43141-69-1Relevant articles and documents
Investigation of benzophenoxazine derivatives for the detection of latent fingerprints on porous surfaces
Alsolmy, Eman,Abdelwahab, Walid M.,Martinez, Vincent,Henary, Maged,Patonay, Gabor
, (2020/02/11)
In this report, two classes of benzophenoxazine dyes, Nile red and Nile blue derivatives, were evaluated for the detection of latent fingerprints on porous surfaces. The efficiency to develop fingerprints is influenced by the physical properties of the dye molecules including hydrophobicity as characterized by distribution coefficient value (logD), and other factors such as chemical structure of the dye and hydrogen bonds. Both Nile red and the basic form of Nile blue showed excellent to acceptable ability to detect fingerprints due to their great hydrophobicity at 515 and Crime Scene Search (CSS) settings of the forensic light source. Higher hydrophobicity derivatives of Nile red and Nile blue (in the basic form) improved both quality and sensitivity of fingerprint detection in comparison with their corresponding parent dyes. They developed strong luminescent and visible fingerprints, and a better contrast was achieved between impressions and the background surface suggesting the potential use of these compounds in forensic investigation. Therefore, the hydrophobic derivatives are considered dual-fingerprint reagents because the developed prints can be seen by the naked eye and under illumination process. However, lower hydrophobicity derivatives of Nile red and Nile blue and derivatives with different substituents developed weak or non-luminescent fingerprints with poor contrast. A complete analysis of what dye properties are the most important in fingerprint detection is discussed along with dye optimization for improved performance.
Inter-alkane amidogen phenolic synthetic method (by machine translation)
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, (2019/01/23)
Inter-alkane amidogen phenolic synthetic method, its characteristic is: 1st step, between the two alkane amidogen acyl aniline and sulfuric acid aqueous solution mixing and heating to 50 - 110 °C, thermal insulation reaction of aniline [...] sulfuric acid aqueous solution; 2nd step, continue to drip the sodium nitrite aqueous solution, sodium nitrite aqueous solution for dropping temperature of - 10 - 20 °C, drop bi yu 5 - 30 °C insulation, [...] aniline obtained diazonium salt of the sulfuric acid aqueous solution; 3rd step, [...] aniline diazonium salt of the sulfuric acid aqueous solution is directly heated to 45 - 110 °C, thermal insulation, in the hydrolysis reaction of the diazonium salt, cooling after treatment, to obtain the product between two alkane amidogen phenol; three-step required by the reaction of sulfuric acid in the 1st step reaction in the finished disposable adding; a three-step reaction in a finish step by step in the pot. The method of the invention with raw materials are cheap, abundant, synthetic high security of the process, the product yield is high, the three waste less pollution and the like, has high industrial value. (by machine translation)
Synthetic method for m-dialkylaminophenol
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Paragraph 0020, (2019/01/08)
The invention provides a synthetic method for m-dialkylaminophenol. The synthetic method is characterized by comprising the following steps: step 1, adding an aqueous solution of sodium nitrite into an aqueous solution of sulfuric acid containing m-dialkylaminoaniline drop by drop at a temperature of -10 to 20 DEG C, and maintaining the obtained solution at a temperature of 5 to 30 DEG C for 1 to10 h after completion of the addition so as to obtain an aqueous solution of sulfuric acid containing m-dialkylaminoaniline diazohydrosulfate; and step 2, directly heating aqueous solution of sulfuricacid containing m-dialkylaminoaniline diazohydrosulfate to 45-110 DEG C, maintaining the solution at the temperature for 1-18 h, allowing m-dialkylaminoaniline diazohydrosulfate to undergo the hydrolysis reaction of a diazonium salt, and successively carrying out cooling and post-treatment so as to obtain the product dialkylaminophenol, wherein sulfuric acid needed in the first step and the second step is totally added in one shot in a first-step reaction, and the first-step diazotization reaction and the second-step hydrolysis reaction of the diazonium salt are carried out step by step in one pot. The method of the invention has the characteristics of low raw material price, sufficient raw material sources, high safety, high product yield, less three-wastes pollution and the like, and has high industrialization value.