N-Octanoyl-4-aminobutyric acid

Base Information

Chemical Name:N-Octanoyl-4-aminobutyric acid
CAS No.:140846-94-2
Molecular Formula:C₁₂H₂₃NO₃
Molecular Weight:229.32
Hs Code.:
UNII:4D2462W14W
Nikkaji Number:J696.641A
Wikidata:Q27259429
Mol file:140846-94-2.mol

Synonyms:N-octanoyl-4-aminobutyric acid;N-octanoyl-GABA;N-octanoyl-gamma-aminobutyric acid;O-GABA

Suppliers and Price of N-Octanoyl-4-aminobutyric acid

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

TRC
4-octanamidobutanoicacid
250mg
$ 310.00

Total 2 raw suppliers

Chemical Property of N-Octanoyl-4-aminobutyric acid

Chemical Property:

Boiling Point:439.3±28.0 °C(Predicted)
PSA：66.40000
Density:1.009±0.06 g/cm3(Predicted)
LogP:2.71880
XLogP3:2.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:10
Exact Mass:229.16779360
Heavy Atom Count:16
Complexity:204

Purity/Quality:

99% ^*data from raw suppliers

4-octanamidobutanoicacid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCCC(=O)NCCCC(=O)O

Technology Process of N-Octanoyl-4-aminobutyric acid

There total 1 articles about N-Octanoyl-4-aminobutyric acid 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:

: 124-07-2
Octanoic acid

: 56-12-2
4-amino-n-butyric acid

: 140846-94-2
N-octanoyl GABA

Guidance literature:: With adenosine monophosphate ligase SfaB from Streptomyces thioluteus; ATP; magnesium chloride; Cleland's reagent; In aq. buffer; at 30 ℃; for 6h; pH=8; Enzymatic reaction;
DOI:10.1002/anie.202010042