Date published: 2026-5-8

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Tritriacontane (CAS 630-05-7)

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CAS Number:
630-05-7
Molecular Weight:
464.89
Molecular Formula:
C33H68
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Tritriacontane is a long-chain hydrocarbon that functions as a nonpolar solvent in experiment. It interacts with other nonpolar compounds, such as lipids and waxes, by forming weak dispersion forces. This allows Tritriacontane to dissolve nonpolar substances and facilitate their manipulation in laboratory experiments. At the molecular level, Tritriacontane′s long hydrocarbon chain enables it to interact with other nonpolar molecules through van der Waals forces, aiding in the separation and analysis of nonpolar compounds. Its mechanism of action involves creating a nonpolar environment, which is useful for studying the behavior of nonpolar substances in various experiment. Tritriacontane′s nonpolar nature allows it to act as a protective coating for sensitive materials, preventing unwanted interactions with polar substances during experimental procedures.


Tritriacontane (CAS 630-05-7) References

  1. Organ-dependent modifying effects of caffeine, and two naturally occurring antioxidants alpha-tocopherol and n-tritriacontane-16,18-dione, on 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP)-induced mammary and colonic carcinogenesis in female F344 rats.  |  Hagiwara, A., et al. 1999. Jpn J Cancer Res. 90: 399-405. PMID: 10363577
  2. Characterization of waxes used in pictorial artworks according to their relative amount of fatty acids and hydrocarbons by gas chromatography.  |  Peris-Vicente, J., et al. 2006. J Chromatogr A. 1101: 254-60. PMID: 16246351
  3. Modifying effects of the naturally occurring antioxidants gamma-oryzanol, phytic acid, tannic acid and n-tritriacontane-16, 18-dione in a rat wide-spectrum organ carcinogenesis model.  |  Hirose, M., et al. 1991. Carcinogenesis. 12: 1917-21. PMID: 1657429
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  7. Visualization of Crystallographic Orientation and Twist Angles in Two-Dimensional Crystals with an Optical Microscope.  |  Cui, X., et al. 2020. Nano Lett. 20: 6059-6066. PMID: 32584585
  8. Cuticular hydrocarbons as a tool for determining the age of Chrysomya rufifacies (Diptera: Calliphoridae) larvae.  |  Sharma, A., et al. 2021. J Forensic Sci. 66: 236-244. PMID: 32966626
  9. Sub-lethal effects of the consumption of Eupatorium buniifolium essential oil in honeybees.  |  Rossini, C., et al. 2020. PLoS One. 15: e0241666. PMID: 33147299
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  11. Inhibitory effects of 1-O-hexyl-2,3,5-trimethylhydroquinone (HTHQ), green tea catechins and other antioxidants on 2-amino-6-methyldipyrido[1,2-a:3',2'-d]imidazole (Glu-P-1)-induced rat hepatocarcinogenesis and dose-dependent inhibition by HTHQ of lesion induction by Glu-P-1 or 2-amino-3,8-dimethylimidazo[4,5-f]quinoxaline (MeIQx).  |  Hirose, M., et al. 1995. Carcinogenesis. 16: 3049-55. PMID: 8603484
  12. Structure of the ascarosides from Ascaris suum.  |  Bartley, JP., et al. 1996. J Nat Prod. 59: 921-6. PMID: 8904841
  13. Effects of n-tritriacontane-16,18-dione, curcumin, chlorphyllin, dihydroguaiaretic acid, tannic acid and phytic acid on the initiation stage in a rat multi-organ carcinogenesis model.  |  Takaba, K., et al. 1997. Cancer Lett. 113: 39-46. PMID: 9065799

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Tritriacontane, 250 mg

sc-251406
250 mg
$94.00