6627-48-1 Usage
Uses
Used in Pharmaceutical Industry:
2,4,6-trinitrophenol 2-aminoethanol (1:1) is used as an intermediate in the synthesis of certain pharmaceutical compounds for its potential to enhance the properties of drugs, leveraging the reactivity and functional groups of both components.
Used in Explosives Industry:
In the explosives industry, 2,4,6-trinitrophenol 2-aminoethanol (1:1) is used to improve the performance characteristics of explosive formulations, capitalizing on the explosive properties of picric acid and the solvent properties of 2-aminoethanol to create more effective blasting agents.
Used in Dyes and Pigments Industry:
2,4,6-trinitrophenol 2-aminoethanol (1:1) is utilized as a component in the production of dyes and pigments, taking advantage of the color-producing capabilities of picric acid and the ability of 2-aminoethanol to act as a solvent or modifier for these compounds.
Used in Insecticides Industry:
Within the insecticides industry, 2,4,6-trinitrophenol 2-aminoethanol (1:1) is employed to enhance the effectiveness of insecticidal products, using the toxic properties of picric acid in combination with the solvent properties of 2-aminoethanol to improve the delivery and action of the insecticide.
Check Digit Verification of cas no
The CAS Registry Mumber 6627-48-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,2 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6627-48:
(6*6)+(5*6)+(4*2)+(3*7)+(2*4)+(1*8)=111
111 % 10 = 1
So 6627-48-1 is a valid CAS Registry Number.
6627-48-1Relevant academic research and scientific papers
Poonia, Narinder S.,Chandra, Ramesh,Sheldrick, W. S.
, p. 1512 - 1514 (1990)
2-Hydroxyethanaminium picrate, HOCH2CH2NH3+*C6H2N3O7-, is prepared through a metathetical reaction of Mg(Pic)2 and HOCH2CH2NH2 (2-aminoethanol, MEA) in ethanol through in situ generation of HPic.Orange yellow crystals (MEAH+Pic-) (mp 163 deg C) of the "Salt" are produced along with the colorless Mg(CH2NH2CH2O-)2, even when MEA is less than 1:1 with respect to Mg(Pic)2.The crystals are monoclinic, space group P21/c, a=11.797(4), b=14.288(3), c=7.124(2) Angstroem, β=97.63(2) deg, Z=4.Dcal=1.62 g cm-3.Structural analysis from the 1617 reflection data (R=0.059, Rw=0.056) reveals that the picric acid proton is formally transferred to the MEA nitrogen (N-H, 0.968 Angstroem) and is merely bonded to the phenoxide of Pic(H...O-, 1.951 Angstroem) and weakly also to an oxygen of o-nitro group of the anion (H...ONO, 2.379 Angstroem).The transferred proton becomes and integral part of the cation MEAH+ and completes the fourth covalent bond of the sp3 N of MEA, and does not show any special affinity for the anionic oxygen of Pic; the N-H...O- (142.8 deg) and N-H...ONO (141.6 deg) angles are closely comparable.
