13-Aminotridecanoic acid

Base Information

Chemical Name:13-Aminotridecanoic acid
CAS No.:17437-19-3
Molecular Formula:C13H27NO2
Molecular Weight:229.363
Hs Code.:
Mol file:17437-19-3.mol

Synonyms:13-Aminotridecanoic acid

Suppliers and Price of 13-Aminotridecanoic 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
13-AminotridecanoicAcid
50mg
$ 195.00

Total 4 raw suppliers

Chemical Property of 13-Aminotridecanoic acid

Chemical Property:

Melting Point:174 - 175 °C (H2O)
PSA：63.32000
LogP:4.02110

Purity/Quality:

97%min ^*data from raw suppliers

13-AminotridecanoicAcid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Uses 13-Aminotridecanoic Acid is used for preparation and HIV-1 inhibitory activity of betulinic acid ω-aminoalkanoic acid derivatives.

Technology Process of 13-Aminotridecanoic acid

There total 8 articles about 13-Aminotridecanoic 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:

: C₂₀H₃₉NO₃

: 17437-19-3
13-aminotridecaneoic acid

: 111-26-2
hexan-1-amine

: 111-14-8
oenanthic acid

: 505-52-2
brassylic acid

Guidance literature:: C₂₀H₃₉NO₃; With sulfuric acid; at 100 ℃; for 2h;

With water; sodium hydroxide; for 5h; Autoclave;

Reference yield:

: (11Z,14R)-14-hydroxyicos-11-enoic acid

: 17437-19-3
13-aminotridecaneoic acid

Guidance literature:: With L-alanin; sodium hydroxide; In aq. buffer; at 35 ℃; for 2h; pH=8 - 9.5; Enzymatic reaction;
DOI:10.1002/adsc.201300784