Date published: 2025-10-21

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4-Heptanol (CAS 589-55-9)

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Alternate Names:
Dipropylcarbinol
CAS Number:
589-55-9
Molecular Weight:
116.20
Molecular Formula:
C7H16O
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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4-Heptanol is an organic alcohol that finds utility in various research applications primarily within organic synthesis and material science. As a medium-chain alcohol, it is often used as a solvent or a reagent in the synthesis of more complex organic molecules, where its hydrophobic alkyl chain and hydrophilic hydroxyl group enable it to interact with a wide range of chemical species. The compound′s ability to undergo oxidation reactions makes it a candidate for studying the mechanisms of alcohol oxidation and for use in creating derivatives with different functional groups. In the realm of materials science, 4-heptanol is investigated for its potential as a plasticizer in polymer formulations, which can affect the flexibility and durability of plastic materials. Additionally, its surface-active properties are explored in the formation and stabilization of emulsions, which is relevant to the production of coatings, adhesives, and food technology.


4-Heptanol (CAS 589-55-9) References

  1. Solvent effect on ion-pair extraction of 2-(2-pyridylazo)-1-naphthol-4-sulfonate anion with solvated hydroxonium ion using alcohols and 1-octanol/octane mixed solvents.  |  Naito, T., et al. 2001. Anal Sci. 17: 291-5. PMID: 11990543
  2. Exocrine chemistry of the myrmicine ant Zacryptocerus pusillus (Hymenoptera: Formicidae).  |  Morgan, ED., et al. 2006. Arch Insect Biochem Physiol. 63: 11-4. PMID: 16921517
  3. Preparation of polypyrrole composite solid-phase microextraction fiber coatings by sol-gel technique for the trace analysis of polar biological volatile organic compounds.  |  Zhang, Z., et al. 2013. Analyst. 138: 1156-66. PMID: 23282483
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  5. RIFM fragrance ingredient safety assessment, 4-heptanol, 2,6-dimethyl-,acetate, CAS Registry Number 10250-45-0.  |  Api, AM., et al. 2019. Food Chem Toxicol. 134 Suppl 1: 110603. PMID: 31238148
  6. Purification and properties of a polyvinyl alcohol-degrading enzyme produced by a strain of Pseudomonas.  |  Watanabe, Y., et al. 1976. Arch Biochem Biophys. 174: 575-81. PMID: 820265
  7. Oxidation of Secondary Alcohols by Polyvinyl Alcohol-degrading Enzyme Produced by Pseudomonas O–3  |  Suzuki, T. 1978. Agricultural and Biological Chemistry. 42(6): 1187-1194.
  8. Purification and properties of secondary alcohol oxidase from a strain of Pseudomonas  |  Morita, M., Hamada, N., Sakai, K., & Watanabe, Y. 1979. Agricultural and Biological Chemistry. 43(6): 1225-1235.
  9. Solubilization of heptanols and α, ω-alkanediols in aqueous solutions of sodium dodecyl sulfate  |  Blokhus, A. M., Høiland, H., & Backlund, S. 1986. Journal of colloid and interface science. 114(1): 9-15.
  10. Liquid-crystalline solvents as mechanistic probes. Part 37. Novel family of gelators of organic fluids and the structure of their gels  |  Lin, Y. C., Kachar, B., & Weiss, R. G. 1989. Journal of the American Chemical Society. 111(15): 5542-5551.
  11. Mesoporous MgO and Ni–MgO prepared by using carboxylic acids  |  Takenaka, S., Sato, S., Takahashi, R., & Sodesawa, T. 2003. Physical Chemistry Chemical Physics. 5(21): 4968-4973.
  12. A novel secondary alcohol dehydrogenase from Micrococcus luteus WIUJH20: purification, cloning, and properties  |  Huang, J. K., Park, J. K., Dhungana, B. R., Youngblut, N. D., Lin, C. T., & Wen, L. 2010. The FASEB Journal. 24: 835-5.
  13. Volatile components from the mandibular glands of the turtle ants, Cephalotes alfaroi and Cephalotes cristatus  |  Wood, W. F., Hoang, T. T., & McGlynn, T. P. 2011. Biochemical Systematics and Ecology. 39(2): 135-138.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Heptanol, 25 ml

sc-487173
25 ml
$97.00