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Acid Red 51, also known as New Coccine, is a synthetic azo dye characterized by its red to orange powder form. It is widely recognized for its use in coloring various products across different industries, despite potential health concerns related to skin and eye irritation, allergic reactions, and possible carcinogenic properties.

568-63-8

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568-63-8 Usage

Uses

Used in Food Industry:
Acid Red 51 is used as a coloring agent for enhancing the visual appeal of food products such as jams, jellies, and baked goods. Its vibrant red hue contributes to the aesthetic quality of these items, making them more attractive to consumers.
Used in Textile Industry:
In the textile industry, Acid Red 51 serves as a dyeing agent for coloring various fabrics and materials. Its ability to impart a rich red color makes it a popular choice for manufacturers looking to create visually striking textiles.
However, due to the potential health risks associated with Acid Red 51, strict regulations and limits on its use have been established across industries to ensure consumer safety and minimize exposure to these risks.

Check Digit Verification of cas no

The CAS Registry Mumber 568-63-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,6 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 568-63:
(5*5)+(4*6)+(3*8)+(2*6)+(1*3)=88
88 % 10 = 8
So 568-63-8 is a valid CAS Registry Number.
InChI:InChI=1/C20H8I4O5.2Na/c21-11-5-9-13(7-3-1-2-4-8(7)20(27)28)10-6-12(22)17(26)15(24)19(10)29-18(9)14(23)16(11)25;;/h1-6,25H,(H,27,28);;/q;2*+1/p-2

568-63-8 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (A14180)  Erythrosin B   

  • 568-63-8

  • 25g

  • 334.0CNY

  • Detail
  • Alfa Aesar

  • (A14180)  Erythrosin B   

  • 568-63-8

  • 100g

  • 1155.0CNY

  • Detail
  • Alfa Aesar

  • (A14180)  Erythrosin B   

  • 568-63-8

  • 500g

  • 3980.0CNY

  • Detail

568-63-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Acid Red 51

1.2 Other means of identification

Product number -
Other names EOSIN IODO

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:568-63-8 SDS

568-63-8Synthetic route

silver (I) ion
14701-21-4

silver (I) ion

erythrosin
568-63-8

erythrosin

2Ag(1+)*C20H6I4O5(2-)=Ag2C20H6I4O5

2Ag(1+)*C20H6I4O5(2-)=Ag2C20H6I4O5

Conditions
ConditionsYield
In water 25°C, constant ionic strength (KNO3), various concns. of dye; no isolation, identification by potentiometric titration of dye soln. by AgNO3;
erythrosin
568-63-8

erythrosin

silver nitrate

silver nitrate

2Ag(1+)*C20H6I4O5(2-)=Ag2C20H6I4O5

2Ag(1+)*C20H6I4O5(2-)=Ag2C20H6I4O5

Conditions
ConditionsYield
In water excess of AgNO3; ppt. washed, dried;

568-63-8Upstream product

568-63-8Downstream Products

568-63-8Relevant academic research and scientific papers

A Nanosecond Laser Flash Photolysis Study of Intramicellar Reactions in the Erythrosin B/CTAB Aqueous System

Flamigni, Lucia

, p. 3331 - 3337 (2007/10/02)

Both "fast", occurring within 1 μs after excitation, and "slow" reactions, occurring in the hundreds of microseconds time scale, were observed following erythrosin B triplet formation in the cationic micellar system cetyltrimethylammonium bromide (CTAB).The "fast" events are shown to occur in multiply occupied micelles and are assigned to bimolecular reactions.The "slow" ones, which have not been studied in detail, are due to first-order deactivation processes of the triplet occurring in singly occupied micelles.The effects of the excitation intensity and occupancy on the fast triplet decay, radical formation, and subsequent geminate recombination have been studied.The triplet disappears with observed rate constants ranging from 5.5 * 1E6 to 3.6 * 1E6 s-1 while the formation of radicals has rate constants varying from 3.3 * 1E7 to 9.1 * 1E6 s-1.Both in triplet decay and in radical formation the increase in rates occurs by increasing the excitation energy and occupancy.The identification of the precursor(s) of radicals is discussed.The geminal radical recombination has a rate constant of 2.1 * 1E6 s-1.

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