36734
酞酰亚胺
PESTANAL®, analytical standard
别名:
邻苯二甲酰亚胺
等级
analytical standard
质量水平
产品线
PESTANAL®
保质期
limited shelf life, expiry date on the label
技术
HPLC: suitable
gas chromatography (GC): suitable
mp
232-235 °C (lit.)
应用
agriculture
environmental
包装形式
neat
SMILES字符串
O=C1NC(=O)c2ccccc12
InChI
1S/C8H5NO2/c10-7-5-3-1-2-4-6(5)8(11)9-7/h1-4H,(H,9,10,11)
InChI key
XKJCHHZQLQNZHY-UHFFFAOYSA-N
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应用
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
其他说明
Ion Mobility: TWCCSN2 value of 124.9 Å2 [M+H]+ and 124.0 Å2 [M-H]-
The collision cross section (CCS) measurement was provided by Waters Corporation, using the SYNAPT XS mass spectrometer.
For a description and overview of how ion mobility enables the measurement of the CCS of an ion visit ims.waters.com.
Further information on the SYNAPT XS mass spectrometer can be found on the IMS microsite and product webpage.
TWCCS measurements are expected to be within 2% of this reference value.
P/N 36734 is part of the Waters Extractables & Leachables UNIFI scientific library which can be downloaded from Waters Marketplace.
The collision cross section (CCS) measurement was provided by Waters Corporation, using the SYNAPT XS mass spectrometer.
For a description and overview of how ion mobility enables the measurement of the CCS of an ion visit ims.waters.com.
Further information on the SYNAPT XS mass spectrometer can be found on the IMS microsite and product webpage.
TWCCS measurements are expected to be within 2% of this reference value.
P/N 36734 is part of the Waters Extractables & Leachables UNIFI scientific library which can be downloaded from Waters Marketplace.
法律信息
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
储存分类代码
11 - Combustible Solids
WGK
WGK 1
闪点(°F)
302.0 °F - closed cup
闪点(°C)
150 °C - closed cup
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
危险化学品
此项目有
Supramolecular chemistry: Reading polymer codes.
Ken D Shimizu
Nature chemistry, 2(8), 612-613 (2010-07-24)
Hülya Akgün et al.
Bioorganic & medicinal chemistry, 20(13), 4149-4154 (2012-05-29)
Structurally modified phthalimide derivatives were prepared through condensation of phthalic and tetrafluorophthalic anhydride with selected sulfonamides with variable yields. All compounds were screened for their antimycobacterium activity against Mycobacterium tuberculosis H37Ra (ATCC 25177) using a micro broth dilution technique. The
Abhishek A Kantak et al.
Journal of the American Chemical Society, 133(49), 19960-19965 (2011-10-21)
The development of a novel intermolecular oxidative amination reaction, a synthetic transformation that involves the simultaneous functionalization of both a N-H and C-H bond, is described. The process, which is mediated by an I(III) oxidant and contains no metal catalysts
Baocun Zhu et al.
Organic & biomolecular chemistry, 8(7), 1650-1654 (2010-03-20)
A highly selective ratiometric fluorescent probe, which contains an aminonaphthalimide fluorophore and a self-immolative spacer for 1,4-dithiothreitol (DTT) detection was designed and synthesized. The probe displays a 66 nm red-shift of fluorescence emission and the color changes from colorless to
Ellane J Park et al.
Langmuir : the ACS journal of surfaces and colloids, 28(29), 10934-10941 (2012-07-04)
There is considerable current interest in developing methods to integrate nanoparticles into optical, electronic, and biological systems due to their unique size-dependent properties and controllable shape. We report herein a versatile new approach for covalent immobilization of nanoparticles onto substrates
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