Quaterphenyl

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

MedKoo CAT#: 531315

CAS#: 1166-18-3

Description: Quaterphenyl is a bioactive chemical.

Chemical Structure

img
Quaterphenyl
CAS# 1166-18-3
Instruction

Theoretical Analysis

MedKoo Cat#: 531315
Name: Quaterphenyl
CAS#: 1166-18-3
Chemical Formula: C24H18
Exact Mass: 306.14
Molecular Weight: 306.408
Elemental Analysis: C, 94.08; H, 5.92

Price and Availability

This product is not in stock, which may be available by custom synthesis. For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge). Quote less than 1g will not be provided. To request quote, please email to sales @medkoo.com or click below button.
Note: Price will be listed if it is available in the future.

Request quote for custom synthesis

Synonym: Quaterphenyl

IUPAC/Chemical Name: m-Quaterphenyl (8CI)

InChi Key: OWPJBAYCIXEHFA-UHFFFAOYSA-N

InChi Code: InChI=1S/C24H18/c1-3-9-19(10-4-1)21-13-7-15-23(17-21)24-16-8-14-22(18-24)20-11-5-2-6-12-20/h1-18H

SMILES Code: C1(C2=CC=CC(C3=CC=CC(C4=CC=CC=C4)=C3)=C2)=CC=CC=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: >3 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

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 306.41 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
Formulation protocol:
In vitro protocol:
In vivo protocol:

Molarity Calculator

Calculate the mass, volume, or concentration required for a solution.
=
x
x
g/mol

*When preparing stock solutions always use the batch-specific molecular weight of the product found on the vial label and SDS / CoA (available online).

Reconstitution Calculator

The reconstitution calculator allows you to quickly calculate the volume of a reagent to reconstitute your vial. Simply enter the mass of reagent and the target concentration and the calculator will determine the rest.

=
÷

Dilution Calculator

Calculate the dilution required to prepare a stock solution.
x
=
x

1: Yan JF, Zhong GH, Wang RS, Zhang K, Lin HQ, Chen X. Superconductivity and Phase Stability of Potassium-Intercalated p-Quaterphenyl. J Phys Chem Lett. 2018 Nov 25. doi: 10.1021/acs.jpclett.8b03263. [Epub ahead of print] PubMed PMID: 30472837.

2: Burkhard LP, Lahren T, Highland TL, Hockett JR, Mount DR, Norberg-King TJ. Bioaccumulation of Highly Hydrophobic Chemicals by Lumbriculus variegatus. Arch Environ Contam Toxicol. 2019 Jan;76(1):129-141. doi: 10.1007/s00244-018-0554-6. Epub 2018 Aug 27. PubMed PMID: 30151657.

3: Zhu C, Poater A, Duhayon C, Kauffmann B, Saquet A, Maraval V, Chauvin R. Carbo-biphenyls and Carbo-terphenyls: Oligo(phenylene ethynylene) Ring Carbo-mers. Angew Chem Int Ed Engl. 2018 May 14;57(20):5640-5644. doi: 10.1002/anie.201713411. Epub 2018 Apr 23. PubMed PMID: 29504656.

4: Tomsej T, Horak J, Tomsejova S, Krpec K, Klanova J, Dej M, Hopan F. The impact of co-combustion of polyethylene plastics and wood in a small residential boiler on emissions of gaseous pollutants, particulate matter, PAHs and 1,3,5- triphenylbenzene. Chemosphere. 2018 Apr;196:18-24. doi: 10.1016/j.chemosphere.2017.12.127. Epub 2017 Dec 21. PubMed PMID: 29289847.

5: Zhou X, Bebensee F, Yang M, Bebensee R, Cheng F, He Y, Shen Q, Shang J, Liu Z, Besenbacher F, Linderoth TR, Wu K. Steering Surface Reaction at Specific Sites with Self-Assembly Strategy. ACS Nano. 2017 Sep 26;11(9):9397-9404. doi: 10.1021/acsnano.7b04900. Epub 2017 Aug 17. PubMed PMID: 28809530.

6: Dänekamp B, Kobin B, Bhattacharyya S, Hecht S, Milián-Medina B, Gierschner J. Tuning of the electronic and photophysical properties of ladder-type quaterphenyl by selective methylene-bridge fluorination. Phys Chem Chem Phys. 2016 Jun 28;18(24):16501-8. doi: 10.1039/c6cp02045c. Epub 2016 Jun 6. PubMed PMID: 27263988.

7: Winkler A. Initial stages of organic film growth characterized by thermal desorption spectroscopy. Surf Sci. 2015 Jul 2;643:124-137. PubMed PMID: 26778860; PubMed Central PMCID: PMC4712358.

8: Jungbauer SH, Schindler S, Herdtweck E, Keller S, Huber SM. Multiple Multidentate Halogen Bonding in Solution, in the Solid State, and in the (Calculated) Gas Phase. Chemistry. 2015 Sep 21;21(39):13625-36. doi: 10.1002/chem.201502043. Epub 2015 Sep 2. Erratum in: Chemistry. 2015 Oct 26;21(44):15467. PubMed PMID: 26331633.

9: Shang J, Wang Y, Chen M, Dai J, Zhou X, Kuttner J, Hilt G, Shao X, Gottfried JM, Wu K. Assembling molecular Sierpiński triangle fractals. Nat Chem. 2015 May;7(5):389-93. doi: 10.1038/nchem.2211. Epub 2015 Mar 30. PubMed PMID: 25901816.

10: Snyder JA, Bragg AE. Structural control of nonadiabatic bond formation: the photochemical formation and stability of substituted 4a,4b-dihydrotriphenylenes. J Phys Chem A. 2015 Apr 30;119(17):3972-85. doi: 10.1021/acs.jpca.5b01749. Epub 2015 Apr 21. PubMed PMID: 25849258.

11: Sun Q, Zhang C, Cai L, Tan Q, Xu W. Oxygen-induced self-assembly of quaterphenyl molecules on metal surfaces. Chem Commun (Camb). 2014 Oct 18;50(81):12112-5. doi: 10.1039/c4cc05235h. PubMed PMID: 25171326.

12: Herbrich S, Gericke KH, Smolin AG, Vasyutinskii OS. Two-color two-photon excited fluorescence of 2-methyl-5-tert-butyl-p-quaterphenyl (DMQ): ab initio calculations and experimental determination of the molecular parameters. J Phys Chem A. 2014 Jul 17;118(28):5248-55. doi: 10.1021/jp505251c. Epub 2014 Jul 7. PubMed PMID: 24964069.

13: Kuwahara S, Nakamura M, Yamaguchi A, Ikeda M, Habata Y. Combination of a new chiroptical probe and theoretical calculations for chirality detection of primary amines. Org Lett. 2013 Nov 15;15(22):5738-41. doi: 10.1021/ol402767a. Epub 2013 Oct 30. PubMed PMID: 24171647.

14: Kadadevarmath JS, Malimath GH, Melavanki RM, Patil NR. Static and dynamic model fluorescence quenching of laser dye by carbon tetrachloride in binary mixtures. Spectrochim Acta A Mol Biomol Spectrosc. 2014 Jan 3;117:630-4. doi: 10.1016/j.saa.2013.08.053. Epub 2013 Sep 6. PubMed PMID: 24113015.

15: Kawasaki G, Yoshitomi I, Yanamoto S, Yamada S, Mizuno A, Umeda M. Pigmentation of the oral mucosa by PCB poisoning in Yusho patients. Arch Oral Biol. 2013 Sep;58(9):1260-4. doi: 10.1016/j.archoralbio.2013.04.008. Epub 2013 May 22. PubMed PMID: 23706593.

16: Kuwahara S, Chamura R, Tsuchiya S, Ikeda M, Habata Y. Chirality transcription and amplification by [2]pseudorotaxanes. Chem Commun (Camb). 2013 Mar 18;49(22):2186-8. doi: 10.1039/c2cc38758a. PubMed PMID: 23318978.

17: Fu GL, Zhang HY, Yan YQ, Zhao CH. p-Quaterphenyls laterally substituted with a dimesitylboryl group: a promising class of solid-state blue emitters. J Org Chem. 2012 Feb 17;77(4):1983-90. doi: 10.1021/jo202574n. Epub 2012 Feb 2. PubMed PMID: 22260452.

18: Yasutake D, Ashizuka Y, Hori T, Kurokawa Y, Kajiwara J, Hirata T, Ishiguro Y, Iida T, Uchi H, Furue M. [The rapid analysis of polychlorinated quaterphenyls in blood using different diameter capillary column with the high-resolution gas chromatograph high-resolution mass spectrometer]. Fukuoka Igaku Zasshi. 2011 Apr;102(4):145-52. Japanese. PubMed PMID: 21706895.

19: Russell JC, Blunt MO, Garfitt JM, Scurr DJ, Alexander M, Champness NR, Beton PH. Dimerization of tri(4-bromophenyl)benzene by aryl-aryl coupling from solution on a gold surface. J Am Chem Soc. 2011 Mar 30;133(12):4220-3. doi: 10.1021/ja110837s. Epub 2011 Mar 3. PubMed PMID: 21370872.

20: Gu Z, Feng J, Han W, Wu M, Fu J, Sheng G. Characteristics of organic matter in PM2.5 from an e-waste dismantling area in Taizhou, China. Chemosphere. 2010 Aug;80(7):800-6. doi: 10.1016/j.chemosphere.2010.04.078. Epub 2010 May 26. PubMed PMID: 20510434.