Interesting facts
              Interesting Facts about 1-phenylpropan-1-ol
1-phenylpropan-1-ol, a fascinating compound in organic chemistry, captures attention due to its unique structure and diverse applications. Here are some intriguing aspects of this compound:
- Structure: This compound features a propanol backbone with a phenyl group attached, leading to a notable presence of both aromatic and aliphatic elements. This combination contributes to its distinct chemical properties.
 - Occurrence: You might find 1-phenylpropan-1-ol in nature as a component of various essential oils. Its presence in fragrant compounds highlights its potential for use in the fragrance and flavor industries.
 - Synthetic Applications: 1-phenylpropan-1-ol serves as a valuable intermediate in the synthesis of other organic compounds, including pharmaceuticals and agrochemicals, making it an important compound for study in medicinal chemistry.
 - Hydrophobicity: The compound's hydrophobic character allows it to interact favorably with lipophilic environments, making it a subject of interest for formulations involving non-aqueous solvents.
 - Safety Considerations: As with many organic compounds, researchers emphasize the importance of safe handling practices when working with 1-phenylpropan-1-ol. Proper laboratory protocols should always be maintained to ensure safety.
 
In summary, 1-phenylpropan-1-ol stands out not only for its interesting chemical structure but also for its diverse uses and significance across various fields of science. It illustrates the beauty and complexity of organic compounds and their multifaceted roles in both nature and industry.
Synonyms
          1-Phenyl-1-propanol
          1-Phenylpropan-1-ol
          93-54-9
          Phenylpropanol
          Phenycholon
          1-Phenylpropanol
          Fepar
          Ejibil
          Felicur
          Livonal
          Bilergon
          Carbicol
          Epatoxfen
          Felitrope
          Gallenperlen
          Phenicol
          Phenychol
          Phenylchol
          Choleda
          Unichol
          1-Phenylpropyl alcohol
          Phenyl ethyl carbinol
          Phenylcholon
          alpha-Ethylbenzyl alcohol
          Ethyl phenyl carbinol
          1-Propanol, 1-phenyl-
          1-Phenyl-1-hydroxypropane
          Phenylpropanol [JAN]
          Phenylaethylcarbinol
          alpha-Ethylbenzenemethanol
          FEMA No. 2884
          SH 261
          alpha-Hydroxypropylbenzene
          Benzenemethanol, .alpha.-ethyl-
          .alpha.-Ethylbenzyl alcohol
          Phenylaethylcarbinol [German]
          Benzenemethanol, alpha-ethyl-
          NSC 25504
          phenyl propanol
          BENZYL ALCOHOL, alpha-ETHYL-
          EINECS 202-256-0
          Ethylbenzyl alcohol
          NSC-25504
          BRN 1906759
          Benzyl alcohol, .alpha.-ethyl-
          DTXSID2044474
          Phenylpropanol (JAN)
          AI3-19819
          0F897O3O4M
          1-Phenyl-propan-1-ol
          MFCD00004564
          .alpha.-Hydroxypropylbenzene
          .omega.-Ethylbenzyl alcohol
          PHENYLPROPANOL [MART.]
          DTXCID0024474
          EC 202-256-0
          4-06-00-03183 (Beilstein Handbook Reference)
          ETHYLBENZYL ALCOHOL [WHO-DD]
          1-PHENYL-1-PROPANOL [FHFI]
          NCGC00165972-01
          .ALPHA.-ETHYLBENZYL ALCOHOL [MI]
          Fenicol (VAN)
          PHENYLPROPANOL (MART.)
          ETHYLPHENYLCARBINOL
          a-ethylbenzyl alcohol
          R-(+)-1-Phenylpropanol
          S-(-)-1-Phenylpropanol
          (R)-1-phenyl-1-propanol
          1Phenylpropanol
          UNII-0F897O3O4M
          1Phenylpropan1ol
          Phenylpropylalkohol
          1Propanol, 1phenyl
          1-Phenyl-n-propanol
          1Phenylpropyl alcohol
          a-Hydroxypropylbenzene
          1Phenyl1hydroxypropane
          Other proprietary names
          alphaEthylbenzenemethanol
          alphaEthylbenzyl alcohol
          alphaHydroxypropylbenzene
          omegaEthylbenzyl alcohol
          1- phenyl-1-propanol
          Phenyl-1-propan-1-ol
          alpha-Ethyl-benzyl alcohol
          Benzyl alcohol, alphaethyl
          1-hydroxy-1-phenylpropane
          Benzenemethanol, alphaethyl
          (+/-)-1-Phenylpropanol
          .alpha.-Ethylbenzenemethanol
          a-Ethylbenzenemethanol, 9CI
          SCHEMBL56673
          ghl.PD_Mitscher_leg0.415
          PHENYLPROPANOL [INCI]
          (+/-) 1-phenyl-1-propanol
          CHEMBL1397202
          CHEBI:31995
          FEMA 2884
          DTXSID30273982
          1-Phenyl-1-propanol, >=97%
          DTXCID901777798
          AAA09354
          NSC25504
          NSC41708
          STR02714
          Benzenemethanol, alpha-ethyl-(9CI)
          Tox21_112275
          NSC-41708
          1-Phenyl-1-propanol, >=97%, FG
          AKOS000249117
          AKOS016843880
          AB88253
          CS-W013334
          HY-W012618
          CAS-93-54-9
          s11247
          NCGC00165972-02
          NCGC00165980-01
          NCGC00166078-01
          DA-66667
          SY020321
          SY101126
          DB-043324
          DB-072950
          NS00004787
          P0212
          D01470
          EN300-128217
          SBI-0654040.0001
          SR-01000944521
          ( inverted exclamation markA)-1-Phenyl-1-propanol
          SR-01000944521-1
          Q15726117
          Z335245178
          202-256-0
          215-621-4
          258-889-8
              
Solubility of 1-Phenylpropan-1-ol
1-Phenylpropan-1-ol, with the chemical formula C9H12O, exhibits intriguing solubility characteristics that reflect its molecular structure.
General Solubility Behavior
This compound is primarily soluble in organic solvents due to the presence of the hydrophobic phenyl group. However, its solubility can vary based on the following factors:
It's crucial to note that solubility is a key factor when considering the use of 1-phenylpropan-1-ol in various applications, as it may influence the behavior of the compound in biochemical and industrial environments.
Summary
In conclusion, while 1-phenylpropan-1-ol demonstrates a favorable solubility profile in non-polar and moderate polar solvents, its low solubility in water reflects its organic nature, marking its significance in the realm of organic chemistry.