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C.I. 482200, also known as Basic Red 14, is a synthetic organic dye that belongs to the class of cationic dyes. It is characterized by its bright red color and good light fastness properties, making it a popular choice for dyeing natural fibers such as cotton and wool. However, due to its synthetic nature, it may pose environmental and health risks if not handled and disposed of properly, necessitating cautious use and adherence to regulations.

38775-22-3

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38775-22-3 Usage

Uses

Used in Textile Industry:
C.I. 482200 is used as a dyeing agent for natural fibers such as cotton and wool due to its bright red color and good light fastness properties. It provides a vibrant and long-lasting color to textiles, making it a popular choice for various textile products.
Used in Paper Industry:
In the paper industry, C.I. 482200 is used as a coloring agent to impart a bright red hue to paper products. Its good light fastness ensures that the color remains vibrant and resistant to fading over time, enhancing the visual appeal of paper products.

Check Digit Verification of cas no

The CAS Registry Mumber 38775-22-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,7 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 38775-22:
(7*3)+(6*8)+(5*7)+(4*7)+(3*5)+(2*2)+(1*2)=153
153 % 10 = 3
So 38775-22-3 is a valid CAS Registry Number.

38775-22-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (E,E)-4,4'-bis[2-sulfostyryl]biphenyl

1.2 Other means of identification

Product number -
Other names Einecs 254-121-0

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:38775-22-3 SDS

38775-22-3Upstream product

38775-22-3Relevant academic research and scientific papers

Strong Intermolecular Electronic Coupling of Chromophores Confined in Hydrogen-Bonded Frameworks

Adachi, Takuji,Connors, David M.,Xiao, Wenchang,Hu, Chunhua,Ward, Michael D.

, p. 3366 - 3373 (2015)

Guanidinium organodisulfonate (GDS) hydrogen-bonded frameworks constructed from "tetris-shaped" ortho-substituted disulfonated stilbene derivatives display crystal architectures in which the stilbenes serve as pillars that connect opposing guanidinium sulfonate (GS) sheets in a continuously layered architecture while guiding the organization of the stilbene residues into packing motifs that produce unique optical properties. The constraints imposed by ortho-substitution result in a heretofore unreported topology of the pillars projecting from the two-dimensional GS sheet, while the dense packing of stilbene constituents, confined between the GS sheets, results in strong intermolecular electronic coupling. Stilbene 420 (2,2″-([1,1′-biphenyl]-4,4′-diyldi-2,1-ethenediyl)bis-benzenesulfonate) pillars pack in a face-to-face brickwork motif, producing a large bathochromic shift (~100 nm) of the absorbance and emission spectra relative to stilbene 420 in methanol. The distyrylbenzenedisufonate (2,2′-((1E,1′E)-1,4-phenylenebis(ethene-2,1-diyl))dibenzenesulfonate) pillars, which pack in a face-to-face herringbone motif between the GS sheets, afford both hypsochromic and bathochromic shifts in their absorption spectrum, indicative of an unusually large Davydov splitting. The observation of both bathochromic and hypsochromic shifts can be attributed to the herringbone arrangement, in which both transitions are allowed due to the nonzero vector sum of the transition dipoles in both states. The large magnitude of the Davydov splitting reflects the strong intermolecular coupling between the chromophores, enforced by confinement in the GS framework. The newly discovered GS architectures evoke a new design rule that permits prediction of GS topologies in the case of longer tetris-shaped pillars. (Chemical Equation Presented).

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