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Merck
CN

88060

氯化四苯磷

for the spectrophotometric det. of Bi, Co, ≥97.0%

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关于此项目

线性分子式:
(C6H5)4P(Cl)
化学文摘社编号:
分子量:
374.84
EC Number:
217-890-3
UNSPSC Code:
12352200
PubChem Substance ID:
Beilstein/REAXYS Number:
3922393
MDL number:
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产品名称

氯化四苯磷, for the spectrophotometric det. of Bi, Co, ≥97.0%

InChI key

WAGFXJQAIZNSEQ-UHFFFAOYSA-M

InChI

1S/C24H20P.ClH/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24;/h1-20H;1H/q+1;/p-1

SMILES string

[Cl-].c1ccc(cc1)[P+](c2ccccc2)(c3ccccc3)c4ccccc4

assay

≥97.0% (AT)
≥97.0%

form

crystals

quality

for the spectrophotometric det. of Bi, Co

technique(s)

UV/Vis spectroscopy: suitable

mp

272-274 °C (lit.)

Quality Level

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存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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Denice C Bay et al.
Biochimica et biophysica acta, 1798(3), 526-535 (2009-12-29)
Escherichia coli multidrug resistance protein E (EmrE) is a four transmembrane alpha-helix protein, and a member of the small multidrug resistance protein family that confers resistance to a broad range of quaternary cation compounds (QCC) via proton motive force. The
Myocardial imaging for mitochondrial membrane potential.
H William Strauss et al.
JACC. Cardiovascular imaging, 5(3), 293-296 (2012-03-17)
Yang Zhou et al.
Bioconjugate chemistry, 22(8), 1459-1472 (2011-06-24)
Alteration in mitochondrial transmembrane potential (ΔΨ(m)) is an important characteristic of cancer. The observation that the enhanced negative mitochondrial potential is prevalent in tumor cell phenotype provides a conceptual basis for development of mitochondrion-targeting therapeutic drugs and molecular imaging probes.
Do Kyun Kim et al.
Journal of microbiology and biotechnology, 23(3), 430-435 (2013-03-07)
Multidrug resistance, especially multidrug efflux mechanisms that extrude structurally unrelated cytotoxic compounds from the cell by multidrug transporters, is a serious problem and one of the main reasons for the failure of therapeutic treatment of infections by pathogenic microorganisms as
Yael Elbaz et al.
The Journal of biological chemistry, 283(18), 12276-12283 (2008-03-07)
Glycine residues may play functional and structural roles in membrane proteins. In this work we studied the role of glycine residues in EmrE, a small multidrug transporter from Escherichia coli. EmrE extrudes various drugs across the plasma membrane in exchange

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