FMOC-15-AMINO-4,7,10,13-TETRAOXAPENTADECANOIC ACID

Base Information

Chemical Name:FMOC-15-AMINO-4,7,10,13-TETRAOXAPENTADECANOIC ACID
CAS No.:557756-85-1
Molecular Formula:C₂₆H₃₃NO₈
Molecular Weight:487.55
Hs Code.:29225090
Mol file:557756-85-1.mol

Synonyms:FMOC-15-AMINO-4,7,10,13-TETRAOXAPENTADECANOIC ACID

Suppliers and Price of FMOC-15-AMINO-4,7,10,13-TETRAOXAPENTADECANOIC 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

SynChem
Fmoc-NH-PEG4-CH2CH2COOH 95%
1 g
$ 260.00

purepeg
Fmoc-15-amino-4,7,10,13-tetraoxapentadecacanoicacid min.97%
1 g
$ 167.00

purepeg
Fmoc-15-amino-4,7,10,13-tetraoxapentadecacanoicacid min.97%
5 g
$ 469.00

Matrix Scientific
1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13,16-pentaoxa-4-azanonadecan-19-oic acid
5g
$ 422.00

Iris Biotech GmbH
Fmoc-NH-PEG(4)-COOH
1 g
$ 236.25

Iris Biotech GmbH
Fmoc-NH-PEG(4)-COOH
5 g
$ 675.00

Frontier Specialty Chemicals
Fmoc-15-amino-4,7,10,13-tetraoxapentadecanoicacid
1g
$ 1180.00

Frontier Specialty Chemicals
Fmoc-15-amino-4,7,10,13-tetraoxapentadecanoicacid
250mg
$ 701.00

Frontier Specialty Chemicals
Fmoc-15-amino-4,7,10,13-tetraoxapentadecanoicacid
100mg
$ 438.00

dPEG
Fmoc-N-amido-dPEG??-acid
100 mg
$ 100.00

Total 38 raw suppliers

Chemical Property of FMOC-15-AMINO-4,7,10,13-TETRAOXAPENTADECANOIC ACID

Chemical Property:

Boiling Point:682.1±55.0 °C(Predicted)
PKA:4.28±0.10(Predicted)
PSA：112.55000
Density:1.219
LogP:3.45710
Storage Temp.:-20°C
Solubility.:Soluble in DMSO, DCM, DMF

Purity/Quality:

98%,99%, ^*data from raw suppliers

Fmoc-NH-PEG4-CH2CH2COOH 95% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: 24/25

MSDS Files:: SDS file from LookChem

Useful:

Description Fmoc-N-amido-PEG4-acid is a PEG linker containing an Fmoc-protected amine and a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. 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 bond.

Technology Process of FMOC-15-AMINO-4,7,10,13-TETRAOXAPENTADECANOIC ACID

There total 3 articles about FMOC-15-AMINO-4,7,10,13-TETRAOXAPENTADECANOIC 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: 80.0%

: 1-amino-3,6,9,12-tetraoxapentadecan-15-oic acid hydrochloride

: 82911-69-1
N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide

: 557756-85-1,850312-72-0
3-[2-[2-[2-[2-(9H-fluoren-9-ylmethoxycarbonylamino)ethoxy]ethoxy]ethoxy]ethoxy]propanoic acid

Guidance literature:: 1-amino-3,6,9,12-tetraoxapentadecan-15-oic acid hydrochloride; With sodium hydrogencarbonate; In tetrahydrofuran; water; at 20 ℃; for 0.333333h;

N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide; In tetrahydrofuran; water; at 0 - 20 ℃;