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Acenaphthylene

certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

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About This Item

Fórmula empírica (Notação de Hill):
C12H8
Número CAS:
208-96-8
Peso molecular:
152.19
Beilstein:
774092
Número CE:
205-917-1
Número MDL:
MFCD00003806
Código UNSPSC:
41116107
ID de substância PubChem:
329770136
NACRES:
NA.24

grau

certified reference material
TraceCERT®

Nível de qualidade

300

linha de produto

TraceCERT®

prazo de validade

limited shelf life, expiry date on the label

fabricante/nome comercial

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

pb

280 °C (lit.)

pf

78-82 °C (lit.)
89-92 °C

densidade

0.899 g/mL at 25 °C (lit.)

aplicação(ões)

environmental

formato

neat

temperatura de armazenamento

2-8°C

cadeia de caracteres SMILES

c1cc2C=Cc3cccc(c1)c23

InChI

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

chave InChI

HXGDTGSAIMULJN-UHFFFAOYSA-N

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Descrição geral

This certified reference material (CRM) is produced and certified in accordance with ISO/IEC 17025 and ISO 17034. This CRM is traceable to primary material from an NMI, e.g. NIST or NMIJ.
Certified content by quantitative NMR incl. uncertainty and expiry date are given on the certificate.
Download your certificate at: http://www.sigma-aldrich.com.

Aplicação

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

Embalagem

Bottomless glass bottle. Contents are inside inserted fused cone.

Informações legais

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

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H302,H315,H319,H335

Classificações de perigo

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

Órgãos-alvo

Respiratory system

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

251.6 °F - closed cup

Ponto de fulgor (°C)

122.0 °C - closed cup

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Certificados de análise (COA)

Lot/Batch Number
BCCB9535
BCBR2490V
BCBP9893V
BCBL7004V
BCBD3103V

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

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Xiuhua Zhu et al.
Environmental pollution (Barking, Essex : 1987), 156(2), 461-466 (2008-03-04)
Gaseous emissions of combusted electronic scrap, PVC, carpet and wood were monitored for polycyclic aromatic hydrocarbons (PAHs) by simultaneous use of semipermeable membrane devices (SPMDs) and shoots of spruce needles (Picea abies). It was found that phenanthrene, acenaphthylene and fluorene
Ling Zi Sang et al.
Talanta, 78(4-5), 1339-1344 (2009-04-14)
A fluorimetric method for simultaneous determination of dissolved acenaphthylene (Ace) phenanthrene (Ph) and pyrene (Py), mixed in an aqueous mineral salts medium (MSM), was developed. The linear ranges for determination of Ace, Ph and Py dissolved in the mixture were
N D Marsh et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 56A(8), 1499-1511 (2000-07-25)
We have examined the UV spectra of six newly-synthesized ethynyl-PAH (1-ethynylnaphthalene, 5-ethynylacenaphthylene, 1-ethynylanthracene, 9-ethynylphenanthrene, 3-ethynylfluoranthene, and 1-ethynylpyrene) and five corresponding CP-PAH (acenaphthylene, aceanthrylene, acephenanthrylene, cyclopenta[cd]fluoranthene, and cyclopenta[cd]pyrene) and have found the following systematic behavior: ethynyl-substitution results in average bathochromic shifts
Onruthai Pinyakong et al.
FEMS microbiology letters, 238(2), 297-305 (2004-09-11)
Sphingomonas sp. strain A4 is capable of utilizing acenaphthene and acenaphthylene as sole carbon and energy sources, but it is unable to grow on other polycyclic aromatic hydrocarbons (PAHs). The genes encoding terminal oxygenase components of ring-hydroxylating dioxygenase (arhA1 and
Zhiru Ma et al.
The journal of physical chemistry. A, 111(10), 2020-2027 (2007-03-29)
13C chemical shift tensor data from 2D FIREMAT spectra are reported for 4,7-di-t-butylacenaphthene and 4,7-di-t-butylacenaphthylene. In addition, calculations of the chemical shielding tensors were completed at the B3LYP/6-311G** level of theory. While the experimental tensor data on 4,7-di-t-butylacenaphthylene are in
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