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Merck
CN

CRM48641

Naphthalene solution

certified reference material, 200 μg/mL in methanol

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About This Item

CAS Number:
91-20-3
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329798455
MDL number:
MFCD00001742
Beilstein/REAXYS Number:
7822574

Key Documents

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SMILES string

c1ccc2ccccc2c1

InChI key

UFWIBTONFRDIAS-UHFFFAOYSA-N

InChI

1S/C10H8/c1-2-6-10-8-4-3-7-9(10)5-1/h1-8H

grade

certified reference material, TraceCERT®

product line

TraceCERT®

CofA

current certificate can be downloaded

packaging

ampule of 1 mL

concentration

200 μg/mL in methanol

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

application(s)

cleaning products
cosmetics
environmental
food and beverages
personal care

format

single component solution

storage temp.

2-30°C

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General description

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Legal Information

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

target_organs

Eyes

Storage Class

3 - Flammable liquids

wgk

WGK 1

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup

Regulatory Information

危险化学品
This item has

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Isabel Brunet-Galmés et al.
Journal of bacteriology, 194(23), 6642-6643 (2012-11-13)
Pseudomonas stutzeri AN10 (CCUG 29243) can be considered a model strain for aerobic naphthalene degradation. We report the complete genome sequence of this bacterium. Its 4.71-Mb chromosome provides insights into other biodegradative capabilities of strain AN10 (i.e., benzoate catabolism) and
Arpita Panja et al.
Bioorganic & medicinal chemistry letters, 23(3), 893-896 (2012-12-26)
Aryl-naphthalene diacetates prepared from bispropargyl sulfones, ethers and amines via Garratt-Braverman Cyclization have been selectively hydrolysed by AK lipase to the monoacetates 12a-c in high yields. The regioisomeric mono acetates 13a-c have been prepared by acetylation of the corresponding diols
Nicola A Colabufo et al.
Bioorganic & medicinal chemistry, 21(5), 1324-1332 (2013-01-26)
Substituted naphthalenyl derivatives bearing oxazole, or thiazole or furyl heteronuclei have been carried out as bioisosters of aryl-oxazoles and -thiazoles derivatives previously reported in order to investigate the role of the hindrance on the activity towards P-gp/BCRP/and MRP1 transporters. In
Dickson Y S Yan et al.
Environmental pollution (Barking, Essex : 1987), 178, 15-22 (2013-03-26)
The effectiveness and mechanisms of naphthalene and metal removal from artificially contaminated soil by FeEDTA/FeEDDS-activated persulfate were investigated through batch experiments. Using FeEDTA-activated persulfate, higher naphthalene removal from the soil at 7 h was achieved (89%), compared with FeEDDS-activated persulfate (75%).
Xu-Liang Cao et al.
Journal of food protection, 75(12), 2163-2171 (2012-12-06)
A method based on isotope dilution headspace solid-phase microextraction, followed by gas chromatography and mass spectrometry, was developed for the determination of naphthalene in foods. Optimum method sensitivity was achieved by the addition of NaCl in water at saturation and
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