4-Methoxybiphenyl
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    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 591623

CAS#: 613-37-6

Description: 4-Methoxybiphenyl is a biochemical.


Chemical Structure

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4-Methoxybiphenyl
CAS# 613-37-6

Theoretical Analysis

MedKoo Cat#: 591623
Name: 4-Methoxybiphenyl
CAS#: 613-37-6
Chemical Formula: C13H12O
Exact Mass: 184.0888
Molecular Weight: 184.24
Elemental Analysis: C, 84.75; H, 6.57; O, 8.68

Price and Availability

Size Price Availability Quantity
5.0g USD 220.0 2 Weeks
25.0g USD 400.0 2 Weeks
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Synonym: 4-Methoxybiphenyl; NSC 3793; NSC-3793; NSC3793;

IUPAC/Chemical Name: 4-Methoxy-1,1'-biphenyl

InChi Key: RHDYQUZYHZWTCI-UHFFFAOYSA-N

InChi Code: InChI=1S/C13H12O/c1-14-13-9-7-12(8-10-13)11-5-3-2-4-6-11/h2-10H,1H3

SMILES Code: COC1=CC=C(C2=CC=CC=C2)C=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 184.24 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: Lau PL, Allen RW, Styring P. Continuous-flow Heck synthesis of 4-methoxybiphenyl and methyl 4-methoxycinnamate in supercritical carbon dioxide expanded solvent solutions. Beilstein J Org Chem. 2013 Dec 17;9:2886-97. doi: 10.3762/bjoc.9.325. eCollection 2013. PubMed PMID: 24367454; PubMed Central PMCID: PMC3869343.

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3: Glaser R, Knotts N, Wu Z, Barnes CL. Dipole Parallel-Alignment in the Crystal Structure of a Polar Biphenyl: 4'-Acetyl-4-Methoxybiphenyl (AMB). Cryst Growth Des. 2006;6(1):235-240. PubMed PMID: 19169419; PubMed Central PMCID: PMC2630165.

4: Lehmler HJ, Parkin S, Robertson LW. The three-dimensional structure of 3, 3', 5'-trichloro-4-methoxybiphenyl, a "coplanar" polychlorinated biphenyl (PCB) derivative. Chemosphere. 2002 Jan;46(3):485-8. PubMed PMID: 11829405.

5: Chandra A, Nair MG. Supercritical carbon dioxide extraction and quantification of bioactive neolignans from Magnolia virginiana flowers. Planta Med. 1995 Apr;61(2):192-5. PubMed PMID: 7753933.

6: Fry JR, Paterson P. Influence of the sulphation inhibitor, 2,6-dichloro-4-nitrophenol, on the production and conjugation, of 4-hydroxybiphenyl generated from 4-methoxybiphenyl by rat isolated hepatocytes. Biochem Pharmacol. 1987 Sep 15;36(18):3090-2. PubMed PMID: 3632729.

7: Fry JR. Influence of substrate concentration on the phase I and phase II metabolism of 4-methoxybiphenyl by rat isolated hepatocytes. Xenobiotica. 1987 Jun;17(6):751-8. PubMed PMID: 3630209.

8: Paterson P, Fry JR. Influence of cytochrome P-450 type on the pattern of conjugation of 4-hydroxybiphenyl generated from biphenyl or 4-methoxybiphenyl. Xenobiotica. 1985 Jun;15(6):493-502. PubMed PMID: 4036173.

9: Paterson P, Fry JR. The effect of ascorbic acid on the conjugation of 4-hydroxybiphenyl in rat isolated hepatocytes. Xenobiotica. 1983 Oct;13(10):607-10. PubMed PMID: 6673373.

10: Smith RV, Milton SA, Davis PJ. Microbial models of mammalian metabolism: O-dealkylation of para-alkoxybiphenyls. Appl Environ Microbiol. 1982 Jul;44(1):149-52. PubMed PMID: 6812499; PubMed Central PMCID: PMC241982.

11: Clark AM, El-Feraly FS, Li WS. Antimicrobial activity of phenolic constituents of Magnolia grandiflora L. J Pharm Sci. 1981 Aug;70(8):951-2. PubMed PMID: 7310672.

12: Fry JR. A comparison of biphenyl 4-hydroxylation and 4-methoxybiphenyl O-demethylation in rat liver microsomes. Biochem Pharmacol. 1981 Jul 15;30(14):1915-9. PubMed PMID: 7271882.

13: Maass WS, Hutzinger O. Metabolism of 4-chlorobiphenyl by lichens. Arch Environ Contam Toxicol. 1975-1976;3(4):470-8. PubMed PMID: 816260.

14: Bridges JW, Creaven PJ, Williams RT. The fluorescence of some biphenyl derivatives. Biochem J. 1965 Sep;96(3):872-8. PubMed PMID: 5862424; PubMed Central PMCID: PMC1207230.