2150-58-5 Usage
Description
PHENOL BLUE is an organic dye compound characterized by its dark brown to black fine crystalline powder form. It is known for its chemical properties and potential applications in various industries.
Uses
Used in Dye Industry:
PHENOL BLUE is used as a coloring agent for its ability to impart color to various materials. Its dark brown to black hue makes it suitable for a range of applications within the dye industry.
Used in Metabolic Studies:
In the field of biochemistry and medical research, PHENOL BLUE serves as an indicator in metabolic studies. It is utilized to track and visualize metabolic processes due to its ability to change color in response to different chemical environments.
Used in Analytical Chemistry:
PHENOL BLUE is employed as a pH indicator in analytical chemistry. Its color-changing properties allow it to be used in titrations and other chemical analyses where pH measurement is crucial.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, PHENOL BLUE is used as an additive in the formulation of certain medications. Its properties may contribute to the stability, appearance, or other characteristics of the final product.
Please note that the provided materials do not specify the exact applications of PHENOL BLUE. The uses listed above are inferred based on the general properties of similar organic dye compounds and their typical applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 2150-58-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,5 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2150-58:
(6*2)+(5*1)+(4*5)+(3*0)+(2*5)+(1*8)=55
55 % 10 = 5
So 2150-58-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H14N2O/c1-16(2)13-7-3-11(4-8-13)15-12-5-9-14(17)10-6-12/h3-10H,1-2H3
2150-58-5Relevant articles and documents
Electrochemical synthesis and mechanestic study of quinone imines exploiting the dual character of N,N-dialkyl-p-phenylenediamines
Maleki, Abbas,Nematollahi, Davood
supporting information; experimental part, p. 1928 - 1931 (2011/06/21)
Two one-pot electrochemical approaches for the synthesis of similar quinone imines via either the nucleophilic character of N,N-dialkyl-pphenylenediamines or electrophilic reactivity of their oxidized forms through Michael-type addition reactions are reported.