Carboxypeptidase A

Base Information

• Chemical Name: Carboxypeptidase A
• CAS No.: 11075-17-5
• Molecular Formula: C₄H₁₁NO
• Molecular Weight: 89.1374
• Mol file: 11075-17-5.mol

Synonyms:CarboxypeptidaseA1;Carboxypolypeptidase;E.C. 3.4.12.2;E.C. 3.4.17.1;E.C. 3.4.2.1;

Chemical Property of Carboxypeptidase A

Chemical Property:

• Appearance/Colour: white suspension
• Flash Point: 4 °C
• PSA: 0.00000
• Density: 1.00 g/mL at 20 °C
• LogP: 0.00000
• Storage Temp.: 2-8°C

Purity/Quality:

99% ^*data from raw suppliers

Carboxypeptidase?A from bovine pancreas (Type II-PMSF treated), ≥50?units/mg protein, aqueous suspension ^*data from reagent suppliers

Safty Information:

• Pictogram(s): F, Xn, B, Xi
• Hazard Codes: F,Xn,B,Xi
• Statements: 11-38-42-48/20-63-65-67-36-36/37/38
• Safety Statements: 36/37-45-62-36-26-23-16-24-22

MSDS Files:

Total 1 MSDS from other Authors

Useful:

• Uses: The enzyme from Sigma has been used as a comparison to study the specificity of Metarhizium anisopliae carboxypeptidase A (MeCPA). MeCPA had been genetically engineered to facilitate the removal of polyhistidine tags from the C-termini of recombinant proteins. It has also been used to de-tyrosinate α-tubulin, in vitro, in order to induce high affinity to ethyl-N-phenylcarbamate (EPC) sepharose.

Technology Process of Carboxypeptidase A

There total 26 articles about Carboxypeptidase A 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: 94.0%

oxirane (75-21-8,99932-75-9) + ethylamine (75-04-7,85404-22-4) → 2-(Ethylamino)ethanol (110-73-6)

Guidance literature:

In water; at 35 ℃; for 0.0444444h; Temperature;

Reference yield: 60.0%

2-methyl-4,5-dihydro-1,3-oxazole (1120-64-5,26375-28-0) → 2-(Ethylamino)ethanol (110-73-6) + 2-(Diethylamino)ethanol (100-37-8)

Guidance literature:

With platinum on carbon; hydrogen; at 25 ℃; for 16h; under 7500.75 Torr;

DOI:10.1002/cctc.201701287

Reference yield: 60.0%

2-methyl-4,5-dihydro-1,3-oxazole (1120-64-5,26375-28-0) → 2-(Ethylamino)ethanol (110-73-6)

Guidance literature:

With platinum on carbon; hydrogen; at 25 ℃; for 16h; under 30003 Torr; Autoclave;

upstream raw materials:

oxirane

ethylamine

pyridine

2-(Diethylamino)ethanol

Refernces

• 1、 Boggu, Pulla Reddy,Kim, Youngsoo,Jung, Sang-Hun. "Discovery of benzimidazole analogs as a novel interleukin-5 inhibitors". . . Retrieved 2019/08/12.
• 2、 -. "METHOD FOR PRODUCING 2-(ALKYLAMINO)ETHANOL COMPOUND". Paragraph 0042. . Retrieved 2017/08/24.