Nitro

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

<p>Applications rac-4-Benzyloxy-3-nitrostyrene Oxide (cas# 51582-41-3) is a compound useful in organic synthesis.<br>References Karellas, P., et al.: J. Med. Chem., 51, 6128 (2008),<br></p>

<p>Applications 1,5-Dinitroanthraquinone 97% (cas# 82-35-9) is a useful research chemical.<br></p>

<p>Applications Nitrofurate is a useful organic reagent. It is used for preparation of polycyclic small molecules.<br>References Tan, D., et al.: J. Am. Chem. Soc., 121, 9073 (1999); Lu, P., et al.: Org. Lett., 11, 5710 (2009);<br></p>

<p>Applications 3,5-DINITRO-4-HYDROXYBENZOIC ACID (cas# 1019-52-9) is a useful research chemical.<br></p>

<p>Applications Nitrobenzene is a compound that exhibits chromosomal genotoxicity against hamster lung cells, and has the potential to cause cancer in humans (1,2). Nitrobenzene is also used as a starting material to synthesize 4-Aminophenol (A618920) through catalytic hydrogenation (3). Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants.<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 1. Bonacker, D. et al.: Arch. Toxicol. 2004 Jan;78(1):49-57.2. Hsu, C. et al.: J. Environ. Sci. Health. C. Environ. Carcinog. Ecotoxicol. Rev. 2007 Apr-Jun;25(2):155-843. Rode, C. et al.: Org. Proc. Res. Dev. 1999 Nov;3(6), pp 465–470<br></p>

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

<p>Impurity Albendazole Impurity 4<br>Applications 2-Nitroaniline, is the main precursor to phenylenediamines, which are converted to benzimidazoles, a family of heterocycles that are key components in pharmaceuticals. Albendazole Impurity 4<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 Booth, G.,et al.: Ull. Encyc. Indust. Chem. (2007);<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 N,N-Diamylnitrosamine (cas# 13256-06-9) is a compound useful in organic synthesis.<br></p>

<p>Applications 4-Amino-1,3-dimethyl-5-nitrosouracil is a useful building block for organic synthesis.<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>Applications Ethyl Nitroacetate is an ester of nitrocarboxylic acid used as an intermediate in the preparation of unsubstituted amino acids.<br>References Sidorin, G.I.: Gig. Aspe. Okhr. Zdor. Nasel., 144 (1977);<br></p>

<p>Applications 1,3-Dinitrobenzene is used as an analyte to detect explosive environments (1), including those containing picric acid (2). Neurotoxic agent (3). Drinking water contaminant candidate (CCL3) as per United States Environmental Protection Agency (EPA). Environmental contaminants; Food contaminants.<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 1. ÄŒapka, L. et al.: J. Chromatogr. A. 2015 Apr 3;1388:167-73.2. Sanda, S. et al.: Chem. Commun. (Camb) 2015 Apr 18;51(30):6576-93. Maurer, L. et al.: Neurotoxicology. 2016 Mar;53:74-84<br></p>

<p>Applications N-(Nitrosomethyl)ethanolamine can be used to study the chemical-molecular perspective of the liver specificity of the carcinogenicity of NOCs.<br>References Yuan, J., et.al.: Chem. Res. Toxicol., 25, 2432-2442, (2012);<br></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.

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

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.