3-Hydroxyanisole
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MedKoo CAT#: 591693

CAS#: 150-19-6

Description: 3-Hydroxyanisole is a biochemical.


Chemical Structure

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3-Hydroxyanisole
CAS# 150-19-6

Theoretical Analysis

MedKoo Cat#: 591693
Name: 3-Hydroxyanisole
CAS#: 150-19-6
Chemical Formula: C7H8O
Exact Mass: 124.0524
Molecular Weight: 124.14
Elemental Analysis: C, 67.73; H, 6.50; O, 25.78

Price and Availability

Size Price Availability Quantity
25.0g USD 220.0 2 Weeks
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Synonym: 3-Hydroxyanisole; NSC 21735; NSC-21735; NSC21735

IUPAC/Chemical Name: 3-Methoxyphenol

InChi Key: ASHGTJPOSUFTGB-UHFFFAOYSA-N

InChi Code: InChI=1S/C7H8O2/c1-9-7-4-2-3-6(8)5-7/h2-5,8H,1H3

SMILES Code: OC1=CC=CC(OC)=C1

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >2 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

Preparing Stock Solutions

The following data is based on the product molecular weight 124.14 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL

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Reconstitution Calculator

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1: Rahman MM, Hussain MM, Asiri AM. Fabrication of 3-methoxyphenol sensor based on Fe3O4 decorated carbon nanotube nanocomposites for environmental safety: Real sample analyses. PLoS One. 2017 Sep 22;12(9):e0177817. doi: 10.1371/journal.pone.0177817. eCollection 2017. PubMed PMID: 28938019; PubMed Central PMCID: PMC5609863.

2: Foti MC, Daquino C, DiLabio GA, Ingold KU. A meta effect in nonphotochemical processes: the homolytic chemistry of m-methoxyphenol. J Org Chem. 2008 Mar 21;73(6):2408-11. doi: 10.1021/jo702520r. Epub 2008 Feb 23. PubMed PMID: 18294001.

3: Vargas AC, Quiclet-Sire B, Zard SZ. Total synthesis of 10-norparvulenone and of O-methylasparvenone using a xanthate-mediated free radical addition-cyclization sequence. Org Lett. 2003 Oct 2;5(20):3717-9. PubMed PMID: 14507213.

4: Moridani MY, Cheon SS, Khan S, O'Brien PJ. Metabolic activation of 3-hydroxyanisole by isolated rat hepatocytes. Chem Biol Interact. 2003 Jan 6;142(3):317-33. PubMed PMID: 12453669.

5: Engelmann T, Kaufmann F, Diekert G. Isolation and characterization of a veratrol:corrinoid protein methyl transferase from Acetobacterium dehalogenans. Arch Microbiol. 2001 May;175(5):376-83. PubMed PMID: 11409548.

6: Fenoll LG, Rodríguez-López JN, Varón R, García-Ruiz PA, García-Cánovas F, Tudela J. Action mechanism of tyrosinase on meta- and para-hydroxylated monophenols. Biol Chem. 2000 Apr;381(4):313-20. PubMed PMID: 10839460.

7: Fenoll LG, Rodríguez-López JN, Varón R, García-Ruiz PA, García-Cánovas F, Tudela J. Kinetic study of the oxidation of 3-hydroxyanisole catalysed by tyrosinase. Biophys Chem. 2000 Feb 14;84(1):65-76. PubMed PMID: 10723545.

8: Rizk PN, Hanzlik RP. Oxidative and non-oxidative metabolism of 4-iodoanisole by rat liver microsomes. Xenobiotica. 1995 Feb;25(2):143-50. PubMed PMID: 7618342.