| Identification | Back Directory | [Name]
2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride | [CAS]
134979-01-4 | [Synonyms]
AEEA-OH
AEEA.HCl
AEEA-OH·HCl
H-Ado-OH.HCl
2-(2-(2-Aminoethoxy)
CH2COOH-PEG2-NH2.HCl
2-(2-(2-Aminoethoxy)ethoxy)acetic acid HCL
2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride
2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride USP/EP/BP | [Molecular Formula]
C6H14ClNO4 | [MDL Number]
MFCD11865374 | [MOL File]
134979-01-4.mol | [Molecular Weight]
199.633 |
| Chemical Properties | Back Directory | [storage temp. ]
Inert atmosphere,Room Temperature | [Appearance]
White to off-white Solid | [InChI]
InChI=1S/C6H13NO4.ClH/c7-1-2-10-3-4-11-5-6(8)9;/h1-5,7H2,(H,8,9);1H | [InChIKey]
NGPFHPADAGAUDR-UHFFFAOYSA-N | [SMILES]
C(O)(=O)COCCOCCN.[H]Cl |
| Hazard Information | Back Directory | [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].
| [Synthesis]
2-(2-(2-Aminoethoxy)ethoxy)acetic acid hydrochloride was prepared by reacting 2,2-Dimethyl-4-oxo-3,8,11-trioxa-5-azatridecan-13-oic acid with hydrogenchloride in ethyl acetate solution.
 | [References]
[1] ALICE GHIDINI. Synthesis of PNA oligoether conjugates.[J]. Molecules, 2014, 19 3: 3135-3148. DOI:10.3390/molecules19033135. |
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