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BCR160R

Fluoranthene

BCR®, certified reference material

Synonym(s):

Benzo[j,k]fluorene

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About This Item

Empirical Formula (Hill Notation):
C16H10
CAS Number:
206-44-0
Molecular Weight:
202.25
Beilstein/REAXYS Number:
1907918
EC Number:
205-912-4
MDL number:
MFCD00001184
UNSPSC Code:
41116107
PubChem Substance ID:
329773796

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

384 °C (lit.)

mp

105-110 °C (lit.)

application(s)

environmental
pharmaceutical (small molecule)

format

neat

storage temp.

2-8°C

SMILES string

c1ccc-2c(c1)-c3cccc4cccc-2c34

InChI

1S/C16H10/c1-2-8-13-12(7-1)14-9-3-5-11-6-4-10-15(13)16(11)14/h1-10H

InChI key

GVEPBJHOBDJJJI-UHFFFAOYSA-N

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Analysis Note

For more information please see:
BCR160R

Legal Information

BCR is a registered trademark of European Commission

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H302,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 2

flash_point_f

388.4 °F - closed cup

flash_point_c

198.0 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Kilian E C Smith et al.
Environmental science & technology, 46(9), 4852-4860 (2012-03-31)
Biotransformation plays a key role in hydrophobic organic compound (HOC) fate, and understanding kinetics as a function of (bio)availability is critical for elucidating persistence, accumulation, and toxicity. Biotransformation mainly occurs in an aqueous environment, posing technical challenges for producing kinetic
Sherain N Al-Subiai et al.
Mutation research, 745(1-2), 92-103 (2012-01-11)
Whilst there is growing concern over the potential detrimental impact of engineered nanoparticles (ENPs) on the natural environment, little is known about their interactions with other contaminants. In the present study, marine mussels (Mytilus sp.) were exposed for 3 days
Heidi Birch et al.
Water research, 46(18), 6002-6012 (2012-09-12)
Partitioning of fluoranthene in stormwater runoff and other urban discharges was measured by a new analytical method based on passive dosing. Samples were collected at the inlet (n = 11) and outlet (n = 8) from a stormwater retention pond in Albertslund (Denmark), and
Marie Kummerová et al.
Chemosphere, 90(2), 665-673 (2012-10-18)
Introduced organic pollutants in all ecosystem compartments can cause stress resulting in a wide range of responses including different root development. In this study, the effects of a polycyclic aromatic hydrocarbon-fluoranthene (FLT; 0.1, 1 and 7 mg L(-1)) on the
A P Rodrigues et al.
The Science of the total environment, 443, 454-463 (2012-12-12)
Fluoranthene (FLU) is a priority polycyclic aromatic hydrocarbon (PAH) commonly detected in estuarine sediments, water and biota. Despite this, information on FLU detection, accumulation and effects on marine crustaceans is scarce. This work investigated the accumulation of FLU in Carcinus
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