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48566

Acenaphthylene

analytical standard

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About This Item

Empirical Formula (Hill Notation):
C12H8
CAS Number:
208-96-8
Molecular Weight:
152.19
EC Number:
205-917-1
UNSPSC Code:
12352200
PubChem Substance ID:
24872113
Beilstein/REAXYS Number:
774092
MDL number:
MFCD00003806
NACRES:
NA.24
Technical Service
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grade

analytical standard

Quality Level

100

CofA

current certificate can be downloaded

packaging

ampule of 100 mg

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

bp

280 °C (lit.)

mp

78-82 °C (lit.)

density

0.899 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

storage temp.

2-30°C

SMILES string

c1cc2C=Cc3cccc(c1)c23

InChI

1S/C12H8/c1-3-9-4-2-6-11-8-7-10(5-1)12(9)11/h1-8H

InChI key

HXGDTGSAIMULJN-UHFFFAOYSA-N

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Acenaphthylene may be used as an analytical reference standard for the determination of the analyte in water using  gas chromatography-flame ionization detection (GC-FID).

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

flash_point_f

251.6 °F - closed cup

flash_point_c

122.0 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

208-96-8

CAS No.

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Certificates of Analysis (COA)

Lot/Batch Number
LRAD7846
LRAC8729
LRAD3627
LC25926V
LC25389V

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Determination of organic compounds in water using dispersive liquid-liquid microextraction.
Rezaee M, et al.
Journal of Chromatography A, 1116(1-2), 1-9 (2006)
Yan Hao et al.
Organic & biomolecular chemistry, 10(4), 724-728 (2011-12-15)
A simple and novel protocol for the efficient synthesis of a series of 8-carboxylnaphthyl functionalized pyrazolo[3,4-b]pyridine derivatives was developed through a one-pot, three-component reaction involving acenaphthylene-1,2-dione and 1H-pyrazol-5-amine in acetic acid medium. The reaction represents the first facile conversion of
E Leonhardt et al.
Analytical chemistry, 70(6), 1228-1230 (1998-04-08)
Polycyclic aromatic hydrocarbons were extracted from a soil sample using ultrasound and dichloromethane-, cyclohexane-, and toluene-water mixtures. It was found that when dichloromethane is used as an extractant, acenaphthylene reacts with the solvent. Several chlorinated and oxygenated derivatives were identified.
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