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92549

Supelco

苊烯

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

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About This Item

經驗公式（希爾表示法）:
C12H8
CAS號碼:
208-96-8
分子量：:
152.19
Beilstein:
774092
EC號碼:
205-917-1
MDL號碼:
MFCD00003806
分類程式碼代碼:
41116107
PubChem物質ID:
329770136
NACRES:
NA.24

等級

certified reference material
TraceCERT®

品質等級

300

產品線

TraceCERT®

儲存期限

limited shelf life, expiry date on the label

製造商／商標名

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

技術

HPLC: suitable
gas chromatography (GC): suitable

bp

280 °C (lit.)

mp

78-82 °C (lit.)
89-92 °C

密度

0.899 g/mL at 25 °C (lit.)

應用

environmental

形式

neat

儲存溫度

2-8°C

SMILES 字串

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 密鑰

HXGDTGSAIMULJN-UHFFFAOYSA-N

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相關類別

一般說明

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.

應用

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

包裝

Bottomless glass bottle. Contents are inside inserted fused cone.

法律資訊

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

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類（WGK）

WGK 3

閃點（°F）

251.6 °F - closed cup

閃點（°C）

122.0 °C - closed cup

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分析證明 (COA)

Lot/Batch Number

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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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