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62825-32-5

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62825-32-5 Usage

Description

Bromocresol Green Sodium Salt is a synthetic dye that possesses the ability to act as a pH indicator. It is characterized by its yellow color in acidic environments and blue color in alkaline conditions, making it a useful tool for various applications in different industries.

Uses

Used in Analytical Chemistry:
Bromocresol Green Sodium Salt is used as a pH indicator for monitoring and measuring pH changes in different solutions. Its color change from yellow to blue as the pH increases makes it a reliable and visually distinct indicator for various analytical purposes.
Used in Microplate Reader Studies:
In the field of yeast physiological research, Bromocresol Green Sodium Salt is employed as a pH indicator in microplate readers. It aids in the study of yeast growth curves and the monitoring of pH changes in the medium, providing valuable insights into the yeast's metabolic activities and environmental adaptations.
Used in Dual Indicator Systems:
Bromocresol Green Sodium Salt can be combined with another pH indicator to create a dual indicator system. This system allows for more accurate and precise measurement of pH changes in a medium, as the two indicators can cover a broader pH range and provide a more detailed understanding of the environmental conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 62825-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,2 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 62825-32:
(7*6)+(6*2)+(5*8)+(4*2)+(3*5)+(2*3)+(1*2)=125
125 % 10 = 5
So 62825-32-5 is a valid CAS Registry Number.

62825-32-5Downstream Products

62825-32-5Relevant articles and documents

Infrared spectra of several thiopiperidides and thiomorpholides

Cornea, Felicia,Cercasov, Cornelia,Ciureanu, Mariana

, p. 775 - 782 (2007/10/02)

Infrared spectra in the 1700-500 cm-1 region have been studied for several types of thiopiperidides (thiobenzoylpiperidides, thiocinnamoylpiperidides and phenylthioacetpiperidides) and for the corresponding thiomorpholides.Three characteristic thioamide bands were located and assigned.The behaviour of these bands on molecular complexing (with iodine as an electron acceptor) was used to support the assignments.The experimental data were discussed in terms of the theoretical results obtained by an HMO procedure.

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