3,6,9,12,15-Pentaoxaheptadecanoic acid, 17-azido-

Base Information

Chemical Name:3,6,9,12,15-Pentaoxaheptadecanoic acid, 17-azido-
CAS No.:217180-81-9
Molecular Formula:C₁₂H₂₃N₃O₇
Molecular Weight:321.331
Hs Code.:
Mol file:217180-81-9.mol

Synonyms:N3-PEG5-CH2COOH;N3-PEG5-CH2CO2H;Azido-PEG5-CH2CO2H;AZIDE-PEG5-CH2COOH;Azido-PEG5-CH2COOH;17-azido-3,6,9,12,15-pentaoxaheptadecanoic acid

Suppliers and Price of 3,6,9,12,15-Pentaoxaheptadecanoic acid, 17-azido-

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

purepeg
N3-PEG5-CH2COOH min.97%
1 g
$ 504.00

BroadPharm
Azido-PEG5-CH2CO2H 98%
500 MG
$ 380.00

BroadPharm
Azido-PEG5-CH2CO2H 98%
1 G
$ 570.00

Activate Scientific
N3-PEG5-CH2COOH 95+%
1 g
$ 588.00

Acrotein
N3-PEG5-CH2COOH 97%
1g
$ 495.00

Acrotein
N3-PEG5-CH2COOH 97%
0.5g
$ 330.00

Acrotein
N3-PEG5-CH2COOH 97%
0.25g
$ 220.00

Total 20 raw suppliers

Chemical Property of 3,6,9,12,15-Pentaoxaheptadecanoic acid, 17-azido-

Chemical Property:

Purity/Quality:

97% ^*data from raw suppliers

N3-PEG5-CH2COOH min.97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Description Azido-PEG5-CH2CO2H is a water soluble PEG linker. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide.

Technology Process of 3,6,9,12,15-Pentaoxaheptadecanoic acid, 17-azido-

There total 18 articles about 3,6,9,12,15-Pentaoxaheptadecanoic acid, 17-azido- 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: 96.0%

: C₁₃H₂₅N₃O₇

: 217180-81-9
17-Azido-3,6,9,12,15-pentaoxaheptadecanoic acid

Guidance literature:: With water; sodium hydroxide; In methanol; at 0 - 20 ℃; for 3h;

Reference yield: 89.0%

: 86770-69-6
17-azido-3,6,9,12,15-pentaoxaheptadecan-1-ol

: 217180-81-9
17-Azido-3,6,9,12,15-pentaoxaheptadecanoic acid

Guidance literature:: With Jones reagent; In acetone; at -5 - 20 ℃; for 2h; Inert atmosphere;

Reference yield:

: 86770-68-5
2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethanol

: 79-08-3
bromoacetic acid

: 217180-81-9
17-Azido-3,6,9,12,15-pentaoxaheptadecanoic acid

Guidance literature:: 14-azido-3,6,9,12-tetraoxatetradecan-1-ol; With sodium hydride; In tetrahydrofuran; mineral oil; at 0 - 20 ℃; for 1h;

bromoacetic acid; In tetrahydrofuran; mineral oil; at 0 - 20 ℃; for 16h;
DOI:10.1016/j.bmc.2022.116707