h
hexacosane
Chemical compound
Also known as CH3-[CH2]24-CH3 · n-hexacosane
- Formula
- C₂₆H₅₄
1
- C₂₆H₅₄
- Mass
- 366.423 Da
1
- 366.423 Da
- Melting point
- 57°C
1
- 57°C
- Boiling point
- 685.35 K
Chemistry
All data
111 statements · 82% with external sources · numbers in brackets are citations
- Canonical SMILES
- CCCCCCCCCCCCCCCCCCCCCCCCCC
1
- CCCCCCCCCCCCCCCCCCCCCCCCCC
- Found in taxon
- Euphorbia watanabei
1
- Plantago asiatica
1
- Plantago major
1
- Convolvulus arvensis
- Agave decipiens
- Arctostaphylos patula
- Hypericum perforatum
- Hypericum maculatum
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- Hypericum olympicum
- Daphne odora
- Diplotaxis harra
- Erucaria microcarpa
- Sesbania grandiflora
- Spathiphyllum cannifolium
- Proiphys amboinensis
- Vitex agnus-castus
- Vanilla planifolia
- Vanilla madagascariensis
- Vanilla tahitensis
- Hamamelis virginiana
- Nelumbo lutea
1
- Rosa × centifolia
- Plantago ovata
- Zinnia elegans
- Cistus ladanifer
- Cistus laurifolius
- Cistus monspeliensis
- Scutellaria baicalensis
1
- Nepeta hindostana
1
- Clusia spiritu-sanctensis
- Mandragora autumnalis
1
- Mandragora officinarum
1
- Anagallis arvensis
1
- Ligularia veitchiana
- Sideritis taurica
- Tamarindus indica
- Cynomorium songaricum
- Abutilon indicum
1
- Alstonia scholaris
- Annona squamosa
- Arnica montana
- Casearia ilicifolia
1
- Cestrum nocturnum
- Cryptotermes brevis
- Dactylanthus taylorii
- Digitalis purpurea
1
- Diospyros malabarica
1
- Echinacea angustifolia
- Euphorbia lactiflua
- Sidera lenis
- cherry laurel
- Verbascum lasianthum
- Formosan subterranean termite
- Zootermopsis angusticollis
- Cannabis sativa
- Salvia triloba
1
- potato
- Artemisia annua
- Murraya paniculata
- Ruta graveolens
2
Sources- 1.Stated in High-resolution gas-chromatographic analysis of the secondary metabolites obtained by subcritical-fluid extraction from Colombian rue (Ruta graveolens L.).
- 2.Stated in Concentration of Ruta graveolens active compounds using SC-CO 2 extraction coupled with fractional separation
- Euphorbia watanabei
On other databases
26 identifiers linking hexacosane across the web's reference databases
- CAMEO Chemicals ID20468
- Cannabis Database ID000163
- CAS Registry Number630-01-3
- ChEBI ID32940
- ChemSpider ID11901
- DSSTOX compound identifierDTXCID3043601
- DSSTox substance IDDTXSID7060883
- EC number211-124-1
- ECHA Substance Infocard ID100.010.114
- Google Knowledge Graph ID/g/1213v2kc
- HSDB ID8356
- Human Metabolome Database IDHMDB0061867
- InChIInChI=1S/C26H54/c1-3-5-7-9-11-13-15-17-19-21-23-25-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-26H2,1-2H3
- InChIKeyHMSWAIKSFDFLKN-UHFFFAOYSA-N
- J-GLOBAL ID200907069627771894
- KNApSAcK IDC00030478
- LIPID MAPS IDLMFA11000576
- MassBank accession IDMSBNK-Fac_Eng_Univ_Tokyo-JP009123
- Nikkaji IDJ527D
- NSC number122457
- PubChem CID12407
- Reaxys registry number1705609
- SPLASHsplash10-0a4l-9000000000-e37e2b4f024d8a92f5a7
- SureChEMBL ID198427
- UniChem compound ID1097639
- UNII0CI4OKE9VO