Septide

Base Information

Chemical Name:Septide
CAS No.:79775-19-2
Molecular Formula:C39H53 N7 O7 S
Molecular Weight:763.959
Hs Code.:
European Community (EC) Number:617-504-7
Nikkaji Number:J356.952G
Wikidata:Q27088782
ChEMBL ID:CHEMBL1885865
Mol file:79775-19-2.mol

Synonyms:6-Glp-9-Pro-substance P (6-11);Glp-Phe-Phe-Pro-Leu-Met-NH2;pGlu(6)-Pro(9)-SP(6-11);pGlu-Phe-Phe-Pro-Leu-Met-NH2;septide;septide, (D-Pro)-isomer;substance P (6-11), Glp(6)-Pro(9)-;substance P (6-11), pyroglutamyl(6)-proline(9)-

Suppliers and Price of Septide

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

American Custom Chemicals Corporation
SEPTIDE 95.00%
5MG
$ 765.00

American Custom Chemicals Corporation
SEPTIDE 95.00%
1MG
$ 505.00

Total 14 raw suppliers

Chemical Property of Septide

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:1189.4°C at 760 mmHg
Flash Point:673.1°C
PSA：357.57000
Density:1.255g/cm³
LogP:-0.92850
Storage Temp.:-15°C
XLogP3:2.8
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:19
Exact Mass:763.37271823
Heavy Atom Count:54
Complexity:1320

Purity/Quality:

99%, ^*data from raw suppliers

SEPTIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)CC(C(=O)NC(CCSC)C(=O)N)NC(=O)C1CCCN1C(=O)C(CC2=CC=CC=C2)NC(=O)C(CC3=CC=CC=C3)NC(=O)C4CCC(=O)N4
Isomeric SMILES:CC(C)C[C@@H](C(=O)N[C@@H](CCSC)C(=O)N)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@H](CC3=CC=CC=C3)NC(=O)[C@@H]4CCC(=O)N4

Technology Process of Septide

There total 16 articles about Septide 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:

: C₁₀H₁₅NO₅

: 101760-43-4
Phe-Phe-Pro-Leu-Met-NH₂*HCl

: 79775-19-2
Septide

Guidance literature:: With 4-methyl-morpholine; In N,N-dimethyl-formamide; at -20 ℃; for 2h; Yield given;
DOI:10.1021/jm00157a029

Reference yield:

: C₁₉H₂₇NO₆

: 79775-19-2
Septide

Guidance literature:: Multi-step reaction with 5 steps

1: N-methylmorpholine, hexamethylphosphoric acid triamide / dimethylformamide / 2 h / -20 °C

2: 89 percent / 1 N HCl / acetic acid / 0.5 h / Ambient temperature

3: N-methylmorpholine / dimethylformamide / 2 h / -20 °C

4: 95 percent / 1 N HCl / acetic acid / 0.5 h / Ambient temperature

5: N-methylmorpholine / dimethylformamide / 2 h / -20 °C

With 4-methyl-morpholine; hydrogenchloride; N,N,N,N,N,N-hexamethylphosphoric triamide; In acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/jm00157a029

Reference yield:

: 15761-39-4,59433-50-0
1-(tert-butoxycarbonyl)-L-proline

: 79775-19-2
Septide

Guidance literature:: Multi-step reaction with 8 steps

1: N-methylmorpholine / dimethylformamide / 0.03 h / -20 °C

2: N-methylmorpholine / dimethylformamide / 2 h / -20 °C

3: 95 percent / 1 N HCl / acetic acid / 0.5 h / Ambient temperature

4: N-methylmorpholine, hexamethylphosphoric acid triamide / dimethylformamide / 2 h / -20 °C

5: 89 percent / 1 N HCl / acetic acid / 0.5 h / Ambient temperature

6: N-methylmorpholine / dimethylformamide / 2 h / -20 °C

7: 95 percent / 1 N HCl / acetic acid / 0.5 h / Ambient temperature

8: N-methylmorpholine / dimethylformamide / 2 h / -20 °C

With 4-methyl-morpholine; hydrogenchloride; N,N,N,N,N,N-hexamethylphosphoric triamide; In acetic acid; N,N-dimethyl-formamide;
DOI:10.1021/jm00157a029