Limonene

Assemble a molecular structure model of Limonene using Genuine Molymod Components by indigoinstruments.com

D-limonene's insecticidal mechanism is attributed to its disrupting cell membranes and respiratory structures of insects. Limonene penetrates insect cuticles to attack cell membranes which leads to dehydration & loss of essential ions. It is also believed to interfere with insect respiratory enzymes affecting gas exchange of oxygen and carbon dioxide. It may also be neurotoxic & disrupts neurotransmitter communication between nerve cells causing paralysis and death. Limonene may have use as a natural pesticide on ornamental plants with thick, waxy leaves, such as palms, cycads, and orchids.

A molecular model of Limonene in the Molymod Hybrid Dome style uses the atoms & bonds in the parts list below. Our free 3D Molecular Model Builder shows other styles & allows for image rotation as an assembly guide.

Chemical data
Molecular Weight Chemical Formula
136.2364 C10H16
Parts
P/NDescriptionQTY
60150EAtom, Molymod, white (hydrogen), hemisphere, 19mm16
60400EAtom, Molymod, black (carbon), 4 hole, 109.5 degrees, 23mm10
61012EBond, Molymod, grey (single), 20mm8
61013EBond, Molymod, grey (double/triple), 35mm4
61015EBond, Molymod, opaque, 2mm (for spacefilling models)16
Synonyms
  • IUPAC Name: (4R)-1-methyl-4-prop-1-en-2-ylcyclohexene
  • InChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,10H,1,5-7H2,2-3H3/t10-/m0/s1
  • InChIKey: XMGQYMWWDOXHJM-JTQLQIEISA-N
  • SMILES: CC1=CCC(CC1)C(=C)C
  • CAS: 5989-27-5
  • d-Limonene
  • Cajeputene
  • Dipentene
  • Kautschin
  • Cajeputen
  • Cinen
  • Cinene
  • Dipenten
  • Eulimen
  • Nesol
  • Dipanol
  • Flavor orange
  • Terpodiene
  • beta-Limonene
  • Carvene
  • Citrene