Date published: 2026-2-7

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6-Heptyn-1-ol (CAS 63478-76-2)

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CAS Number:
63478-76-2
Molecular Weight:
112.17
Molecular Formula:
C7H12O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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6-Heptyn-1-ol is a monohydric alcohol characterized by its colorless liquid state and slightly sweet scent. It has a broad spectrum of uses, ranging from its role in cosmetics to its application in industrial chemicals. Its versatility extends to scientific research, where it′s utilized as a reagent in organic synthesis and as a foundational material for the synthesis of other compounds. It also serves as a solvent for the preparation of organic compounds. Moreover, 6-Heptyn-1-ol is employed in the creation of cosmetics, such as perfumes and fragrances. As a monohydric alcohol, its single hydroxyl group, attached to a carbon atom, is responsible for its reactivity. This allows it to interact with other molecules, forming esters, ethers, and various other compounds.


6-Heptyn-1-ol (CAS 63478-76-2) References

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  7. Sex pheromone of browntail moth, Euproctis chrysorrhea (L.): synthesis and field deployment.  |  Khrimian, A., et al. 2008. J Agric Food Chem. 56: 2452-6. PMID: 18333615
  8. The scope and limitations of intramolecular Nicholas and Pauson-Khand reactions for the synthesis of tricyclic oxygen- and nitrogen-containing heterocycles.  |  Closser, KD., et al. 2009. J Org Chem. 74: 3680-8. PMID: 19361191
  9. Synthesis of vinylogous amides by gold(I)-catalyzed cyclization of N-Boc-protected 6-alkynyl-3,4-dihydro-2H-pyridines.  |  Oppedisano, A., et al. 2013. J Org Chem. 78: 11007-16. PMID: 24083469
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  12. A Chemoenzymatic Strategy for Imaging Cellular Phosphatidic Acid Synthesis.  |  Bumpus, TW. and Baskin, JM. 2016. Angew Chem Int Ed Engl. 55: 13155-13158. PMID: 27633714
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Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

6-Heptyn-1-ol, 1 g

sc-483222
1 g
$36.00