2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride
- Product Name2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride
- CAS134979-01-4
- CBNumberCB82128643
- MFC6H14ClNO4
- MW199.63266
- MDL NumberMFCD11865374
- MOL File134979-01-4.mol
- MSDS FileSDS
Chemical Properties
storage temp. | Inert atmosphere,Room Temperature |
2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride Price
Product number | Packaging | Price | Product description | Buy |
---|---|---|---|---|
TRC A619488 | 10mg | $45 | 2-(2-(2-Aminoethoxy)Ethoxy)AceticAcidHydrochloride |
Buy |
Biosynth Carbosynth FA142212 | 500mg | $125 | 2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride |
Buy |
Biosynth Carbosynth FA142212 | 1g | $200 | 2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride |
Buy |
Biosynth Carbosynth FA142212 | 5G | $400 | 2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride |
Buy |
American Custom Chemicals Corporation CHM0387518 | 5MG | $505.56 | 2-(2-(2-AMINOETHOXY)ETHOXY)ACETIC ACID HYDROCHLORIDE 95.00% |
Buy |
2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride Chemical Properties,Usage,Production
Uses
2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride is an amino acid derivative salt reagent with an amino and carboxyl group at each end of its molecular structure, which can be used in the field of nucleic acid sequencing. It can also be used as a component for the synthesis of PNA oligoether conjugates. Single and double conjugation of 2-(2-(2-aminoethoxy)ethoxy)ethanol was obtained using carbonyldiimidazole. Multiple attachment of 2-(2-(2-(benzoyloxy)ethoxy)ethoxy)acetic acid building blocks to the N-terminus and β-amino groups of inserted diaminopropionic acid residues was achieved using a post-PNA assembly coupling procedure[1].References
[1] ALICE GHIDINI. Synthesis of PNA oligoether conjugates.[J]. Molecules, 2014, 19 3: 3135-3148. DOI:10.3390/molecules19033135.Preparation Products And Raw materials
Preparation Products
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