(S,S)-(-)-Bis(α-methylbenzyl)amine Hydrochloride CAS# 40648-92-8

(S,S)-(-)-Bis(α-methylbenzyl)amine Hydrochloride , Promotion Season Now in Store and Free Sample for Testing with Factory Price

Chemical Name: (S,S)-(-)-Bis(α-methylbenzyl)amine Hydrochloride
CAS No.: 40648-92-8
Molecular Fomula: C16H20ClN
Molecular weight:261.79
Appearance: White Low Melting Crystalline Solid
Sample: Available

(S,S)-(-)-Bis(α-methylbenzyl)amine Hydrochloride CAS# 40648-92-8

Description of DBDC

Boc anhydride is a flammable liquid. Melting point 23°C, boiling point 56-57°C (6.55E-2kPa). It is used in organic synthesis to introduce tert-butoxycarbonyl protecting groups.

Basic Info of DBDC

Chemical Name






Molecular Formula


Molecular Weight






Safety Info

Safety Statements

S26; S36; S36/37/39

HS Code


Risk Statements

R36/37/38; R22

Hazard Codes

Xi; Xn


Boiling Point

296.5ºC at 760 mmHg

Melting Point


Flash Point


Numbering system

MDL number


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What is DBDC?

With the progress of science and technology and the development of society, chemical products have invariably permeated our daily lives, in medicine, food, cosmetics, electronics, industry, and other areas, becoming an essential part of our lives. One such product is (S,S)-(-)-Bis(α-methylbenzyl)amine Hydrochloride which has developed particularly rapidly in recent years. Do you know about (S,S)-(-)-Bis(α-methylbenzyl)amine Hydrochloride?

The official answer:Di-tert-butyl dicarbonate (Boc acid anhydride) is used in organic synthesis to introduce tert-butoxycarbonyl protection genes, especially for the amino protection of amino acids. It is widely used in the synthesis of pharmaceuticals, protein and peptide synthesis, biochemical foods, cosmetics and many other products.Used as an intermediate in pharmaceutical and organic synthesis, it is an important aminoprotectant used in the synthesis of pharmaceutical and agrochemical products.

What’s the application of (S,S)-(-)-Bis(α-methylbenzyl)amine Hydrochloride?

Amino acid BOC reagent. Used in organic synthesis to introduce tert-butoxycarbonyl (BOC) protecting groups, particularly suitable for amino acid protection of amino acids. Tri-Boc-protected hydrazines can be used in colouring reagents to prepare fluorenylmethoxycarbonyl esters to monitor solid phase aldehydes. Reagents for the preparation of tert-butoxycarbonyl-protected amines. Reagents for the introduction of tert-butoxycarbonyl-protected moieties. Alcohols such as tert-butoxycarbonyl derivatives can be protected by Lewis acid catalysis. Preparation of aminomethyl propadiene by the reaction of tert-butoxycarbonylaminopropyne with formaldehyde, diisopropylamine and copper bromide, a component of many bovine plasma amine oxidase inactivators.


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