Date published: 2025-12-5

1-800-457-3801

SCBT Portrait Logo
Seach Input

1-Phenyl-2-propanol (CAS 698-87-3)

0.0(0)
Write a reviewAsk a question

Alternate Names:
1-Phenylpropan-2-ol; (±)-α-Methylphenethyl alcohol; (±)-1-Phenyl-2-propanol
Application:
1-Phenyl-2-propanol is a useful organic building block
CAS Number:
698-87-3
Purity:
≥97%
Molecular Weight:
136.19
Molecular Formula:
C9H12O
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

1-Phenyl-2-propanol is an alcohol that occurs naturally in various plants and flowers. This aromatic compound possesses a colorless appearance and emanates a delightful floral fragrance. Its applications extend beyond its natural occurrence, as it serves as a key component in the synthesis of other compounds and finds usage as a flavoring agent in food and beverages. The scientific research arena greatly benefits from the diverse applications of 1-Phenyl-2-propanol. It serves as a substrate for investigating enzymes such as alcohol dehydrogenase, xanthine oxidase, cytochrome P450, glutathione S-transferase, aldehyde dehydrogenase, and cytochrome b5. These enzyme studies contribute to understanding the intricate mechanisms and interactions involved in biochemical processes.


1-Phenyl-2-propanol (CAS 698-87-3) References

  1. Chemical profiling of seized methamphetamine putatively synthesized from phenylacetic acid derivatives.  |  Tsujikawa, K., et al. 2013. Forensic Sci Int. 227: 42-4. PMID: 22989601
  2. Nano-amylose-2,3-bis(3,5-dimethylphenylcarbamate)-silica hybrid sol immobilized on open tubular capillary column for capillary electrochromatography enantioseparation.  |  Sun, Y., et al. 2018. Electrophoresis. 39: 1086-1095. PMID: 29383728
  3. Enhancing cofactor recycling in the bioconversion of racemic alcohols to chiral amines with alcohol dehydrogenase and amine dehydrogenase by coupling cells and cell-free system.  |  Liu, J. and Li, Z. 2019. Biotechnol Bioeng. 116: 536-542. PMID: 30536736
  4. Kinetic Analysis as an Optimization Tool for Catalytic Esterification with a Moisture-Tolerant Zirconium Complex.  |  Villo, P., et al. 2020. J Org Chem. 85: 6959-6969. PMID: 32352291
  5. Structural Elucidation of the Mechanism of Molecular Recognition in Chiral Crystalline Sponges.  |  Zhang, SY., et al. 2020. Angew Chem Int Ed Engl. 59: 17600-17606. PMID: 32589318
  6. Py-FTIR-GC/MS Analysis of Volatile Products of Automobile Shredder Residue Pyrolysis.  |  Yang, B. and Chen, M. 2020. Polymers (Basel). 12: PMID: 33217995
  7. Site-selective reactions mediated by molecular containers.  |  Wang, R. and Yu, Y. 2022. Beilstein J Org Chem. 18: 309-324. PMID: 35368585
  8. Graphene oxide-iridium nanocatalyst for the transformation of benzylic alcohols into carbonyl compounds.  |  Chen, TR., et al. 2020. RSC Adv. 10: 4436-4445. PMID: 35495275
  9. Silica nanolayer coated capillary by hydrothermal sol-gel process for amines separation and detection of tyramine in food products.  |  Obma, A., et al. 2022. Sci Rep. 12: 7460. PMID: 35523909
  10. Porous Organic Cage-Embedded C10-Modified Silica as HPLC Stationary Phase and Its Multiple Separation Functions.  |  Wang, L., et al. 2022. Molecules. 27: PMID: 36558026
  11. Water-Soluble Pd Nanoparticles for the Anti-Markovnikov Oxidation of Allyl Benzene in Water.  |  Avila, E., et al. 2023. Nanomaterials (Basel). 13: PMID: 36678101
  12. Ligand vacancy channels in pillared inorganic-organic hybrids for electrocatalytic organic oxidation with enzyme-like activities.  |  Chen, Z., et al. 2023. Nat Commun. 14: 1184. PMID: 36864050
  13. Covalent Organic Frameworks: From Structures to Applications.  |  Tran, QN., et al. 2023. Polymers (Basel). 15: PMID: 36904520

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

1-Phenyl-2-propanol, 5 g

sc-237615
5 g
$95.00

1-Phenyl-2-propanol, 25 g

sc-237615A
25 g
$325.00