N-Fmoc-5-aminolevulinic acid

Base Information

Chemical Name:N-Fmoc-5-aminolevulinic acid
CAS No.:160111-41-1
Molecular Formula:C20H19 N O5
Molecular Weight:353.375
Hs Code.:2922499990
Mol file:160111-41-1.mol

Synonyms:N-Fmoc-5-aminolevulinic acid;5-(((9H-Fluoren-9-yl)methoxy)carbonylamino)-4-oxopentanoic acid

Suppliers and Price of N-Fmoc-5-aminolevulinic 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

Matrix Scientific
Fmoc-5-aminolevulinic acid
1g
$ 410.00

Matrix Scientific
Fmoc-5-aminolevulinic acid
5g
$ 1230.00

American Custom Chemicals Corporation
FMOC-5-AMINOLEVULINIC ACID 95.00%
5G
$ 3109.26

American Custom Chemicals Corporation
FMOC-5-AMINOLEVULINIC ACID 95.00%
1G
$ 993.30

AK Scientific
Fmoc-5-aminolevulinicacid
1g
$ 603.00

Acrotein
5-(Fmoc-amino)-4-oxo-pentanoicacid 97%
0.5g
$ 247.50

Total 11 raw suppliers

Chemical Property of N-Fmoc-5-aminolevulinic acid

Chemical Property:

Boiling Point:606.4±40.0 °C(Predicted)
PKA:4.59±0.17(Predicted)
PSA：92.70000
Density:1.296±0.06 g/cm3(Predicted)
LogP:3.34990
Storage Temp.:2-8°C

Purity/Quality:

97% ^*data from raw suppliers

Fmoc-5-aminolevulinic acid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of N-Fmoc-5-aminolevulinic acid

There total 4 articles about N-Fmoc-5-aminolevulinic 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:

: C₂₀H₁₇NO₅

: 160111-41-1
Fmoc-ALA-OH

Guidance literature:: With hydrogen bromide; acetic acid; at 100 ℃; for 1h; Inert atmosphere;

Reference yield:

: 28920-43-6
(fluorenylmethoxy)carbonyl chloride

: 160111-41-1
Fmoc-ALA-OH

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / dichloromethane / 0.5 h / 0 °C

2: sodium dihydrogenphosphate; chlorine dioxyde / water; butan-1-ol / 3 h / 0 °C

3: acetic acid; hydrogen bromide / 1 h / 100 °C / Inert atmosphere

With sodium dihydrogenphosphate; chlorine dioxyde; hydrogen bromide; potassium carbonate; acetic acid; In dichloromethane; water; butan-1-ol;

Reference yield:

: C₂₀H₁₇NO₃

: 160111-41-1
Fmoc-ALA-OH

Guidance literature:: Multi-step reaction with 2 steps

1: sodium dihydrogenphosphate; chlorine dioxyde / water; butan-1-ol / 3 h / 0 °C

2: acetic acid; hydrogen bromide / 1 h / 100 °C / Inert atmosphere

With sodium dihydrogenphosphate; chlorine dioxyde; hydrogen bromide; acetic acid; In water; butan-1-ol;