Butyric acid, 2-amino-4-sulfo-

Base Information

• Chemical Name: Butyric acid, 2-amino-4-sulfo-
• CAS No.: 1001-13-4
• Molecular Formula: C₄H₉NO₅S
• Molecular Weight: 183.185
• Mol file: 1001-13-4.mol

Synonyms:

Chemical Property of Butyric acid, 2-amino-4-sulfo-

Chemical Property:

• PSA: 126.07000
• LogP: 0.45730

Purity/Quality:

98%,99%, ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of Butyric acid, 2-amino-4-sulfo-

There total 12 articles about Butyric acid, 2-amino-4-sulfo- 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:

formic acid (64-18-6) + L-methionine (63-68-3,26062-47-5,58576-49-1) → L-methionine sulfoxide (3226-65-1,86631-49-4,779988-65-7) + L-glutamic acid (56-86-0,21675-62-7,23009-64-5,25104-13-6,84960-48-5,25513-46-6) + L-methionine sulfone (7314-32-1,1118-85-0) + L-homocysteic acid (14857-77-3,1001-13-4)

Guidance literature:

With hydrogen; oxygen; In water; at 40 - 50 ℃; Further byproducts given; a flame from a burner fed with H₂+O₂ was blown to the surface of an aq. solution; H₂:O₂=83:17;

DOI:10.1016/S0040-4039(97)10802-4

Reference yield:

L-methionine (63-68-3,26062-47-5,58576-49-1) → L-2-aminobutyric acid (1492-24-6) + L-homoserine (672-15-1,119736-88-8) + L-Aspartic acid (56-84-8,25608-40-6,27881-03-4,32505-46-7,52526-39-3) + L-methionine sulfoxide (3226-65-1,86631-49-4,779988-65-7) + L-methionine sulfone (7314-32-1,1118-85-0) + L-homocysteic acid (14857-77-3,1001-13-4)

Guidance literature:

With hydrogen; oxygen; In water; at 40 - 50 ℃; Product distribution; Mechanism; A flame from a burner fed with H₂-O₂ mixtures of different compositions were blown onto the surface of an aq. solution of pH=3;

DOI:10.1016/S0040-4039(97)10802-4

Reference yield:

formic acid (64-18-6) + L-methionine (63-68-3,26062-47-5,58576-49-1) → L-homoserine (672-15-1,119736-88-8) + L-Aspartic acid (56-84-8,25608-40-6,27881-03-4,32505-46-7,52526-39-3) + L-methionine sulfoxide (3226-65-1,86631-49-4,779988-65-7) + L-glutamic acid (56-86-0,21675-62-7,23009-64-5,25104-13-6,84960-48-5,25513-46-6) + L-methionine sulfone (7314-32-1,1118-85-0) + L-homocysteic acid (14857-77-3,1001-13-4)

Guidance literature:

With hydrogen; oxygen; In water; at 40 - 50 ℃; Product distribution; Mechanism; A flame from a burner fed with H₂-O₂ mixtures of different compositions were blown onto the surface of an aq. solution of pH=3;

DOI:10.1016/S0040-4039(97)10802-4

upstream raw materials:

DL-homocystine

water

dihydrogen peroxide

bromine

Downstream raw materials:

C₃₅H₄₅N₄O₆S⁽¹⁺⁾

Refernces

• 1、 Nomoto, Shinya,Shimoyama, Akira,Shiraishi, Susumu. "Flame-induced reactions of sulfur-containing amino acids in an aqueous solution". . p. 1009 - 1012. Retrieved 1998.
• 2、 -. "GLUCAGON/GLP-1 RECEPTOR CO-AGONISTS". . . Retrieved 2010/08/07.