Nitro

<p>Applications N,N-dimethyl-2,4-dinitroaniline (cas# 1670-17-3) is a useful research chemical.<br></p>

<p>Applications Toxic to some wild and domestic birds and mice. Molluscicidal activity<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References De Abreu, F. et al.; Bioorg. Med. Chem. 9, 659 (2001); Schafer, E.W. et al.; Arch. Environ. Con. Tox. 14, 111 (1985); Schafer, E.W. et al.; Arch. Environ. Con. Tox. 12, 355 (1983)<br></p>

<p>Applications 4-hydroxy-2-nitrobenzoic acid (cas# 74230-08-3) is a useful research chemical.<br></p>

<p>Applications Methyl 3-nitroisonicotinate (cas# 103698-10-8) is a useful research chemical.<br></p>

<p>Applications 2-(2-Nitroanilino)ethanol is used in the preparation of (phenylamino)quinoxalinone derivatives which has been identified as a new class of glycogen phosphorylase inhibitors.<br>References Dudash, J., et al.: Bioorg. Med. Chem. Lett., 21, 4790 (2005); Hellerstein, M., et al.: J. Clin. Invest. 100, 1305 (1994)<br></p>

<p>Stability Hygroscopic<br>Applications 4-Nitrobenzoic Acid is used in the synthesis of anti-Trypanosoma cruzi agents in the treatment of chagas disease.<br>References Palace-Berl, F. et al.: Bioorg, Med. Chem. Lett., 21, 5395 (2013); Zhou, L. et al.: J. Med. Chem., 56, 796 (2013);<br></p>

<p>Applications 3-Nitrobenzoylacetonitrile (cas# 21667-64-1) is a useful research chemical.<br></p>

<p>Applications N,N-Diamylnitrosamine (cas# 13256-06-9) is a compound useful in organic synthesis.<br></p>

<p>Stability Stable at RT<br>Applications An intermediate used for the sythesis of xanthine derivatives.<br>References Daly, J.W., et al.: J. Med. Chem., 28, 487 (1985), Erickson, R.H., et al.: J. Med. Chem., 34, 3405 (1991),<br></p>

<p>Applications N-Ethyl-N-(2-hydroxyethyl)nitrosamine is a member of the nitrosamine class of carcinogens and induces renal cancer. It has been shown to induce tumors in the kidneys of rats and in the lungs of mice.<br>References Hiasa, Y., et al.: Cancer Lett, 145, 143-149 (1999)<br></p>

<p>Applications 4-Nitrocatechol can be used as a catalyst and an antibacterial against intestinal bacteria.<br>References Jones, Matthew D., et al.: Polymer Preprints (Amer. Chem. Soc.), 48(2), 873-874 (2007);Jeong, Eun-Young, et al.: Food Chem.,  115(3), 1006-1010 (2009)<br></p>

<p>Applications 3,4-Dinitroaniline is a useful intermediate for the preparation of various industrially important chemicals like dyes, pestices, herbicides and other useful research chemicals.<br>References Sivakumar, K. K., et al.: Int. J. Res. Pharm. Chem., 4, 517 (2014); Shahinian, E. G. H., et al.: Sci. Bull. B: Chem. Mater. Sci., 73, 153 (2011); Jahn, U.: Science of Synthesis, 41, 371 (2010)<br></p>

<p>Applications N,N-Diethyl-4-nitroaniline<br></p>

<p>Stability Hygroscopic<br>Applications N-(3-Hydroxypropyl) 4-hydroxy-2-nitroaniline is a hair ingredient. It is used as a semipermanent (nonoxidative) hair colorant and as a toner in permanent (oxidative) hair dye products.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Burnett, C. L., et al.: Int. J. Toxicol., 28, 217S (2009); Yazar, K., et al.: Contact Dermatitis, 61, 269 (2009)<br></p>

<p>Applications 2-nitrobenzene-1,4-diamine (cas# 5307-14-2) is a useful research chemical.<br></p>

<p>Applications ETHYL 4-NITROBENZOATE (cas# 99-77-4) is a useful research chemical.<br></p>

<p>2-Amino-5-nitro-2'-chlorobenzophenone (2ACCB) is a precursor for the synthesis of 2,4,6-trichlorophenol. 2ACCB reacts with hydrochloric acid in the presence of a scrubber to produce diphenyl ether and activated 2ACCB. The reaction rate can be increased by adding sodium hydroxide solution to the reaction solution. The hydroxy group on the 2ACCB molecule can be converted to a terpene by transfer reactions with glycol esters. This compound has been used as a sterilant and disinfectant in reaction solutions containing chlorine atoms or carbonyl groups.</p>

<p>2,5-Dichloronitrobenzene is a compound that is used to manufacture dyes and pharmaceuticals. It can be synthesized from sodium carbonate, 4-tert-butylbenzoic acid, and sodium hydroxide solution. To produce 2,5-dichloronitrobenzene, the reactants are heated in a reaction vessel with a diphenyl ether as an acid catalyst. The product of this reaction is then dissolved in deionized water or water containing other solvents such as methanol or ethanol. The reaction yield is approximately 95%. The byproducts of this process include 2-chloroacetophenone and hydrogen chloride gas. 2,5-Dichloronitrobenzene reacts with sodium hydroxide solution to form 4-tert-butyl benzoic acid and sodium chloride. This reaction occurs because these compounds have polar functional groups which can form hydrogen bonds with each</p>

<p>6-Chloro-2-nitrotoluene is a synthetic organic compound that has been identified in environmental samples as a reaction product of chlorine and organic compounds. It has been shown to induce root formation in plants, which is related to its ability to inhibit the formation of chlorinated hydrocarbons. 6-Chloro-2-nitrotoluene can be produced by reacting nitrogen atoms with zirconium at high temperatures and low pressures, requiring an activation energy of 50 kcal/mol.</p>