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01840

Sigma-Aldrich

Adenine monohydrochloride

≥99.0% (HPLC)

Synonym(s):

Adenine hydrochloride

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About This Item

Empirical Formula (Hill Notation):
C5H5N5 · HCl
CAS Number:
2922-28-3
Molecular Weight:
171.59
Beilstein:
4009585
EC Number:
220-867-0
MDL number:
MFCD00075782
UNSPSC Code:
12352100
PubChem Substance ID:
329747363
NACRES:
NA.22
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Quality Level

200

Assay

≥99.0% (HPLC)

loss

≤5% loss on drying

mp

~285 °C (dec.)

SMILES string

Cl[H].Nc1ncnc2[nH]cnc12

InChI

1S/C5H5N5.ClH/c6-4-3-5(9-1-7-3)10-2-8-4;/h1-2H,(H3,6,7,8,9,10);1H

InChI key

UQVDQSWZQXDUJB-UHFFFAOYSA-N

Related Categories

Application

Adenine monohydrochloride can be used in designing novel bioactive adenine derivatives[1][2] and adenine-based polyimide/nano-silica hybrid films[3].

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF4875V
WXBF3433V
WXBD9914V
WXBD9101V
WXBD7071V

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Preparation and characterization of adenine-based polyimide/nano-silica hybrid films
Lu Z, et al.
European Polymer Journal, 102, 209-218 (2018)
Synthesis and DNA binding of new adenine derivatives incorporating 5-((Alkylthio)-1,3,4-oxadiazol-2-yl) methyl moiety
Y?lmaz Y, et al.
Medicinal Chemistry Research, 27(8), 2027-2033 (2018)
Synthesis of triazolylmethyl-linked nucleoside analogs via combination of azidofuranoses with propargylated nucleobases and study on their cytotoxicity
Halay E, et al.
Chemistry of Heterocyclic Compounds, 1-9 (2018)
Shi Chen et al.
Nanoscale, 12(5), 3302-3307 (2020-01-24)
Self-assembly of nucleic acid nanostructures is driven by selective association of oligonucleotide modules through base pairing between complementary sequences. Herein, we report the development of RNA-DNA hybrid nanoshapes that conditionally assemble under the control of an adenosine ligand. The design

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