Molecular Biology Reagents

1,1,1-Trifluoroethyl-PEG4-aminooxy is a PEG derivative with trifluoroethyl and aminooxy moieties. The aminooxy group can be used in bioconjugation. It reacts with an aldehyde to form an oxime bond. The hydrophilic PEG linker increases the water

1,1,1-Trifluoroethyl-PEG4-aminooxy is a PEG derivative with trifluoroethyl and aminooxy moieties. The aminooxy group can be used in bioconjugation. It reacts with an aldehyde to form an oxime bond. The hydrophilic PEG linker increases the water

1,1,1-Trifluoroethyl-PEG4-aminooxy is a PEG derivative with trifluoroethyl and aminooxy moieties. The aminooxy group can be used in bioconjugation. It reacts with an aldehyde to form an oxime bond. The hydrophilic PEG linker increases the water

1,1,1-Trifluoropropan-2-amine hydrochloride.

1,1,1-Trifluoropropan-2-amine hydrochloride.

1,1,1-Trifluoropropan-2-amine hydrochloride.

1,1,1-Trifluoropropan-2-amine hydrochloride.

1,1,3,3-Tetramethoxypropane is a precursor of malondialdehyde and a naturally occurring product of lipid peroxidation and prostaglandin biosynthesis, which is formed by oxidation of polyunsaturated fatty acids in foods. It can be mutagenic or

1,1,3,3-Tetramethoxypropane is a precursor of malondialdehyde and a naturally occurring product of lipid peroxidation and prostaglandin biosynthesis, which is formed by oxidation of polyunsaturated fatty acids in foods. It can be mutagenic or

1,1,3,3-Tetramethoxypropane is a precursor of malondialdehyde and a naturally occurring product of lipid peroxidation and prostaglandin biosynthesis, which is formed by oxidation of polyunsaturated fatty acids in foods. It can be mutagenic or

Cyclohexanone dimethyl ketal reacts with trimethylsilane in the presence of trimethylsilyl triflate to form the corresponding ether. It can also undergo allylation and propargylation in the presence of indium to form the corresponding homoallylic or

Cyclohexanone dimethyl ketal reacts with trimethylsilane in the presence of trimethylsilyl triflate to form the corresponding ether. It can also undergo allylation and propargylation in the presence of indium to form the corresponding homoallylic or