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Merck

92549

Supelco

アセナフチレン

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

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About This Item

実験式(ヒル表記法):
C12H8
CAS番号:
分子量:
152.19
Beilstein:
774092
EC Number:
MDL番号:
UNSPSCコード:
41116107
PubChem Substance ID:
NACRES:
NA.24

グレード

certified reference material
TraceCERT®

品質水準

製品種目

TraceCERT®

シェルフライフ

limited shelf life, expiry date on the label

メーカー/製品名

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

テクニック

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.)

アプリケーション

environmental

フォーマット

neat

保管温度

2-8°C

SMILES記法

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 Key

HXGDTGSAIMULJN-UHFFFAOYSA-N

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詳細

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.

アプリケーション

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

包装

底の開いたガラス瓶内容物は内部に挿入され接着された円錐部に入っています。

法的情報

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

ピクトグラム

Exclamation mark

シグナルワード

Warning

危険有害性情報

危険有害性の分類

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

ターゲットの組織

Respiratory system

保管分類コード

11 - Combustible Solids

WGK

WGK 3

引火点(°F)

251.6 °F - closed cup

引火点(℃)

122.0 °C - closed cup


適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

労働安全衛生法名称等を表示すべき危険物及び有害物

名称等を表示すべき危険物及び有害物

労働安全衛生法名称等を通知すべき危険物及び有害物

名称等を通知すべき危険物及び有害物

Jan Code

92549-100MG:
92549-50MG:
92549-BULK:
92549-1G:
92549-VAR:


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試験成績書(COA)

Lot/Batch Number

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文書ライブラリにアクセスする

Eldra Delannay et al.
Journal of chromatography. A, 1127(1-2), 45-51 (2006-06-30)
Nowadays, centrifugal partition chromatography (CPC) separations can be routinely achieved at the laboratory scale. The solvent system selection has been made easy, as generic sets of solvent systems are described in publications and books. This approach, however, generally reduces the
F J Rivas et al.
Journal of hazardous materials, 75(1), 89-98 (2000-06-01)
Removal of acenaphthylene from water has been carried out by means of different treatments combining UV radiation, ozone and hydrogen peroxide. Ozonation alone or in conjunction with hydrogen peroxide (10(-3) M) resulted in the highest elimination rates. Thus, conversions as
Fabienne Reisen et al.
Environmental science & technology, 36(20), 4302-4311 (2002-10-22)
Acenaphthene and acenaphthylene are polycyclic aromatic hydrocarbons (PAHs) emitted into the atmosphere from a variety of incomplete combustion sources such as diesel exhaust. Both PAHs are present in the gas phase under typical atmospheric conditions and therefore can undergo atmospheric
Siriwat Poonthrigpun et al.
Applied and environmental microbiology, 72(9), 6034-6039 (2006-09-08)
The acenaphthylene-degrading bacterium Rhizobium sp. strain CU-A1 was isolated from petroleum-contaminated soil in Thailand. This strain was able to degrade 600 mg/liter acenaphthylene completely within three days. To elucidate the pathway for degradation of acenaphthylene, strain CU-A1 was mutagenized by
Yan Hao et al.
Organic & biomolecular chemistry, 10(4), 724-728 (2011-12-15)
A simple and novel protocol for the efficient synthesis of a series of 8-carboxylnaphthyl functionalized pyrazolo[3,4-b]pyridine derivatives was developed through a one-pot, three-component reaction involving acenaphthylene-1,2-dione and 1H-pyrazol-5-amine in acetic acid medium. The reaction represents the first facile conversion of

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