ACTH (6-9)

Base Information

• Chemical Name: ACTH (6-9)
• CAS No.: 4289-02-5
• Molecular Formula: C32H40 N10 O5
• Molecular Weight: 644.734
• Mol file: 4289-02-5.mol

Synonyms:L-Tryptophan,N-[N2-(N-L-histidyl-L-phenylalanyl)-L-arginyl]-; Tryptophan,N-[N2-(N-L-histidyl-3-phenyl-L-alanyl)-L-arginyl]- (7CI); Tryptophan,N-[N2-(N-L-histidyl-3-phenyl-L-alanyl)-L-arginyl]-, L- (8CI); 13: PN:US20060014676 SEQID: 21 unclaimed sequence; 14: PN: US20050164914 SEQID: 1unclaimed sequence; 17: PN: US20050130901 SEQID: 16 unclaimed sequence; 1: PN:US20030212002 TABLE: 1 unclaimed sequence; 1: PN: US20090069224 SEQID: 1unclaimed sequence; 1: PN: WO0004873 SEQID: 11 unclaimed protein; 207: PN:WO2008033395 SEQID: 219 unclaimed sequence; 233: PN: US20090186020 SEQID: 81unclaimed protein; 238: PN: WO2009134281 SEQID: 81 unclaimed protein; 29: PN:US20090297444 SEQID: 33 unclaimed protein; 2: PN: US20060014194 SEQID: 1unclaimed sequence; 2: PN: WO2006052468 SEQID: 4 unclaimed sequence; 3: PN:US20090305960 SEQID: 3 unclaimed protein; 4: PN: CA2562767 SEQID: 4 unclaimedsequence; 5: PN: US20040086946 SEQID: 1 unclaimed sequence; 63: PN:WO2004075830 SEQID: 63 claimed protein; 81: PN: WO2006047535 SEQID: 81unclaimed sequence; 89: PN: US20040248212 SEQID: 63 unclaimed sequence; 8: PN:WO2005120588 SEQID: 1 claimed sequence; 8: PN: WO2009152079 SEQID: 3 unclaimedsequence; ACTH (6-9); ACTH(6-9)-OH; Hisetal

Chemical Property of ACTH (6-9)

Chemical Property:

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• PSA: 277.96000
• Density: 1.48g/cm³
• LogP: 4.34580

Purity/Quality:

98.5% ^*data from raw suppliers

Characteristic MSH-Tetrapeptide H-His-Phe-Arg-Trp-OH ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of ACTH (6-9)

There total 2 articles about ACTH (6-9) 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:

His-Phe-Arg-Trp-Pro-Gly-Pro → His-Phe-Arg-Trp-Pro-Gly + His-Phe-Arg-Trp (4289-02-5) + L-Tryptophan (73-22-3,27732-43-0,80206-30-0,27813-82-7)

Guidance literature:

With baker’s yeast carboxypeptidase Y; In aq. phosphate buffer; at 30 ℃; Enzymatic reaction;

DOI:10.1134/S1068162016020126

Reference yield:

→ His-Phe-Arg-Trp (4289-02-5)

Guidance literature:

N^α,N^Im-Dicarbobenzoxy-L-histidyl-L-phenylalanyl-N^G-tosyl-L-arginyl-L-tryptophan-benzylester, Natrium, fl. NH3;

DOI:10.1246/bcsj.37.289

Refernces