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CRM48641

Supelco

Naphthalene solution

certified reference material, 200 μg/mL in methanol

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About This Item

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

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

SMILES string

c1ccc2ccccc2c1

InChI

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

InChI key

UFWIBTONFRDIAS-UHFFFAOYSA-N

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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_germany

WGK 1

flash_point_f

49.5 °F - closed cup

flash_point_c

9.7 °C - closed cup

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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
John B Morris
Toxicology, 309, 66-72 (2013-04-27)
Naphthalene vapor is a nasal cytotoxicant in the rat and mouse but is a nasal carcinogen in only the rat. Inhalation dosimetry is a critical aspect of the inhalation toxicology of inspired vapors and may contribute to the species differences
Azusa Suzuki et al.
Bioorganic & medicinal chemistry letters, 23(3), 886-892 (2013-01-01)
We synthesized various C8-naphthylethynylated 2'-deoxyadenosine derivatives and investigated their photophysical properties. Among them, cyano- and N,N-dimethylamino-substituted 8-naphthylethynylated 2'-deoxyadenosine derivatives ((cn)A and (dn)A) showed strong fluorescence with high quantum yields and a remarkable solvatofuorochromicity. In particular, fluorescence of N,N-dimethylamino-substituted (2,6dn)A was
K Vijayavel et al.
Biomedical and environmental sciences : BES, 26(4), 295-302 (2013-03-29)
To investigate protective effect of Coleus aromaticus leaf extract against naphthalene induced hepatotoxicity in rats. Eighteen male rats were divided into three groups. Group I rats were treated as control. Group II rats were intraperitoneally administered with naphthalene (435 mg/kg
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