2-Undecanone

For research use only. Not for therapeutic Use.

  • CAT Number: R042772
  • CAS Number: 112-12-9
  • Molecular Formula: C11H22O
  • Molecular Weight: 170.296
  • Purity: ≥95%
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<span style="color:#000000;"><span style="font-family:arial,helvetica,sans-serif;"><span style="font-size:12px;">2-Undecanone (CAS&nbsp;112-12-9)&nbsp;<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">occurs naturally in wild tomato.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;It is also found in&nbsp;</span><i style="color: rgb(102, 94, 88); font-family: Arial, Helvetica, sans-serif; font-variant-ligatures: normal; orphans: 2; widows: 2;">Ruta chalepensis</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;essential oil and hop oil.&nbsp;</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">2-Undecanone is an insect and tick repellant.</span></span></span></span>


Catalog Number R042772
CAS Number 112-12-9
Synonyms

2-Hendecanone; BioUD; BioUD 30; BioUD 8; Methyl n-Nonyl Ketone; Methyl Nonyl Ketone; Mostique EGX 101; NSC 4028; Nonyl Methyl Ketone

Molecular Formula C11H22O
Purity ≥95%
Target Disease Research Fields
Storage -20°C
IUPAC Name undecan-2-one
InChI InChI=1S/C11H22O/c1-3-4-5-6-7-8-9-10-11(2)12/h3-10H2,1-2H3
InChIKey KYWIYKKSMDLRDC-UHFFFAOYSA-N
SMILES CCCCCCCCCC(=O)C
Reference

<span style="color:#000000;"><span style="font-size:12px;"><span style="font-family:arial,helvetica,sans-serif;">1.<span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Farrar Jr, Robert R., and George G. Kennedy. &quot;2‐Undecanone, a constituent of the glandular trichomes of Lycopersicon hirsutum f. glabratum: effects on Heliothis zea and Manduca sexta growth and survival.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Entomologia experimentalis et Applicata</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;43.1 (1987): 17-23.<br />
2.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Baser, K. H. C., Temel &Ouml;zek, and S. H. Beis. &quot;Constituents of the essential oil of Ruta chalepensis L. from Turkey.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Journal of Essential Oil Research</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;8.4 (1996): 413-414.<br />
3.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Witting-Bissinger, B. E., et al. &quot;Novel arthropod repellent, BioUD, is an efficacious alternative to deet.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Journal of medical entomology</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;45.5 (2008): 891-898.<br />
4.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Bohbot, J. D., et al. &quot;Multiple activities of insect repellents on odorant receptors in mosquitoes.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Medical and veterinary entomology</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;25.4 (2011): 436-444.<br />
5.</span><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">Whang, Hyun Suk, and Alan Tonelli. &quot;Release characteristics of the non-toxic insect repellant 2-undecanone from its crystalline inclusion compound with &alpha;-cyclodextrin.&quot;&nbsp;</span><i style="font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;">Journal of Inclusion Phenomena and Macrocyclic Chemistry</i><span style="font-variant-ligatures: normal; orphans: 2; widows: 2;">&nbsp;62.1-2 (2008): 127-134.</span></span></span></span>

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