Aspartylglutamate

Base Information

Chemical Name:Aspartylglutamate
CAS No.:6157-06-8
Molecular Formula:C9H14 N2 O7
Molecular Weight:262.219
Hs Code.:2924199090
DSSTox Substance ID:DTXSID50977157
Nikkaji Number:J81.155F
Wikidata:Q27144146
Metabolomics Workbench ID:78722
ChEMBL ID:CHEMBL420850
Mol file:6157-06-8.mol

Synonyms:Asp-Glu;aspartylglutamate

Suppliers and Price of Aspartylglutamate

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-Asp-Glu-OH
2 g
$ 464.00

Biosynth Carbosynth
H-Asp-Glu-OH
1 g
$ 273.00

Biosynth Carbosynth
H-Asp-Glu-OH
10 g
$ 1613.90

Biosynth Carbosynth
H-Asp-Glu-OH
5 g
$ 928.00

Biosynth Carbosynth
H-Asp-Glu-OH
500 mg
$ 155.00

American Custom Chemicals Corporation
L-ASPARTIC ACID-L-GLUTAMIC ACID 98.00%
5G
$ 1761.38

AK Scientific
Asp-glu
1g
$ 657.00

AK Scientific
Asp-glu
100mg
$ 185.00

Total 12 raw suppliers

Chemical Property of Aspartylglutamate

Chemical Property:

Vapor Pressure:1.89E-18mmHg at 25°C
Melting Point:150-155℃
Boiling Point:647.8°C at 760 mmHg
PKA:2.86±0.10(Predicted)
Flash Point:345.6°C
PSA：167.02000
Density:1.53g/cm³
LogP:-0.68620
Storage Temp.:−20°C
XLogP3:-4.6
Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:8
Rotatable Bond Count:8
Exact Mass:262.08010079
Heavy Atom Count:18
Complexity:355

Purity/Quality:

98%Min ^*data from raw suppliers

H-Asp-Glu-OH ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Aspartylglutamate

There total 6 articles about Aspartylglutamate 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:

: 73618-80-1
N-(N-benzyloxycarbonyl-L-α-aspartyl)-L-glutamic acid

: 6157-06-8
L-aspartyl-L-glutamic acid

Guidance literature:: With methanol; palladium; Hydrogenation;
DOI:10.1039/jr9520000024

Reference yield:

: 104870-27-1
N-(O-benzyl-N-benzyloxycarbonyl-L-α-aspartyl)-L-glutamic acid dibenzyl ester

: 6157-06-8
L-aspartyl-L-glutamic acid

Guidance literature:: With methanol; palladium; Hydrogenation;
DOI:10.1039/jr9520000024

Reference yield:

: 16450-41-2
L-glutamic acid diethyl ester

: 6157-06-8
L-aspartyl-L-glutamic acid

Guidance literature:: Multi-step reaction with 3 steps

1: ethyl acetate

2: aqueous NaOH

3: palladium; aqueous methanol / Hydrogenation

With methanol; sodium hydroxide; palladium; ethyl acetate;
DOI:10.1039/jr9520000024