L-Threoninol
(2R,3R)-2-aminobutane-1,3-diol
Product summary
Quick view
- Product family
- Oligonucleotide Synthesis, RNA Raw Materials & Modification
- Chemical Name
- (2R,3R)-2-aminobutane-1,3-diol
- MF
- C4H11NO2
- MW
- 105.14
- Purity
- 99.5%
L-Threoninol is a chiral amino alcohol identified as (2R,3R)-2-aminobutane-1,3-diol. It is also indexed as threoninol, H-threoninol, reduced threonine, and (2R,3R)-2-amino-1,3-butanediol.
CH59016 is listed with CAS 3228-51-1, molecular formula C4H11NO2, and molecular weight 105.14. Research literature links L-threoninol with acyclic L-threoninol nucleic acid scaffold chemistry, L-aTNA phosphoramidite monomer and chemical-ligation method studies, and chiral fluorescent recognition of threoninol.
Synonyms
Threoninol; H-Threoninol; Reduced Threonine; (2R,3R)-2-Amino-1,3-butanediol; 1,3-Butanediol, 2-amino-, (2R,3R)-
Identity and specifications
| Catalog No. | CH59016 |
| CAS No. | 3228-51-1 |
| Molecular Formula | C4H11NO2 |
| Molecular Weight | 105.14 |
| PubChem CID | 2033049 |
| InChIKey | MUVQIIBPDFTEKM-QWWZWVQMSA-N |
| Purity | 99.5% |
Storage conditions
-20 C
Technical attributes
- Scaffold class
- Chiral amino diol
- Stereochemistry
- (2R,3R)
- Functional groups
- Primary amine and 1,3-diol
- Research role
- L-aTNA scaffold precursor
- Grade
- 97% product designation
- Packaging
- 1 g product code; Custom packaging on request
- Physical form
- Liquid
Application context
- L-aTNA scaffold chemistry: reported in artificial nucleic acid studies involving acyclic L-threoninol nucleic acid cross-pairing with DNA and RNA.
- Monomer and ligation methods: relevant to L-aTNA phosphoramidite monomer synthesis and chemical-ligation method research.
- Chiral recognition: reported in fluorescent probe studies for selective recognition of threoninol.
Related technical resources
Oligonucleotide Modification
Sugar, base, backbone, terminal, and conjugation modifications for ASO, siRNA, guide RNA, aptamer, and research or labeling oligo projects.
Oligonucleotide Synthesis
Support for modified monomers, supports, sulfurizing reagents, cap analogs, and related oligo synthesis inputs.
Public references
- Sustainability Challenges and Opportunities in Oligonucleotide Manufacturing
Journal of Organic Chemistry, 2021
Product-family technical context
- Solid-phase supports for oligonucleotide synthesis
Current Protocols in Nucleic Acid Chemistry, 2013
Product-family technical context
- Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesis
Tetrahedron Letters, 1981
Product-family technical context
- Synthesis of deoxyoligonucleotides on a polymer support
Journal of the American Chemical Society, 1981
Product-family technical context
- PubChem Compound 2033049
PubChem · CID 2033049
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