Arginyllysine

Base Information

Chemical Name:Arginyllysine
CAS No.:40968-46-5
Molecular Formula:C₁₂H₂₆N₆O₃
Molecular Weight:302.377
Hs Code.:2925290090
DSSTox Substance ID:DTXSID80423793
Nikkaji Number:J1.390.552E
Wikidata:Q27144132
Metabolomics Workbench ID:78687
ChEMBL ID:CHEMBL380024
Mol file:40968-46-5.mol

Synonyms:Arg-Lys;arginine-lysine;arginyllysine

Suppliers and Price of Arginyllysine

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

Biosynth Carbosynth
H-Arg-Lys-OH acetate salt
500 mg
$ 355.00

Biosynth Carbosynth
H-Arg-Lys-OH acetate salt
250 mg
$ 205.00

Biosynth Carbosynth
H-Arg-Lys-OH acetate salt
100 mg
$ 102.00

Biosynth Carbosynth
H-Arg-Lys-OH acetate salt
2 g
$ 1071.30

Biosynth Carbosynth
H-Arg-Lys-OH acetate salt
1 g
$ 616.00

American Custom Chemicals Corporation
ARG-LYS-OH ACETATE SALT 98.00%
5MG
$ 496.83

Total 11 raw suppliers

Chemical Property of Arginyllysine

Chemical Property:

PSA：217.64000
LogP:1.34870
Storage Temp.:-15°C
XLogP3:-4.7
Hydrogen Bond Donor Count:6
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:11
Exact Mass:302.20663871
Heavy Atom Count:21
Complexity:357

Purity/Quality:

99% ^*data from raw suppliers

H-Arg-Lys-OH acetate salt ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(CCN)CC(C(=O)O)NC(=O)C(CCCN=C(N)N)N
Isomeric SMILES:C(CCN)C[C@@H](C(=O)O)NC(=O)[C@H](CCCN=C(N)N)N

Technology Process of Arginyllysine

There total 6 articles about Arginyllysine 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:

: (S)-6-Benzyloxycarbonylamino-2-((S)-2-benzyloxycarbonylamino-5-guanidino-pentanoylamino)-hexanoic acid; hydrochloride

: 40968-46-5
Arg-Lys

Guidance literature:: With hydrogen; acetic acid; palladium; In methanol;
DOI:10.1139/v60-262

Reference yield:

: 97615-54-8
Cbo-nitro-L-Arg-ε-Cbo-L-Lys-benzylester

: 40968-46-5
Arg-Lys

Guidance literature:: With hydrogen; palladium; In methanol; water; acetic acid;

Reference yield:

: 2149-70-4,13855-78-2,38733-00-5
N-nitro-L-arginine

: 40968-46-5
Arg-Lys

Guidance literature:: Multi-step reaction with 3 steps

1: aq. NaOH

2: (i) Et₃N, THF, DMF, (ii) /BRN= 2548552/, DCC

3: H₂ / Pd / methanol; acetic acid; H₂O

With sodium hydroxide; hydrogen; palladium; In methanol; water; acetic acid;