Skip to Content
Merck
CN

L8638

Long chain alkylamine controlled pore glass

120-200 mesh, nominal diameter 500 Å

Synonym(s):

LCAA-CPG

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

UNSPSC Code:
12352200
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

particle size

120-200 mesh

pore size

500 Å nominal diameter

Application

Long chain alkylamine controlled pore glass is used in chromatography. Long chain alkylamine controlled pore glass has been used to develop a novel method for the immobilization of nucleotides and for the synthesis of DNA oligonucleotides and their 3′- or (3′,5′)-conjugates.

Other Notes

Ligand is mixture of primary and secondary alkylamines, approx. 1:1.

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Caren L Freel Meyers et al.
Organic letters, 5(3), 341-344 (2003-01-31)
[reaction: see text] A novel method for the immobilization of nucleotides has been developed. The strategy employs a highly reactive pyrrolidinium phosphoramidate zwitterion intermediate that undergoes nucleophilic attack by long-chain alkylamine-controlled pore glass (LCAA-CPG) to generate an immobilized nucleotide. Quantification
Andrzej Grajkowski et al.
Bioconjugate chemistry, 19(8), 1696-1706 (2008-07-24)
The functionalization of long chain alkylamine controlled-pore glass (CPG) with a 3-hydroxypropyl-(2-cyanoethyl)thiophosphoryl linker and its conversion to the support 7 has led to the synthesis of DNA oligonucleotides and their 3'- or (3',5')-conjugates. Indeed, CPG support 7 has been successfully
Release of DNA oligonucleotides and their conjugates from controlled-pore glass under thermolytic conditions
Grajkowski, A., et al.
Current Protocols in Nucleic Acid Chemistry / Edited By Serge L. Beaucage ... [Et Al.], 3-3 (2008)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service