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Key Documents

40053

Supelco

Naphthalene solution

certified reference material, 5000 μg/mL in methanol

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About This Item

CAS Number:
Beilstein:
7822574
EC Number:
MDL number:
UNSPSC Code:
41116105
PubChem Substance ID:

grade

certified reference material
TraceCERT®

product line

TraceCERT®

CofA

current certificate can be downloaded

packaging

ampule of 1 mL

concentration

5000 μg/mL in methanol

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

agriculture
cleaning products
cosmetics
environmental
food and beverages
personal care

format

single component solution

storage temp.

2-8°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

Gene Information

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General description

Sigma-Aldrich offers an extensive line of Fluka and Supelco brand neats and single-component solutions for a variety of applications that include, but are not limited to, environmental, food and beverage, forensics, petrochemical and pharmaceutical analyses. Naphthalene solution may be prepared, via dissolving polycyclic aromatic hydrocarbons in methanol.

Application

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

Other Notes

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.

Legal Information

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

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

51.8 °F - closed cup

Flash Point(C)

11 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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Quantitative SERS sensors for environmental analysis of naphthalene
Peron.O, et al.
Analyst, 135, 1018-1022 (2011)
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
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
Kaori Yamaguchi et al.
Journal of chromatography. A, 1288, 149-154 (2013-03-26)
Hydro gel formed by 5'-guanosine monophosphate (GMP) in the presence of a potassium ion is expected to exhibit interesting selectivity in capillary electrophoretic separations. Here, we estimated the conditional association constants between the hydro gel (G-gel) and aromatic compounds by

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