(S)-2-Aminobutyramide-d3 Hydrochloride

Product Name (S)-2-Aminobutyramide-d3 Hydrochloride
CAT No. CS-T-64627
CAS No. 1217605-54-3
Category Stable Isotopes
Stock Enquire
Mol. Wt. Not Available
Mol. For. Not Available
Hazardous This is not a Hazardous Compound
COA View Sample COA
MSDS View Sample MSDS
Smileys CCC(C(=O)N)N.Cl
Canonical Smiles CCC(C(=O)N)N.Cl
InchIKey HDBMIDJFXOYCGK-YUKGPTQOSA-N
Inchl InChI=1S/C4H10N2O.ClH/c1-2-3(5)4(6)7;/h3H,2,5H2,1H3,(H2,6,7);1H/t3-;/m0./s1/i1D3;
IUPAC (2S)-2-amino-4,4,4-trideuteriobutanamide;hydrochloride
Controlled No
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(S)-2-Aminobutyramide-d3 Hydrochloride is a deuterated form of S-2-Aminobutyramide Hydrochloride, which is a chemical compound used in biochemical research. It is a stable isotope-labeled compound that is used in proteomics and metabolomics research where it is used as a reference standard in mass spectrometry. (S)-2-Aminobutyramide-d3 Hydrochloride is a chiral molecule that is optically active and exists in two enantiomers, the (R) and (S) forms. The deuterated form replaces three hydrogen atoms with deuterium atoms, which imparts the compound with unique chemical properties that make it useful in scientific research. The deuterium substitution can be used to differentiate between the (R) and (S) enantiomers, which is particularly useful in studying stereochemistry. The compound is typically used as a reference standard in the analysis of biological samples. It is used to calibrate mass spectrometers and to identify and quantify small molecules in complex mixtures. Its utility lies in its ability to provide accurate and precise measurements, which are essential in the development of new drugs and in understanding the metabolic pathways of living organisms. In summary, (S)-2-Aminobutyramide-d3 Hydrochloride is a deuterated form of a chiral molecule that is used in biochemical research as a reference standard in mass spectrometry. It is an essential tool in the analysis of biological samples and plays a crucial role in the development of new drugs and in understanding the metabolic pathways of living organisms.

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