All Photos(1)
Synonym(s):
n-Triacontane
Linear Formula:
CH3(CH2)28CH3
CAS Number:
Molecular Weight:
422.81
Beilstein:
1777281
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
bp
258-259 °C/3 mmHg (lit.)
mp
64-67 °C (lit.)
SMILES string
CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
InChI
1S/C30H62/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-30H2,1-2H3
InChI key
JXTPJDDICSTXJX-UHFFFAOYSA-N
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General description
Triacontane is a straight-chain alkane that can be produced from palmitic acid via Kolbe electrolysis.
Interfacial molecular ordering of triacontane, at the SiO2/air interface, for submonolayer and excess coverage has been investigated.
Interfacial molecular ordering of triacontane, at the SiO2/air interface, for submonolayer and excess coverage has been investigated.
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Long chain n-alkanes at SiO2/air interfaces: Molecular ordering, annealing, and surface freezing of triacontane in the case of excess and submonolayer coverage.
Schollmeyer H, et al.
Langmuir, 19(12), 5042-5051 (2003)
Electrochemical conversion of palmitic acid via Kolbe electrolysis for synthesis of n-triacontane
Zhang Y, et al.
Journal of Electroanalytical Chemistry, 822, 73-80 (2018)
Scott A Harding et al.
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Electron microscopy techniques such as transmission electron microscopy (TEM) and scanning electron microscopy (SEM) have been invaluable tools for the study of the micromorphology of plant cuticles. However, for electron microscopy, the preparation techniques required may invariably introduce artefacts in
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Smyrnium olusatrum (Apiaceae), well known as wild celery, is a biennal celery-scented plant used for many centuries as a vegetable, then abandoned after the introduction of celery. In the present work, the essential oil obtained from inflorescences and the amounts
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