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48566

苊烯

Name: 苊烯
Brand: SUPELCO
Price: 3138.99 CNY

analytical standard

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10 MG

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10 MG

¥3,138.99

About This Item

经验公式（希尔记法）:

C₁₂H₈

CAS号:

208-96-8

分子量:

152.19

Beilstein:

774092

EC 号:

205-917-1

MDL编号:

MFCD00003806

UNSPSC代码:

12352200

PubChem化学物质编号:

24872113

¥3,138.99

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Acenaphthylene may be used as an analytical reference standard for the determination of the analyte in water using gas chromatography-flame ionization detection (GC-FID).[1]

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

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GHS07

警示用语：

Warning

危险声明

H302,H315,H319,H335

预防措施声明

P261 - P264 - P271 - P301 + P312 - P302 + P352 - P305 + P351 + P338

危险分类

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

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

251.6 °F - closed cup

闪点(°C)

122.0 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

技术规格说明书

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Determination of organic compounds in water using dispersive liquid-liquid microextraction.

Rezaee M, et al.

Journal of Chromatography A, 1116(1-2), 1-9 (2006)

Ring current effects in crystals. Evidence from 13C chemical shift tensors for intermolecular shielding in 4,7-di-t-butylacenaphthene versus 4,7-di-t-butylacenaphthylene.

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

Isolation and characterization of genes encoding polycyclic aromatic hydrocarbon dioxygenase from acenaphthene and acenaphthylene degrading Sphingomonas sp. strain A4.

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

The effect of ethynyl substitution and cyclopenta fusion on the ultraviolet absorption spectra of polycyclic aromatic hydrocarbons.

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

Simultaneous monitoring of profiles of polycyclic aromatic hydrocarbons in contaminated air with semipermeable membrane devices and spruce needles.

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

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59305U SUPELCOGEL^™ Ca，6% 交联，HPLC 色谱柱	59320U SUPELCOGEL^™ C610H, 6%交联HPLC柱	59318U SUPELCOGEL^™ 6%交联HPLC柱	59335U SUPELCOGEL^™ Pb，6% 交联， HPLC 色谱柱
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separation technique ligand exchange	separation technique ion exclusion	separation technique ligand exchange	separation technique ligand exchange
agency suitable for USP L19	agency suitable for USP L17	agency -	agency suitable for USP L34
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product line SUPELCOGEL^™	product line SUPELCOGEL^™	product line SUPELCOGEL^™	product line SUPELCOGEL^™
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苊烯

analytical standard

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WGK

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