Di-tert-butyl dicarbonate is an organic synthesis, and its use is very wide, it can have a very special role in the protection of amino acids, so it is very widely used in medicine, for protein, peptide synthesis and biological chemical food, and cosmetics, etc.. This substance also has a lot of advantages, so the following is About this issue, let's learn together.
First of all, its price is very cheap, so if you use it as synthesis, you can reduce a lot of costs, besides, there is no strong and irritating taste, and it is not toxic to our body, but after contacting with skin, it may lead to skin allergy, so you need to wash it with water in time. There is also the peptide synthesis in this product, also pay attention to the protection of the gene removal, mild conditions, so as to be more purified, for the amino acid protection effect is also better.
Di-tert-butyl dicarbonate is a kind of organic synthesis in medicine, intermediate can be used in the synthesis of pharmaceutical and agrochemical products, but also as a protective agent for amino acids. It has a very important role in our daily application, and its safety is relatively high, there is no obvious harm to our body, but we should pay attention to the standard operation and storage away from heat sources.
Uses of the product.
1、Pharmaceutical and organic synthesis intermediates, is an important application in the synthesis of pharmaceutical and agrochemical products amino protective agent
2、Used as intermediates of pharmaceutical and organic synthesis, it is an important amino protective agent used in the synthesis of pharmaceutical and agrochemical products.
3、In organic chemistry reaction, it is often used as tert-butoxycarbonylation reagent for amine, phenol, thiol, amide, lactam, carbamate and other substrates, the reaction rate is fast and the yield is relatively high. tert-butoxycarbonylation reaction (protection of functional groups). Because of the poor stability of acyl halide reagents, they are widely used as the protecting group of amino groups, which can be removed under acidic conditions (e.g., hydrochloric acid, trifluoroacetic acid, etc.). Aliphatic amines, alicyclic amines, aromatic amines and heterocyclic amines are able to react with (Boc).
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