推荐产品
形狀
solid
成份
Dye content, 90%
mp
203 °C (dec.) (lit.)
溶解度
95% ethanol: 0.1%
λmax
545 nm
&epsilon ；(消光係數)
≥11000 at 235-241 nm in ethanol: water (1:1) at 0.004%
≥16000 at 286-292 nm in ethanol: water (1:1) at 0.004%
≥78000 at 543-549 nm in ethanol: water (1:1) at 0.004%
應用
diagnostic assay manufacturing
hematology
histology
儲存溫度
room temp
SMILES 字串
CC(O)=O.Nc1ccc(cc1)C(\c2ccc(N)cc2)=C3\C=CC(=N)C=C3
InChI
1S/C19H17N3.C2H4O2/c20-16-7-1-13(2-8-16)19(14-3-9-17(21)10-4-14)15-5-11-18(22)12-6-15;1-2(3)4/h1-12,20H,21-22H2;1H3,(H,3,4)
InChI 密鑰
YIXIVOYGLPFDCY-UHFFFAOYSA-N
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生化／生理作用
Pararosaniline acetate is one of the components of basic fuchsin. It acts as a reversible, linear inhibitor of horse butyrylcholinesterase (BChE).
其他說明
本品为纯净物，是常称作碱性品红的混合物的主要成分。
法律資訊
Magenta is a trademark of Merck KGaA, Darmstadt, Germany
訊號詞
Warning
危險聲明
危險分類
Carc. 2
儲存類別代碼
11 - Combustible Solids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
dust mask type N95 (US), Eyeshields, Gloves
Comparative effects of cationic triarylmethane, phenoxazine and phenothiazine dyes on horse serum butyrylcholinesterase.
Yucel YY
Archives of Biochemistry and Biophysics, 478, 201-205 (2008)
Michael D. Larra?aga, Richard J. Lewis, Robert A. Lewis
Hawley's Condensed Chemical Dictionary (2016)
Tuba Küçükkilinç et al.
Archives of biochemistry and biophysics, 440(2), 118-122 (2005-07-23)
The inhibitory effects of the cationic triarylmethane (TAM+) dyes, pararosaniline (PR+), malachite green (MG+), and methyl green (MeG+) on human plasma cholinesterase (BChE) were studied at 25 degrees C in 100 mM Mops, pH 8.0, with butyrylthiocholine as substrate. PR+
Jingli Xie et al.
Chemical communications (Cambridge, England), (5)(5), 576-578 (2008-01-23)
Salts of the pararosaniline dye cation and four polyoxometalate cluster anions have been isolated under both ambient and hydrothermal conditions; structural and initial spectroscopic data are consistent with significant perturbation of ion electronic states induced by charge-assisted N-H---O hydrogen bonds.
Fernando Maldonado et al.
Journal of colloid and interface science, 351(2), 466-471 (2010-08-28)
Adsolubilisation has been defined as the incorporation to solid-water interfaces of molecules that do not adsorb spontaneously to such interfaces, but can be incorporated through an interaction with an adsorbing surfactant molecule. The aim of this work was to study
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