Svoboda | Graniru | BBC Russia | Golosameriki | Facebook

To install click the Add extension button. That's it.

The source code for the WIKI 2 extension is being checked by specialists of the Mozilla Foundation, Google, and Apple. You could also do it yourself at any point in time.

How to transfigure the Wikipedia

Would you like Wikipedia to always look as professional and up-to-date? We have created a browser extension. It will enhance any encyclopedic page you visit with the magic of the WIKI 2 technology.

Try it — you can delete it anytime.

Install in 5 seconds
4,5
Kelly Slayton
Congratulations on this excellent venture… what a great idea!
Alexander Grigorievskiy
I use WIKI 2 every day and almost forgot how the original Wikipedia looks like.
Live Statistics
English Articles
Improved in 24 Hours
Added in 24 Hours
What we do. Every page goes through several hundred of perfecting techniques; in live mode. Quite the same Wikipedia. Just better.
Great Wikipedia has got greater.
.
Leo
Newton
Brights
Milds

Xylenol orange

From Wikipedia, the free encyclopedia

Xylenol orange
Names
Preferred IUPAC name
2,2′,2′′,2′′′-{(1,1-Dioxo-2,1λ6-benzoxathiole-3,3(1H)-diyl)bis[(6-hydroxy-5-methyl-3,1-phenylene)methylenenitrilo]}tetraacetic acid
Other names
XO[1]
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.015.049 Edit this at Wikidata
EC Number
  • 216-553-8
UNII
  • InChI=1S/C31H32N2O13S/c1-17-7-21(9-19(29(17)42)11-32(13-25(34)35)14-26(36)37)31(23-5-3-4-6-24(23)47(44,45)46-31)22-8-18(2)30(43)20(10-22)12-33(15-27(38)39)16-28(40)41/h3-10,42-43H,11-16H2,1-2H3,(H,34,35)(H,36,37)(H,38,39)(H,40,41) checkY
    Key: ORZHVTYKPFFVMG-UHFFFAOYSA-N checkY
  • O=C(O)CN(CC(=O)O)Cc1c(O)c(cc(c1)C3(OS(=O)(=O)c2ccccc23)c4cc(c(O)c(c4)CN(CC(=O)O)CC(=O)O)C)C
Properties
C31H32N2O13S
Molar mass 672.66 g·mol−1
Melting point 195 °C (383 °F; 468 K)
200 mg/mL
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H315, H319, H335
P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 1: Must be pre-heated before ignition can occur. Flash point over 93 °C (200 °F). E.g. canola oilInstability 2: Undergoes violent chemical change at elevated temperatures and pressures, reacts violently with water, or may form explosive mixtures with water. E.g. white phosphorusSpecial hazards (white): no code
2
1
2
Flash point > 93 °C (199 °F; 366 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Xylenol orange is an organic reagent, most commonly used as a tetrasodium salt as an indicator for metal titrations. When used for metal titrations, it will appear red in the titrand and become yellow once it reaches its endpoint. Historically, commercial preparations of it have been notoriously impure,[2] sometimes consisting of as little as 20% xylenol orange, and containing large amounts of semi-xylenol orange and iminodiacetic acid. Purities as high as 90% are now available.

It is fluorescent, and has excitation maximums of 440 & 570 nm and an emission maximum of 610 nm.[3]

YouTube Encyclopedic

  • 1/3
    Views:
    2 696
    637
    577
  • Lipid Peroxidation || Measurement of Free Radical Burden
  • To estimate strength of Cu and Zn in the given mixture
  • Quality Control - Prof. Ahmed Habib - lecture 8 for Fourth year / 9 for fourth level clinical

Transcription

References

  1. ^ Li, Zhong-Guang (2019-01-01), Khan, M. Iqbal R.; Reddy, Palakolanu Sudhakar; Ferrante, Antonio; Khan, Nafees A. (eds.), "Chapter 5 - Measurement of Signaling Molecules Calcium Ion, Reactive Sulfur Species, Reactive Carbonyl Species, Reactive Nitrogen Species, and Reactive Oxygen Species in Plants", Plant Signaling Molecules, Woodhead Publishing, pp. 83–103, ISBN 978-0-12-816451-8, archived from the original on 2023-11-11, retrieved 2023-11-11
  2. ^ Gay, Craig; Collins, James; Gebicki, Janusz M. (1999), "Determination of Iron in Solutions with the Ferric–Xylenol Orange Complex", Analytical Biochemistry, 273 (2): 143–148, doi:10.1006/abio.1999.4207, PMID 10469483
  3. ^ "Fluorescence - Fluorochrome Data Tables". Molecular Expressions Microscopy Primer: Specialized Microscopy Techniques. 2018-09-11. Retrieved 2020-01-30.


Stub icon

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

This page was last edited on 19 February 2024, at 17:37
Basis of this page is in Wikipedia. Text is available under the CC BY-SA 3.0 Unported License. Non-text media are available under their specified licenses. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc. WIKI 2 is an independent company and has no affiliation with Wikimedia Foundation.
Contact WIKI 2
Introduction
Terms of Service
Privacy Policy