2-AMINO-2-METHYLBUTYRIC ACID

Base Information

Chemical Name:2-AMINO-2-METHYLBUTYRIC ACID
CAS No.:465-58-7
Molecular Formula:C5H11NO2
Molecular Weight:117.15
Hs Code.:
Mol file:465-58-7.mol

Synonyms:2-AMINO-2-METHYL-BUTYRIC ACID, RAC;2-AMINO-2-METHYLBUTYRIC ACID;ISOVALINE

Suppliers and Price of 2-AMINO-2-METHYLBUTYRIC ACID

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Usbiological
2-Amino-2-methylbutyric acid
100mg
$ 305.00

American Custom Chemicals Corporation
2-AMINO-2-METHYLBUTYRIC ACID 95.00%
5G
$ 1421.65

American Custom Chemicals Corporation
2-AMINO-2-METHYLBUTYRIC ACID 95.00%
2.5G
$ 1147.43

American Custom Chemicals Corporation
2-AMINO-2-METHYLBUTYRIC ACID 95.00%
1G
$ 808.89

Total 35 raw suppliers

Chemical Property of 2-AMINO-2-METHYLBUTYRIC ACID

Chemical Property:

Boiling Point:213.6°Cat760mmHg
Flash Point:83°C
PSA：63.32000
Density:1.07g/cm³
LogP:0.89870

Purity/Quality:

97% ^*data from raw suppliers

2-Amino-2-methylbutyric acid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses a-Me-Gly(Ethyl)-OH is used in preparation of peptide compound comprising highly sterically hindered amino acid via reaction of electron-withdrawing group-protected N-unsubstituted-α,α-disubstituted amino acid with peptide followed by N-alkylation.

Technology Process of 2-AMINO-2-METHYLBUTYRIC ACID

There total 82 articles about 2-AMINO-2-METHYLBUTYRIC ACID which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

: 139937-98-7
N-(tert-butoxycarbonyl)-2-amino-2-methylbutanoic acid

: 595-39-1,465-58-7
DL-isovaline

Guidance literature:: N-(tert-butoxycarbonyl)-2-amino-2-methylbutanoic acid; With methanesulfonic acid; In dichloromethane; at 25 ℃; for 0.5h;

With triethylamine; In dichloromethane; at 25 ℃; for 0.166667h;