 3 | [RTECS ]
JR1730000 | [HS Code ]
29161900 | [Toxicity]
LD50 oral in rat: 4900mg/kg |
| Hazard Information | Back Directory | [Uses]
Insect growth regulator. | [Definition]
ChEBI: Kinoprene is a farnesane sesquiterpenoid and a terminal acetylenic compound. It has a role as a juvenile hormone mimic. | [Production Methods]
Kinoprene is synthetically produced through a multi-step chemical process designed to yield the active juvenile hormone analog. The synthesis typically begins with the preparation of a dodecadienoate backbone, incorporating two conjugated double bonds at specific positions to mimic the natural juvenile hormone structure. Key intermediates include alkyl-substituted dienes and esterification agents, which are reacted under controlled conditions, often involving acid catalysis and temperature regulation, to form the final compound. | [Mechanism of action]
Inhibits normal insect growth during the moulting process. Juvenile hormone mimic. | [Pesticide Type]
Insecticide |
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