Cetylpyridinium chloride/dyclonine hydrochloride

Analysis Note may contain trace amounts NaCl Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

1,1,2,2-Tetrachloroethane-d 2 is 1,1,2,2-Tetrachloroethane in which all hydrogen atoms are replaced by deuterium. It is commonly employed as an NMR solvent.

1,1,2,2-Tetrachloroethane-d 2 is 1,1,2,2-Tetrachloroethane in which all hydrogen atoms are replaced by deuterium. It is commonly employed as an NMR solvent.

1,1,2,2-Tetrachloroethane-d 2 is 1,1,2,2-Tetrachloroethane in which all hydrogen atoms are replaced by deuterium. It is commonly employed as an NMR solvent.

1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane

1,3-Dichloro-1,1,3,3-tetraisopropyldisiloxane

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

2,3-Dichlorobenzoic acid is an intermediate metabolite of polychlorinated biphenyls (PCBs) .

2,4-Dichloro-6-methylpyrimidine undergoes double cross-coupling reaction with 2-(tributylstannyl)pyridine, followed by aldol condensation to yield 4-arylvinyl-2,6-di(pyridin-2-yl)pyrimidines . It reacts with 1 H ,1 H ,2 H ,2 H -perfluorodecanethiol