tert-Butyl (4-aMinobutyl)carbaMate hydrochloride

tert-Butyl (4-aMinobutyl)carbaMate hydrochloride - Names and Identifiers

Name	4-[(tert-butoxycarbonyl)amino]butan-1-aminium chloride
Synonyms	BOC-DAB HCL N-Boc-putrescine BOC-1,4-DIAMINOBUTANE HCL N-BOC-1,4-DIAMINOBUTANE-HCl BOC-1,4-DIAMINOBUTANE HYDROCHLORIDE tert-Butyl (4-aMinobutyl)carbaMate hydrochloride 4-(tert-Butoxycarbonylamino)butylamine hydrochloride 4-[(tert-butoxycarbonyl)amino]butan-1-aminium chloride
CAS	33545-98-1
EINECS	1312995-182-4
InChI	InChI=1/C9H20N2O2.ClH/c1-9(2,3)13-8(12)11-7-5-4-6-10;/h4-7,10H2,1-3H3,(H,11,12);1H

tert-Butyl (4-aMinobutyl)carbaMate hydrochloride - Physico-chemical Properties

Molecular Formula	C9H21ClN2O2
Molar Mass	224.73
Boling Point	292.9°C at 760 mmHg
Flash Point	130.9°C
Vapor Presure	0.00179mmHg at 25°C
Storage Condition	Inert atmosphere,2-8°C
Sensitive	Easily absorbing moisture

tert-Butyl (4-aMinobutyl)carbaMate hydrochloride - Upstream Downstream Industry

Raw Materials

tert-Butyl N-(4-aminobutyl)carbamate
4-Amino-1-butanol
4-(tert-butoxycarbonyl)butyl methanesulfonate
tert-butyl (4-azidobutyl)carbamate
4-(tert-ButoxycarbonylaMino)-1-butanol
Di-tert-butyl dicarbonate
tert-butyl azidoformate

tert-Butyl (4-aMinobutyl)carbaMate hydrochloride - Introduction

4-[(tert-butoxycarbonyl)amino]butan-1-aminium is an organic compound with the chemical formula C10H20ClNO3. Here are some information about its nature, use, formulation and safety:

Nature:
-Appearance: White crystalline solid
-Melting point: About 104-105 ° C
-Solubility: Soluble in water and alcohol solvents, insoluble in non-polar solvents

Use:
- 4-[(tert-butoxycarbonyl)amino]butan-1-aminium chloride is a commonly used protective amino acid reaction intermediate. The product formed by the protection reaction with the amino group can be prevented from being eliminated or oxidized by other reactions during the chemical synthesis. It plays an important role in the synthesis of peptides and proteins.

Method:
- 4-[(tert-butoxycarbonyl)amino]butan-1-aminium chloride can be obtained by reaction with tert-butyl chloroformate. The specific reaction steps are as follows: firstly, tert-butyl chloroformate is reacted with aminobutanol to generate tert-butoxycarbonylaminobutanol, and then the intermediate is treated with hydrochloric acid to form 4-[(tert-butoxycarbonyl)amino]butan-1-aminium chlorine.

Safety Information:
-Since there is no clear risk information report, 4-[(tert-butoxycarbonyl)amino]butan-1-aminium chloride is less toxic and harmful. However, as a chemical, it is still necessary to follow regular laboratory safety practices and assess the associated hazards and risks on a case-by-case basis. Personal protective equipment should be worn during use, avoid contact with skin and eyes, and ensure adequate ventilation. Any improper use may result in injury or adverse reactions. It is best to use under guidance and look for more detailed information in the safety data sheet.

Last Update：2024-04-10 22:29:15