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Nonacosane

Nonacosane is a straight-chain hydrocarbon with a molecular formula of C29H60, and the structural formula CH3(CH2)27CH3. It has 1,590,507,121 constitutional isomers.

Nonacosane
Names
Preferred IUPAC name
Nonacosane[1]
Identifiers
  • 630-03-5 Y
3D model (JSmol)
  • Interactive image
1724922
ChEBI
  • CHEBI:7613 N
ChEMBL
  • ChEMBL428955 Y
ChemSpider
  • 11903 Y
ECHA InfoCard 100.010.116
EC Number
  • 211-126-2
KEGG
  • C08384 Y
MeSH nonacosane
  • 12409
UNII
  • IGL1697BK1 Y
  • DTXSID2060884
  • InChI=1S/C29H60/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-29H2,1-2H3 Y
    Key: IGGUPRCHHJZPBS-UHFFFAOYSA-N Y
  • CCCCCCCCCCCCCCCCCCCCCCCCCCCCC
Properties
C29H60
Molar mass 408.799 g·mol−1
Appearance White, opaque, waxy crystals
Odor Odorless
Density 0.8083 g cm−3
Melting point 62 to 66 °C; 143 to 151 °F; 335 to 339 K
Boiling point 440.9 °C; 825.5 °F; 714.0 K
log P 15.482
Related compounds
Related alkanes
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)

Nonacosane occurs naturally and has been reported to be a component of a pheromone of Orgyia leucostigma,[2] and evidence suggests it plays a role in the chemical communication of several insects, including the female Anopheles stephensi (a mosquito).[3]

Nonacosane has been identified within several essential oils. It can also be prepared synthetically.[4]

References edit

  1. ^ "nonacosane - Compound Summary". PubChem Compound. USA: National Center for Biotechnology Information. 16 September 2004. Identification and Related Records. Retrieved 2 January 2012.
  2. ^ Pheromone identification
  3. ^ Brei B, Edman JD, Gerade B, Clark JM (2004). "Relative abundance of two cuticular hydrocarbons indicates whether a mosquito is old enough to transmit malaria parasites". J. Med. Entomol. 41 (4): 807–9. doi:10.1603/0022-2585-41.4.807. PMID 15311480.
  4. ^ Bentley, H.R.; Henry, J.A.; Irvine, D.S.; Mukerji, D. & Spring, F.S. (1955). "Triterpenoids. Part XXXII. cyclolaudenol, a triterpenoid alcohol from opium". J. Chem. Soc.: 596–602. doi:10.1039/jr9550000596.

nonacosane, straight, chain, hydrocarbon, with, molecular, formula, c29h60, structural, formula, 27ch3, constitutional, isomers, namespreferred, iupac, name, identifierscas, number, model, jsmol, interactive, imagebeilstein, reference, 1724922chebi, chebi, 761. Nonacosane is a straight chain hydrocarbon with a molecular formula of C29H60 and the structural formula CH3 CH2 27CH3 It has 1 590 507 121 constitutional isomers Nonacosane NamesPreferred IUPAC name Nonacosane 1 IdentifiersCAS Number 630 03 5 Y3D model JSmol Interactive imageBeilstein Reference 1724922ChEBI CHEBI 7613 NChEMBL ChEMBL428955 YChemSpider 11903 YECHA InfoCard 100 010 116EC Number 211 126 2KEGG C08384 YMeSH nonacosanePubChem CID 12409UNII IGL1697BK1 YCompTox Dashboard EPA DTXSID2060884InChI InChI 1S C29H60 c1 3 5 7 9 11 13 15 17 19 21 23 25 27 29 28 26 24 22 20 18 16 14 12 10 8 6 4 2 h3 29H2 1 2H3 YKey IGGUPRCHHJZPBS UHFFFAOYSA N YSMILES CCCCCCCCCCCCCCCCCCCCCCCCCCCCCPropertiesChemical formula C 29H 60Molar mass 408 799 g mol 1Appearance White opaque waxy crystalsOdor OdorlessDensity 0 8083 g cm 3Melting point 62 to 66 C 143 to 151 F 335 to 339 KBoiling point 440 9 C 825 5 F 714 0 Klog P 15 482Related compoundsRelated alkanes TetracosaneHentriacontaneExcept where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa N verify what is Y N Infobox references Nonacosane occurs naturally and has been reported to be a component of a pheromone of Orgyia leucostigma 2 and evidence suggests it plays a role in the chemical communication of several insects including the female Anopheles stephensi a mosquito 3 Nonacosane has been identified within several essential oils It can also be prepared synthetically 4 References edit nonacosane Compound Summary PubChem Compound USA National Center for Biotechnology Information 16 September 2004 Identification and Related Records Retrieved 2 January 2012 Pheromone identification Brei B Edman JD Gerade B Clark JM 2004 Relative abundance of two cuticular hydrocarbons indicates whether a mosquito is old enough to transmit malaria parasites J Med Entomol 41 4 807 9 doi 10 1603 0022 2585 41 4 807 PMID 15311480 Bentley H R Henry J A Irvine D S Mukerji D amp Spring F S 1955 Triterpenoids Part XXXII cyclolaudenol a triterpenoid alcohol from opium J Chem Soc 596 602 doi 10 1039 jr9550000596 Retrieved from https en wikipedia org w index php title Nonacosane amp oldid 1136176477, wikipedia, wiki, book, books, library,

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