Isoniazid

1-Adamantyl isocyanate is an isocyanate derivative. Application 1-Adamantyl isocyanate may be used in the preparation of: adamantyl-functionalized nanoparticles, via thiol-isocyanate reaction of thiol-modified nanoparticles1 4-[3-(aryl or

Application 2&#8242,3&#8242-O-Isopropylideneguanosine derivatives may be used as cap analogs.

Application 2&#8242,3&#8242-O-Isopropylideneguanosine derivatives may be used as cap analogs.

2-Ethylhexyl isocyanate

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-Isopropylmalic acid is an intermediate formed during leucine biosynthesis. Budding yeast Saccharomyces cerevisiae secrets 2-isopropylmalic acid and helps in reduction of aluminum toxicity by forming chelate with Al ions, thereby preventing them

2-ISOPROPYLMALIC ACID

3-Methoxybenzyl isocyanate (3MBITC) is the degradation product of glucolimnanthin, a glucosinolate found in meadowfoam (Limnanthes alba) seed oil. Application 3-Methoxybenzyl isocyanate may be used to synthesize the following thiourea derivatives:

Benthiavalicarb isopropyl is classified under the class of amino acid amide carbamate category of fungicides. Application Benthiavalicarb isopropyl may be used as an analytical reference standard for the determination of benthiavalicarb isopropyl

Ethyl isocyanate undergoes trimerization at high temperature for the synthesis of Isocyanurates. Application Ethyl isocyanate may be used to generate thermoresponsiveness in polyglycidol via partial hydrophobic modification.

Ethyl isocyanate undergoes trimerization at high temperature for the synthesis of Isocyanurates. Application Ethyl isocyanate may be used to generate thermoresponsiveness in polyglycidol via partial hydrophobic modification.