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    Chemistry

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    Also known as: 2-methoxyphenol, 90-05-1, O-methoxyphenol, 2-hydroxyanisole, Phenol, 2-methoxy-, Guaiastil
    Molecular Formula
    C7H8O2
    Molecular Weight
    124.14  g/mol
    InChI Key
    LHGVFZTZFXWLCP-UHFFFAOYSA-N
    FDA UNII
    6JKA7MAH9C
    Guaiacol
    An agent thought to have disinfectant properties and used as an expectorant. (From Martindale, The Extra Pharmacopoeia, 30th ed, p747)
    1 2D Structure

    Guaiacol

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    2-methoxyphenol
    2.1.2 InChI
    InChI=1S/C7H8O2/c1-9-7-5-3-2-4-6(7)8/h2-5,8H,1H3
    2.1.3 InChI Key
    LHGVFZTZFXWLCP-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    COC1=CC=CC=C1O
    2.2 Other Identifiers
    2.2.1 UNII
    6JKA7MAH9C
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. 2-hydroxy-anisole

    2. 2-hydroxyanisole

    3. 2-methoxy-phenol

    4. 2-methoxyphenol

    5. Catechol, Methyl

    6. Guaicol

    7. Methyl Catechol

    2.3.2 Depositor-Supplied Synonyms

    1. 2-methoxyphenol

    2. 90-05-1

    3. O-methoxyphenol

    4. 2-hydroxyanisole

    5. Phenol, 2-methoxy-

    6. Guaiastil

    7. Pyroguaiac Acid

    8. O-guaiacol

    9. O-hydroxyanisole

    10. Pyrocatechol Monomethyl Ether

    11. 1-hydroxy-2-methoxybenzene

    12. Methylcatechol

    13. Anastil

    14. Guaicol

    15. Phenol, O-methoxy-

    16. Guaicolina

    17. Guajol

    18. Guasol

    19. O-methyl Catechol

    20. Catechol Monomethyl Ether

    21. Creosote, Wood

    22. Methoxyphenol

    23. Guajakol

    24. Creodon

    25. 8021-39-4

    26. Wood Creosote

    27. 2-methoxy-phenol

    28. Hydroxyanisole

    29. Fema No. 2532

    30. Guaiacol [jan]

    31. Methylcatachol

    32. Ortho-guaiacol

    33. 2-methoxy Phenol

    34. Nsc 3815

    35. (mu)-methoxyphenol

    36. Mfcd00002185

    37. Guaiacol (jan)

    38. Creodon (tn)

    39. Nsc-3815

    40. 2-methoxyl-4-vinylphenol

    41. 6jka7mah9c

    42. 9009-62-5

    43. 2-methoxyphenol (guaiacol)

    44. Chembl13766

    45. Chebi:28591

    46. Phenol, 2-methoxy-, Homopolymer

    47. Phenol, Methoxy-

    48. Ncgc00090827-02

    49. Ncgc00090827-04

    50. Guajacol

    51. Dsstox_cid_3113

    52. Dsstox_rid_76880

    53. Guajakol [czech]

    54. Dsstox_gsid_23113

    55. Creosote, Beechwood

    56. Guaiacol (natural)

    57. Pyrocatechol Methyl Ester

    58. Cas-90-05-1

    59. 26247-00-7

    60. Ccris 2943

    61. Guaiacol [jan:nf]

    62. Hsdb 4241

    63. Sr-01000838056

    64. Einecs 201-964-7

    65. Unii-6jka7mah9c

    66. Guiacol

    67. Creasote

    68. Methoxy Phenol

    69. 6-methoxyphenol

    70. Hydroxyl Anisole

    71. Ai3-05615

    72. Nat.guaiacol

    73. O-methylcatechol

    74. O-guiacol

    75. O--methoxyphenol

    76. Orthomethoxyphenol

    77. O-methoxy-phenol

    78. 2-methyloxyphenol

    79. Ortho-methoxyphenol

    80. Guaiacol,(s)

    81. Jz3

    82. 2-(methyloxy)phenol

    83. Guaiacol [fhfi]

    84. Guaiacol [hsdb]

    85. Guaiacol [mi]

    86. Guaiacol [vandf]

    87. Catechol Mono Methyl Ether

    88. Guaiacol [mart.]

    89. Bmse000436

    90. Bmse010027

    91. Guaiacol [usp-rs]

    92. Guaiacol [who-dd]

    93. Ec 201-964-7

    94. Guaiacol, Puriss., 99%

    95. Wln: Qr Bo1

    96. Dsstox_rid_77552

    97. 1- Hydroxy-2-methoxybenzene

    98. 3-methoxy-4-hydroxy Benzene

    99. Dsstox_gsid_24853

    100. Schembl21626

    101. Ghl.pd_mitscher_leg0.900

    102. Guaiacol (liquid) Extra Pure

    103. Guaiacol, Oxidation Indicator

    104. Mls001055375

    105. Guaiacol [ep Monograph]

    106. Guaiacol [usp Impurity]

    107. Dtxsid0023113

    108. Nsc3815

    109. Guaiacol, Natural, >=99%, Fg

    110. Hms2089d18

    111. Hms2233p04

    112. Hms3372n11

    113. Hms3715e11

    114. Pharmakon1600-01506165

    115. A Hydroxlyated Aryl Lignin Fragment

    116. Bcp27082

    117. Cs-d1347

    118. Hy-n1380

    119. Str03604

    120. Tox21_111031

    121. Tox21_201136

    122. Tox21_202990

    123. Tox21_400004

    124. Bdbm50240369

    125. Nsc760376

    126. S3872

    127. Stl281868

    128. Zinc13512224

    129. Akos000118831

    130. Ccg-214035

    131. Db11359

    132. Nsc-760376

    133. Pb43791

    134. Ps-3252

    135. Guaiacol, Saj First Grade, >=98.0%

    136. Ncgc00090827-01

    137. Ncgc00090827-03

    138. Ncgc00090827-05

    139. Ncgc00090827-06

    140. Ncgc00090827-07

    141. Ncgc00258688-01

    142. Ncgc00260535-01

    143. Ac-34997

    144. Guaiacol, Vetec(tm) Reagent Grade, 98%

    145. Smr000059155

    146. Sy048708

    147. Cas-8021-39-4

    148. Db-024854

    149. Ft-0626815

    150. Ft-0671312

    151. Guaifenesin Impurity A [ep Impurity]

    152. M0121

    153. C01502

    154. D00117

    155. F70227

    156. 2-methoxyphenol;o-methoxyphenol;2-hydroxyanisole

    157. Ab00876226-06

    158. Ab00876226_07

    159. A843426

    160. Q412403

    161. Q-100002

    162. Sr-01000838056-2

    163. Sr-01000838056-3

    164. F2173-0425

    165. Guaiacol, European Pharmacopoeia (ep) Reference Standard

    166. Guaiacol, United States Pharmacopeia (usp) Reference Standard

    167. Guaiacol, Pharmaceutical Secondary Standard; Certified Reference Material

    2.4 Create Date
    2005-03-25
    3 Chemical and Physical Properties
    Molecular Weight 124.14 g/mol
    Molecular Formula C7H8O2
    XLogP31.3
    Hydrogen Bond Donor Count1
    Hydrogen Bond Acceptor Count2
    Rotatable Bond Count1
    Exact Mass124.052429494 g/mol
    Monoisotopic Mass124.052429494 g/mol
    Topological Polar Surface Area29.5 Ų
    Heavy Atom Count9
    Formal Charge0
    Complexity83
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count1
    4 Drug and Medication Information
    4.1 Therapeutic Uses

    IT IS USED EMPIRICALLY AS AN EXPECTORANT TO LESSEN AMT OF MUCOUS IN THE CHRONIC STAGES OF BRONCHITIS & BRONCHIECTASIS. IT IS FREQUENTLY PRESCRIBED FOR ITS STIMULANT EXPECTORANT ACTION AS A CONSTITUENT OF A STEAM INHALANT. THE ANTISEPTIC ACTION IS WEAK & NOT CLINICALLY USEFUL. ... IT HAS BEEN EMPLOYED AS A LOCAL ANESTHETIC IN DENTISTRY, IN A MANNER SIMILAR TO THYMOL. IT IS OCCASIONALLY EMPLOYED EXTERNALLY FOR ITS DISINFECTANT ACTION.

    Osol, A. and J.E. Hoover, et al. (eds.). Remington's Pharmaceutical Sciences. 15th ed. Easton, Pennsylvania: Mack Publishing Co., 1975., p. 1102

    MEDICATION (VET): TOPICALLY (1.0-1.5%), IN UDDER AND WOUND TREATMENT OINTMENTS & IN POULTICES; WHEN ELIMINATED BY RESP MUCOUS MEMBRANES, SLIGHT ANTISEPTIC & LOCAL ANESTHETIC EFFECTS MAY OCCUR. INTERNALLY ... USED IN ANTIFERMENT & ANTIBLOAT MIXTURES.

    Rossoff, I.S. Handbook of Veterinary Drugs. New York: Springer Publishing Company, 1974., p. 144

    ANTIPYRETIC; STYPTIC; ASTRINGENT

    Clayton, G. D. and F. E. Clayton (eds.). Patty's Industrial Hygiene and Toxicology: Volume 2A, 2B, 2C: Toxicology. 3rd ed. New York: John Wiley Sons, 1981-1982., p. 2601

    MEDICATION (VET): PARASITICIDE, DEODORANT

    Budavari, S. (ed.). The Merck Index - Encyclopedia of Chemicals, Drugs and Biologicals. Rahway, NJ: Merck and Co., Inc., 1989., p. 403

    Disinfectants; Expectorants

    National Library of Medicine's Medical Subject Headings online file (MeSH, 1999)

    Medication (Vet): ... Oral or parenteral mucolytic antiseptic antitussive in bronchopneumonias. ... Inhalant. In antiphlogistic, anodyne liquids on congested udders, in horse leg paints, and in poultices. Spray over tail biting swine to ... discourage cannibalism. Parenteral /dosage/ in camphorated oil. US mfr use 50 mg/mL concentration.

    Rossoff, I.S. Handbook of Veterinary Drugs. New York: Springer Publishing Company, 1974., p. 249

    For the symptomatic relief of coughs associated with colds, bronchial catarrh, influenza and upper respiratory tract infections such as laryngitis and pharyngitis. Codeine is a well-known centrally acting cough suppressant. Guaiacol acts as an expectorant, loosening bronchial secretions in the respiratory tract. /Guaiacol, codeine combination/

    Datapharm Communications Ltd; Electronic Medicines Compendium (eMC), Summary of Product Characteristics (SPC) for Pulmo Bailly (Last updated February 2010). Available from, as of March 9, 2010: https://emc.medicines.org.uk/medicine/22147/SPC/Pulmo+Bailly/

    4.2 Drug Warning

    THE REPEATED ABSORPTION OF THERAPEUTIC DOSES FROM GASTROENTERIC TRACT MAY INDUCE SIGNS OF CHRONIC INTOXICATION, CHARACTERIZED BY DISTURBANCES OF VISION & DIGESTION (INCR PERISTALSIS & EXCRETION OF BODY FECES). IN ISOLATED CASES OF "SELF-MEDICATION", HYPERTENSION & ALSO GENERAL CARDIOVASCULAR COLLAPSE HAVE BEEN DESCRIBED.

    Clayton, G. D. and F. E. Clayton (eds.). Patty's Industrial Hygiene and Toxicology: Volume 2A, 2B, 2C: Toxicology. 3rd ed. New York: John Wiley Sons, 1981-1982., p. 2603

    WHEREVER CREOSOTE IS INDICATED FOR INTERNAL MEDICATION CREOSOTE FROM WOOD TAR SHOULD BE DISPENSED & UNDER NO CIRCUMSTANCES SHOULD CREOSOTE FROM COAL TAR BE GIVEN, UNLESS EXPLICITLY SO DIRECTED.

    The Merck Index. 10th ed. Rahway, New Jersey: Merck Co., Inc., 1983., p. 368

    Do not use in Cats.

    Budavari, S. (ed.). The Merck Index - Encyclopedia of Chemicals, Drugs and Biologicals. Rahway, NJ: Merck and Co., Inc., 1989., p. 403

    4.3 Drug Indication

    It is used medicinally as an expectorant, antiseptic, and local anesthetic. Guaiacol is used in traditional dental pulp sedation, and has the property of inducing cell proliferation; guaiacol is a potent scavenger of reactive oxygen radicals and its radical scavenging activity may be associated with its effect on cell proliferation.

    5 Pharmacology and Biochemistry
    5.1 Absorption, Distribution and Excretion

    Absorption

    In rats, guaiacol is rapidly absorbed, being present in the blood 5 minutes after oral administration, and reaching its peak plasma concentration in about 10 minutes. Its elimination from the blood is usually as rapid.

    Route of Elimination

    Excreted by rabbits in combined form with sulfate (15%) and glucuronic acid (72%).

    CREOSOTE IS RAPIDLY ABSORBED FROM THE GASTROENTERIC TRACT AND THROUGH THE SKIN. IT APPEARS TO BE EXCRETED IN THE URINE MAINLY IN CONJUGATION WITH SULFURIC, HEXURONIC, & OTHER ACIDS. OXIDATION ALSO OCCURS WITH THE FORMATION OF CMPD THAT IMPART A SMOKY APPEARANCE TO THE URINE. TRACES ARE EXCRETED BY WAY OF THE LUNGS.

    Clayton, G. D. and F. E. Clayton (eds.). Patty's Industrial Hygiene and Toxicology: Volume 2A, 2B, 2C: Toxicology. 3rd ed. New York: John Wiley Sons, 1981-1982., p. 2603

    Medical experience indicates that toxic quantities can be absorbed through the skin quite readily.

    Clayton, G. D. and F. E. Clayton (eds.). Patty's Industrial Hygiene and Toxicology: Volume 2A, 2B, 2C: Toxicology. 3rd ed. New York: John Wiley Sons, 1981-1982., p. 2525

    Methoxyphenol largely absorbed from digestive tract and stored in blood, kidneys, and respiratory organs. Excreted by rabbits in combined form with sulfate (15%) and glucuronic acid (72%).

    National Research Council. Drinking Water & Health Volume 1. Washington, DC: National Academy Press, 1977., p. 740

    In rats, guaiacol is rapidly absorbed, being present in the blood 5 minutes after oral administration, and reaching its peak plasma concentration in about 10 minutes. Its elimination from the blood is usually as rapid.

    Datapharm Communications Ltd; Electronic Medicines Compendium (eMC), Summary of Product Characteristics (SPC) for Pulmo Bailly (Last updated February 2010). Available from, as of March 9, 2010: https://emc.medicines.org.uk/medicine/22147/SPC/Pulmo+Bailly/

    5.2 Metabolism/Metabolites

    .../IT APPEARS TO BE CONJUGATED/ WITH SULFURIC, HEXURONIC & OTHER ACIDS. OXIDATION...OCCURS WITH FORMATION OF COMPOUNDS THAT IMPART A SMOKY APPEARANCE TO THE URINE.

    Clayton, G. D. and F. E. Clayton (eds.). Patty's Industrial Hygiene and Toxicology: Volume 2A, 2B, 2C: Toxicology. 3rd ed. New York: John Wiley Sons, 1981-1982., p. 2603

    Several strains of Aspergillus niger hydroxylated anisole to give o-hydroxyanisole as main product.

    Bocks SM; Phytochemistry 6 (6): 785 (1967)

    o-Methoxyphenol yields 3-methoxycatechol probably in rabbit; yields o-methoxyphenyl sulfate probably in rabbit. o-Methoxyphenol yields catechol in rat; yields 1,2-dimethoxybenzene in mouse, rabbit, guinea pig, and rat. /From table/

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POLYMERS","supplierCountry":"CHINA","foreign_port":"SHANGHAI","customer":"GRANULES INDIA LIMITED","customerCountry":"INDIA","quantity":"16000.00","actualQuantity":"16000","unit":"KGS","unitRateFc":"4","totalValueFC":"65556.4","currency":"USD","unitRateINR":"340.2","date":"31-Aug-2024","totalValueINR":"5443976","totalValueInUsd":"65556.4","indian_port":"Madras Sea","hs_no":"29095010","bill_no":"5355256","productDescription":"API","marketType":"REGULATED MARKET","country":"CHINA","selfForZScoreResived":"Pharma Grade","supplierPort":"SHANGHAI","supplierAddress":"PACIFIC PTE. LTD., 1 BIOPOLIS DRIVE#03-04 AMNIOS, SINGAPORE 138622SDNF SG","customerAddress":"SECOND FLOOR, BLOCK-III,MY HOME HUB"}]
    01-Jan-2021
    31-Aug-2024
    KGS
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    Average Price (USD/KGS)

    Number of Transactions

    Total Quantity (KGS)

    Total Value (USD)

    Quantity (KGS) & Unit rate (USD/KGS) over time

    API Imports and Exports

    Importing Country Total Quantity
    (KGS)    		 Average Price
    (USD/KGS)    		 Number of Transactions

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