225795-35-7 Usage
General Description
2,4,6-tris[[3-(dimethylamino)propylamino]methyl]phenol, also known as TCPP, is a chemical compound commonly used as a flame retardant in various products such as plastics, textiles, and foams. It is a highly efficient flame retardant that works by releasing nitrogen and carbonaceous char when it is heated, thus reducing the flammability of the material. TCPP has been widely used as a flame retardant due to its effectiveness and low cost, although there have been concerns about its potential impact on human health and the environment. Studies have shown that TCPP may have toxic effects on aquatic organisms and could be carcinogenic, leading to increasing scrutiny and debate over its safety and regulation.
Check Digit Verification of cas no
The CAS Registry Mumber 225795-35-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,5,7,9 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 225795-35:
(8*2)+(7*2)+(6*5)+(5*7)+(4*9)+(3*5)+(2*3)+(1*5)=157
157 % 10 = 7
So 225795-35-7 is a valid CAS Registry Number.
225795-35-7Relevant articles and documents
Capillary supercritical fluid chromatography/mass spectrometry of phenolic mannich bases with dimethyl ether modified ethane as the mobile phase
Fuchslueger, Ulf
, p. 2324 - 2333 (1999)
The analysis of phenolic Mannich bases-which are used as hardeners and accelerators for epoxy resins-by capillary supercritical fluid chromatography (SFC) with dimethyl ether modified ethane as the mobile phase is described. The elution properties of several different mobile phases with respect to amines are shown. SFC with UV detection is coupled via a custom-built interface to a mass spectrometer with atmospheric pressure chemical ionization. Two technically important Mannich bases prepared by different production processes are characterized and compared with respect to their byproducts. The role of dimethyl ether during the ionization process and the fragmentation of phenolic Mannich bases is discussed.
