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Thionine (acetate), also known as acetate thionine or 2,8-diamino-5-[(2-hydroxyethyl)amino]-4-[(2-hydroxyethyl)amino]phenazine-3,7-diol diacetate, is a chemical compound derived from the parent compound thionine, a phenothiazine dye. It is a blue-colored substance with the molecular formula C22H26N6O6S2 and a molecular weight of 534.61 g/mol. Thionine acetate is used as a redox indicator in titrations, particularly in the determination of iron(II) ions, where it changes color from blue to colorless upon reduction. It is also employed in various analytical applications and as a stain in histology and microbiology. The compound is soluble in water and ethanol, and its chemical properties make it useful in a range of scientific and industrial processes.

635-76-7

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635-76-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 635-76-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,3 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 635-76:
(5*6)+(4*3)+(3*5)+(2*7)+(1*6)=77
77 % 10 = 7
So 635-76-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H9N3S.ClH/c13-7-1-3-9-11(5-7)16-12-6-8(14)2-4-10(12)15-9;/h1-6,13H,14H2;1H/b13-7+;

635-76-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name thionine cloride

1.2 Other means of identification

Product number -
Other names hydrochloride

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:635-76-7 SDS

635-76-7Relevant academic research and scientific papers

Kinetic study on the reversible hydride transfer between methylene blue and thionine

Liu,Yamamoto,Fujiyama,Sueishi

, p. 2367 - 2371 (2007/10/03)

The kinetics of the hydride transfer reaction between leuco methylene blue and thionine was investigated spectrophotometrically by means of the stopped-flow technique. Leuco methylene blue and leuco thionine were produced by photoreduction of methylene bl

PHOTOREDUCTION OF THIONINE AND SURFACTANT THIONINE BY IRON(II) IN ANIONIC MICELLES AND MICROEMULSIONS.

Mackay,Graetzel

, p. 526 - 530 (2007/10/02)

The rate constants for the iron(II)-thionine and surfactant thionine system have been determined in aqueous solution, sodium dodecyl sulfate (SDS) micelles, and in a mineral oil-in-water microemulsion stabilized by sodium cetyl sulfate (SCS) and 1-pentanol. The triplet lifetimes are all in the range 7-9 mu s. The rate constant for electron transfer quenching of triplet thionine by iron(II) is higher in the anionic media due to a higher local Fe**2** plus concentration. However, the back reaction between semithionine and iron(III) is not similarly enhanced in the presence of micelles or microemulsion. The dismutation of semithionine is a little slower in microemulsion than in water, but over two orders of magnitude slower in SDS micelles. The quantum yield of thionine triplet formation, determined for surfactant thionine in SCS microemulsion, approaches unity.

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