Please Wait
Applying Filters...
menu
    • menu
    Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.

    Virtual Booth

    Contact Supplier

    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

    Virtual Booth

    Contact Supplier

    xyz-pharma-m-2024-10-07

    Virtual Booth

    Contact Supplier

    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

    Virtual Booth

    Contact Supplier

    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

    Virtual Booth

    Contact Supplier

    xyz-pharma-m-2024-10-07

    Virtual Booth

    Contact Supplier

    Menu

    2-(4-Hydroxyphenyl)Ethanol

    ACTIVE PHARMA INGREDIENTS

    PharmaCompass
    $ API Ref.Price (USD/KG) : 76Xls

    Filters

    clear-filterReset all filters
    2D Structure
    Also known as: Tyrosol, 501-94-0, 4-hydroxyphenethyl alcohol, 4-(2-hydroxyethyl)phenol, 4-hydroxyphenylethanol, 4-hydroxybenzeneethanol
    Molecular Formula
    C8H10O2
    Molecular Weight
    138.16  g/mol
    InChI Key
    YCCILVSKPBXVIP-UHFFFAOYSA-N
    FDA UNII
    1AK4MU3SNX
    Tyrosol is a metabolite found in or produced by Saccharomyces cerevisiae.
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    4-(2-hydroxyethyl)phenol
    2.1.2 InChI
    InChI=1S/C8H10O2/c9-6-5-7-1-3-8(10)4-2-7/h1-4,9-10H,5-6H2
    2.1.3 InChI Key
    YCCILVSKPBXVIP-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    C1=CC(=CC=C1CCO)O
    2.2 Other Identifiers
    2.2.1 UNII
    1AK4MU3SNX
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. 2-(4-hydroxyphenyl)ethyl Acetate

    2. 4-hydroxybenzeneethanol

    3. 4-hydroxyphenylethanol

    4. Beta-(4-hydroxyphenyl)ethanol

    5. N-tyrosol

    6. P-hydroxyphenylethanol

    7. P-tyrosol

    8. Para-hydroxyphenylethanol

    9. Tyrosol

    10. Tyrosol Acetate

    2.3.2 Depositor-Supplied Synonyms

    1. Tyrosol

    2. 501-94-0

    3. 4-hydroxyphenethyl Alcohol

    4. 4-(2-hydroxyethyl)phenol

    5. 4-hydroxyphenylethanol

    6. 4-hydroxybenzeneethanol

    7. P-hydroxyphenethyl Alcohol

    8. Benzeneethanol, 4-hydroxy-

    9. P-tyrosol

    10. 4-hydroxyphenylethyl Alcohol

    11. 2-(4-hydroxyphenyl)ethyl Alcohol

    12. P-thyrosol

    13. Mfcd00002902

    14. Nsc 59876

    15. 2-(p-hydroxyphenyl)ethanol

    16. Metoprolol Impurity 07

    17. 4-hydroxy-benzeneethanol

    18. 1ak4mu3snx

    19. P-hydroxyphenylethyl Alcohol

    20. 4-(2-hydroxy-ethyl)-phenol

    21. Chembl53566

    22. Chebi:1879

    23. Nsc-59876

    24. P-hydroxyphenylethanol

    25. Tyrosol C

    26. Smr000857159

    27. P-hpea

    28. 4-hydroxyphenethylalcohol

    29. Einecs 207-930-8

    30. Unii-1ak4mu3snx

    31. Beta-(4-hydroxyphenyl)ethanol

    32. 4-tyrosol

    33. Yrl

    34. Tyrosol ,(s)

    35. 4-hydroxybenzenethanol

    36. 4-(hydroxyethyl)phenol

    37. P-hydroxy-benzeneethanol

    38. Tyrosol [mi]

    39. B-(p-hydroxyphenyl)ethanol

    40. Bmse000173

    41. B-(4-hydroxyphenyl)ethanol

    42. 4-hydroxyphenylmethylcarbinol

    43. 2-(p-hydroxyphenyl) Ethanol

    44. Schembl43838

    45. (4-hydroxyphenethyl) Alcohol

    46. 2-(4-hydroxyphenyl) Ethanol

    47. 2-(4-hydroxyphenyl)-ethanol

    48. Beta-(p-hydroxyphenyl)ethanol

    49. Mls001332423

    50. Mls001332424

    51. Phenethyl Alcohol, P-hydroxy-

    52. Ethanol, 2-(4-hydroxyphenyl)

    53. Dtxsid8060111

    54. Schembl10620528

    55. .beta.-(p-hydroxyphenyl)ethanol

    56. 2-(4-hydroxyphenyl)-1-ethanol

    57. Ethanol, 2-(4-hydroxyphenyl)-

    58. .beta.-(4-hydroxyphenyl)ethanol

    59. Hms2230e12

    60. Zinc164581

    61. 2-(4-hydroxyphenyl)ethanol, 98%

    62. Bcp34277

    63. Hy-n0474

    64. Nsc59876

    65. Str02735

    66. Hydroxyphenethyl Alcohol, P-

    67. Bdbm50339585

    68. S3773

    69. Akos000280287

    70. Ac-2493

    71. Ccg-266147

    72. Cs-w019782

    73. Ks-5274

    74. Ncgc00246994-01

    75. Sy001653

    76. Db-019455

    77. Am20060146

    78. Ft-0608647

    79. H0720

    80. N1496

    81. A14486

    82. C06044

    83. 2-(4-hydroxyphenyl)ethanol, Analytical Standard

    84. Nsc 59876; P-hpea;4-hydroxyphenethyl Alcohol

    85. Q402607

    86. Metoprolol Tartrate Impurity G [ep Impurity]

    87. Metoprolol Succinate Impurity G [ep Impurity]

    88. Tyrosol (constituent Of Rhodiola Rosea) [dsc]

    89. F0001-1309

    90. 947d0361-23c6-4863-8346-22ab05108ac5

    91. 4-hydroxy-benzeneethanol;4-hydroxyphenylethanol;beta-(4-hydroxyphenyl)ethanol

    2.4 Create Date
    2005-03-26
    3 Chemical and Physical Properties
    Molecular Weight 138.16 g/mol
    Molecular Formula C8H10O2
    XLogP30.4
    Hydrogen Bond Donor Count2
    Hydrogen Bond Acceptor Count2
    Rotatable Bond Count2
    Exact Mass138.068079557 g/mol
    Monoisotopic Mass138.068079557 g/mol
    Topological Polar Surface Area40.5 Ų
    Heavy Atom Count10
    Formal Charge0
    Complexity85.3
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count1
    4 Pharmacology and Biochemistry
    4.1 MeSH Pharmacological Classification

    Anti-Arrhythmia Agents

    Agents used for the treatment or prevention of cardiac arrhythmias. They may affect the polarization-repolarization phase of the action potential, its excitability or refractoriness, or impulse conduction or membrane responsiveness within cardiac fibers. Anti-arrhythmia agents are often classed into four main groups according to their mechanism of action: sodium channel blockade, beta-adrenergic blockade, repolarization prolongation, or calcium channel blockade. (See all compounds classified as Anti-Arrhythmia Agents.)

    Antioxidants

    Naturally occurring or synthetic substances that inhibit or retard oxidation reactions. They counteract the damaging effects of oxidation in animal tissues. (See all compounds classified as Antioxidants.)