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2-Fluorobiphenyl - 98%, high purity , CAS No.321-60-8

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2-Fluorobiphenyl - 98%, high purity , CAS No.321-60-8

3 Citations

COA

Grade & Purity:

≥98%

Cas Number: 321-60-8
Molecular Weight: 172.2
Beilstein Registry Number: 2043175
EC Number: 206-290-7
MDL number: MFCD00000317
PubChem CID: 67579
PubChem SID: 488183953

In stock

Item Number

F103594

Grouped product items
SKU	Size	Availability	Price
F103594-1g	1g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$20.90
F103594-5g	5g	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$80.90
F103594-10g	10g	3	$123.90
F103594-25g	25g	3	$237.90
F103594-100g	100g	2	$855.90

View related series

Non heterocyclic fluorine-containing block (1408) Synthetic block (741)

Basic Description

Synonyms	Tox21_202912 \| NSC10366 \| NSC-10366 \| KLECYOQFQXJYBC-UHFFFAOYSA- \| Biphenyl, 2-fluoro- \| F0265 \| 1-fluoro-2-phenylbenzene \| 2-Fluorobiphenyl \| 2-Fluoro-biphenyl \| DTXCID5027728 \| C12H9F \| CAS-321-60-8 \| W-106853 \| ortho-Fluorodiphenyl \| 10.14272/KLECYOQFQ
Specifications & Purity	≥98%
Shipped In	Normal
Product Description	2-Fluorobiphenyl is a white to off white powder. It is catabolized by C. elegans, yielding hydroxylated products. The metabolism of 2-fluorobiphenyl by hepatic microsomes isolated from control and aroclor 1254-treated rats and pigeons was studied. 2-Fluorobiphenyl was used as an internal standard for analysis of environmental pollutants in sediments using pressurized liquid extraction and gas chromatography-mass spectrometry. It was used to study the solvent dynamics of 1,2,4,5-tetracyanobenzene/biphenyl derivative radical ion pairs by picosecond absorption spectroscopy. It was also used as a sole carbon and energy source for the biphenyl-degrading bacterium Pseudomonas pseudoalcaligenes KF707.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Biphenyls and derivatives

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Biphenyls and derivatives
Intermediate Tree Nodes	Not available
Direct Parent	Biphenyls and derivatives
Alternative Parents	Fluorobenzenes Aryl fluorides Organofluorides Hydrofluorocarbons Hydrocarbon derivatives
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Biphenyl - Halobenzene - Fluorobenzene - Aryl halide - Aryl fluoride - Hydrofluorocarbon - Hydrocarbon derivative - Organofluoride - Organohalogen compound - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as biphenyls and derivatives. These are organic compounds containing to benzene rings linked together by a C-C bond.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488183953
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488183953
IUPAC Name	1-fluoro-2-phenylbenzene
INCHI	InChI=1S/C12H9F/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9H
InChIKey	KLECYOQFQXJYBC-UHFFFAOYSA-N
Smiles	C1=CC=C(C=C1)C2=CC=CC=C2F
Isomeric SMILES	C1=CC=C(C=C1)C2=CC=CC=C2F
WGK Germany	3
UN Number	3077
Packing Group	III
Molecular Weight	172.2
Beilstein	2043175
Reaxy-Rn	2043175
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2043175&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

12 results found

Lot Number	Certificate Type	Date	Item
H2126208	Certificate of Analysis	Jun 11, 2025	F103594
J2418687	Certificate of Analysis	Jun 22, 2024	F103594
J2418688	Certificate of Analysis	Jun 22, 2024	F103594
J2418689	Certificate of Analysis	Jun 22, 2024	F103594
C2506502	Certificate of Analysis	Jun 22, 2024	F103594
F2210604	Certificate of Analysis	May 31, 2022	F103594
F2210603	Certificate of Analysis	May 31, 2022	F103594
F2210566	Certificate of Analysis	May 31, 2022	F103594
F2210600	Certificate of Analysis	May 31, 2022	F103594
F2210567	Certificate of Analysis	May 31, 2022	F103594
G2313127	Certificate of Analysis	May 31, 2022	F103594
C1828133	Certificate of Analysis	Jan 27, 2022	F103594

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Chemical and Physical Properties

Solubility	Soluble in alcohol, ether. Insoluble in water.
Boil Point(°C)	248°C
Melt Point(°C)	73-76°C
Molecular Weight	172.200 g/mol
XLogP3	4.000
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	1
Exact Mass	172.069 Da
Monoisotopic Mass	172.069 Da
Topological Polar Surface Area	0.000 Å²
Heavy Atom Count	13
Formal Charge	0
Complexity	149.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. Hong-Xue Qi,Hui-Zhen Li,Ping Ma,Jing You. (2015-05-26) Integrated sediment quality assessment through biomarker responses and bioavailability measurements: Application in Tai Lake, China.. Ecotoxicology and environmental safety, 119 (148-154).
2. Zhang YueYue, Tang Dingliang, Wu Yuanfei, Huang Xiaojia. (2025) Facile and rapid preparation of fluorinated imprinted adsorbent for magnetic solid phase extraction of liquid–crystal monomers. MICROCHIMICA ACTA, 192 (1): (1-13).
3. Timur Meng, Xianhao Liu, Yuyue Peng, Hongliang Lei, Zhiyi Li, Saowaluk Chaleawlert-umpon, Yutong Dai, Kaige Zhao, Lina Li. (2024) Fluorine Incorporation for Enhanced Gas Separation Performance in Porous Organic Polymers: Investigating Reaction Pathways and Pore Structure Control. ACS Applied Materials & Interfaces, 16 (30): (40190-40198).

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