Benzo(k)fluoranthene - analytical standard , CAS No.207-08-9

CAS: 207-08-9 Cat. No.: B115092 Molecular Weight: 252.31 Beilstein Registry Number: 1873745 EC Number: 205-916-6
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GRADE & PURITY Analytical standard ? Analytical standard — certified-purity material for quantitative calibration. Use to prepare calibration standards and validate analytical methods.
Synonyms
UNII-U0P6LY48VF | 8,9-Benzofluoranthene | Benzo[k]fluoranthene 10 microg/mL in Cyclohexane | Benzo[k]fluoranthene, puriss., for fluorescence, >=99.0% (GC) | BIDD:ER0411 | Benzo[k]fluoranthene 10 microg/mL in Acetonitrile | J-013536 | DTXCID703909 | Dibenz
Storage
Room temperature
Shipped In
Normal
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Size
Status
Price
Qty
10mg
B115092-10mg
5

$197.90

$230.90
Save $33.00 (14.29%)
100mg
B115092-100mg
2

$1,647.90

$1,922.90
Save $275.00 (14.30%)
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Why this grade

analytical standard Analytical standard for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 11 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Overview

solubility :95% ethanol <1 mg/mL at 20 °C DMSO <1 mg/mL at 20 °C methanol <1 mg/mL at 20 °C H2O: <1 mg/mL at 20 °C acetone: soluble1-10 mg/mL at 20 °C toluene5-10 mg/mL at 20 °C
An optical sensor for nitro-aromatic compounds due to fluorescence quenching of the molecule.

Specifications

Synonyms
UNII-U0P6LY48VF | 8, 9-Benzofluoranthene | Benzo[k]fluoranthene 10 microg/mL in Cyclohexane | Benzo[k]fluoranthene, puriss., for fluorescence, >=99.0% (GC) | BIDD:ER0411 | Benzo[k]fluoranthene 10 microg/mL in Acetonitrile | J-013536 | DTXCID703909 | Dibenz
Specifications & Purity
analytical standard
Storage
Room temperature
Shipped In
Normal
Grade
Analytical standard
Names and Identifiers
Canonical SmilesC1=CC=C2C=C3C4=CC=CC5=C4C(=CC=C5)C3=CC2=C1
IUPAC Namebenzo[k]fluoranthene
InChIKeyHAXBIWFMXWRORI-UHFFFAOYSA-N
INCHI1S/C20H12/c1-2-6-15-12-19-17-10-4-8-13-7-3-9-16(20(13)17)18(19)11-14(15)5-1/h1-12H
Isomeric SMILES C1=CC=C2C=C3C4=CC=CC5=C4C(=CC=C5)C3=CC2=C1
WGK Germany 3
RTECS DF6350000
UN Number 2811
Packing Group I
Molecular Weight 252.31
Beilstein 1873745
Reaxy-Rn 1873745
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1873745&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClassNaphthalenes
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentNaphthalenes
Alternative Parents Aromatic hydrocarbons  Polycyclic hydrocarbons  Unsaturated hydrocarbons  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Naphthalene - Aromatic hydrocarbon - Polycyclic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homopolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as naphthalenes. These are compounds containing a naphthalene moiety, which consists of two fused benzene rings.
External Descriptors naphthalenes
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
VDR Tclin Vitamin D receptor (26531 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
THRB Tclin Thyroid hormone receptor beta-1 (7926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CXCL8 Tchem Interleukin-8 (642 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AHR Tclin Aryl hydrocarbon receptor (1071 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR1H4 Tclin Bile acid receptor FXR (6228 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NFKB1 Tclin Nuclear factor NF-kappa-B p105 subunit (1459 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CASP1 Tchem Caspase-1 (6235 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CASP7 Tchem Caspase-7 (3146 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TP53 Tchem Cellular tumor antigen p53 (48468 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HIF1A Tchem Hypoxia-inducible factor 1 alpha (6027 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HSD17B10 Tchem Endoplasmic reticulum-associated amyloid beta-peptide-binding protein (20669 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HPGD Tchem 15-hydroxyprostaglandin dehydrogenase [NAD+] (24926 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Associated Targets(non-human)
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
lef Anthrax lethal factor (7585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rorc Nuclear receptor ROR-gamma (89407 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mechanisms of Action
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.

7 results found

Lot NumberCertificate TypeDateItem
G2209046Certificate of AnalysisJan 19, 2026 B115092
G2502211Certificate of AnalysisJul 09, 2025 B115092
I2123082Certificate of AnalysisJun 16, 2023 B115092
G2123038Certificate of AnalysisApr 18, 2023 B115092
C2311786Certificate of AnalysisMar 24, 2023 B115092
C2311788Certificate of AnalysisMar 24, 2023 B115092
G2209047Certificate of AnalysisJul 15, 2022 B115092
Chemical and Physical Properties
Boil Point(°C)480°C
Melt Point(°C)215-218°C
Molecular Weight252.300 g/mol
XLogP36.400
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count0
Rotatable Bond Count0
Exact Mass252.094 Da
Monoisotopic Mass252.094 Da
Topological Polar Surface Area0.000 Ų
Heavy Atom Count20
Formal Charge0
Complexity338.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
References
1. Shaolin Xie, Bing Yang, Siying Li, Liangjun Ge, Min Li, Qingshi Chen, Xian Qing, Jixing Zou.  (2023)  Generation and application of a novel transgenic zebrafish line Tg(GAcyp1a:eGFP/Luc) as an in vivo assay to sensitive and specific monitoring of DLCs in the environment.  ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY,      [PMID:37729807] [10.1016/j.ecoenv.2023.115471]
2. Yuanji Gao, Hongru Feng, Bing Xia, Lei He, Congling Yang, Lijuan Zhao, Yuanjiang Pan.  (2023)  Ultrasensitive and Green Bubbling Extraction Strategies: An Extensible Solvent-Free Re-Enrichment Approach for Ultratrace Pollutants in Aqueous Samples.  ANALYTICAL CHEMISTRY,      [PMID:37624983] [10.1021/acs.analchem.3c02807]
3. Shaolin Xie, Yongyong Feng, Aiguo Zhou, Zhiyuan Lu, JixingZou.  (2023)  Comparative analysis of two new zebrafish models: The cyp1a low-expression line and cyp1a knockout line under PAHs exposure.  GENE,      [PMID:36966979] [10.1016/j.gene.2023.147391]
4. Yuan Peng, Si-Yuan He, Fang-Huan Wang, Hao-Bo Zheng, Zhe Meng.  (2022)  Determination of polycyclic aromatic hydrocarbons in edible oil by magnetic solid phase extraction based on a mesoporous molybdenum disulfide/graphite prior to gas chromatography-mass spectrometry.  MICROCHEMICAL JOURNAL,      [PMID:] [10.1016/j.microc.2022.108146]
5. Li Zhansheng, Zhao Hongxia, Li Xintong, Bekele Tadiyose Girma.  (2021)  Characteristics and sources of environmentally persistent free radicals in PM2.5 in Dalian, Northeast China: correlation with polycyclic aromatic hydrocarbons.  ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH,  29  (17): (24612-24622).  [PMID:34822091] [10.1007/s11356-021-17688-9]
6. Linfeng Chen, Xike Tian, Yong Li, Chao Yang, Yunjie Huang, Yulun Nie.  (2021)  Rapid and sensitive screening of multiple polycyclic aromatic hydrocarbons by a reusable fluorescent sensor array.  JOURNAL OF HAZARDOUS MATERIALS,      [PMID:34785436] [10.1016/j.jhazmat.2021.127694]
7. Bin Qiao, Yansong Li, Pan Hu, Yu Sun, Zhaozhao Si, Shiying Lu, Honglin Ren, Zengshan Liu, Ying Zhang, Lei Meng, Yu Zhou.  (2018)  EuNPs-MAb fluorescent probe based immunochromatographic strip for rapid and sensitive detection of fluorene.  SENSORS AND ACTUATORS B-CHEMICAL,      [PMID:] [10.1016/j.snb.2018.01.231]
8. Yong Li, Ling Long, Jing Ge, Li-xuan Yang, Jin-jin Cheng, Ling-xiang Sun, Changying Lu, Xiang-yang Yu.  (2017)  Presence, distribution and risk assessment of polycyclic aromatic hydrocarbons in rice-wheat continuous cropping soils close to five industrial parks of Suzhou, China.  CHEMOSPHERE,      [PMID:28641227] [10.1016/j.chemosphere.2017.06.055]
9. Qian Zhang, Xinyan Xu, Chenzhuo Song, Dengke Zhang, Yi Kong, Xinyi Cui.  (2024)  Effect of UV exposure and natural aging on the in vitro PAHs bioaccessibility associated with tire wear particles in soil.  SCIENCE OF THE TOTAL ENVIRONMENT,      [PMID:39197782] [10.1016/j.scitotenv.2024.175751]
10. Jiayan Shen, Long Li, Kehan Xu, Anqi Jia, Yiping Du, Huipeng Deng.  (2024)  Continuous solid-phase extraction spectroscopy and its quantification method for trace analysis.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:39549328] [10.1016/j.saa.2024.125396]
11. Xia Ling, He Yuanyuan, Xiao Xiaohua, Li Gongke.  (2019)  An online field-assisted micro-solid-phase extraction device coupled with high-performance liquid chromatography for the direct analysis of solid samples.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,  411  (18): (4073-4084).  [PMID:31025184] [10.1007/s00216-019-01809-y]
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