Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
In addition to treating various diseases, isotopes are used for imaging, diagnosis, and newborn screening.
Small molecule compounds labeled with stable isotopes can be used as chemical reference for chemical identification, qualitative, quantitative, detection, etc. Various types of NMR solvents can be used to study the structure, reaction mechanism and reaction kinetics of compounds.
Stable isotope labeling allows researchers to study metabolic pathways in vivo in a safe manner.
Stable isotope-labeled compounds are used as environmental pollutant standards for the detection of air, water, soil, sediment and food.
General Information |
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Catalog: BLP-007085 |
Molecular Formula: C12H20D2O11 |
Molecular Weight: 344.31 |
Chemical Structure |
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Synonyms | alpha,alpha-[1,1'-2H2]trehalose; [1-2H]Glc(a1-1a)[1-2H]Glc; alpha,alpha-trehalose-1,1'-d2; α,α-[1,1'-D2]trehalose; 1-O-α-D-[1-D]Glucopyranosyl-α-D-[1-D]glucopyranoside |
IUPAC Name | (2R,3R,4S,5S,6R)-2-deuterio-2-[(2R,3R,4S,5S,6R)-2-deuterio-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol |
Related CAS | 99-20-7 (unlabelled) |
Canonical SMILES | C(C1C(C(C(C(O1)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)O |
InChI | InChI=1S/C12H22O11/c13-1-3-5(15)7(17)9(19)11(21-3)23-12-10(20)8(18)6(16)4(2-14)22-12/h3-20H,1-2H2/t3-,4-,5-,6-,7+,8+,9-,10-,11-,12-/m1/s1/i11D,12D |
InChI Key | HDTRYLNUVZCQOY-ZYLFEKHBSA-N |
Boiling Point | 675.4±55.0 °C at 760 mmHg |
Melting Point | >189°C (dec.) |
Purity | 97% by CP; 98% atom D |
Solubility | Soluble in Water |
Appearance | White to Off-White Solid |
Storage | Store at -20°C |
α,α-Trehalose-[1,1'-d2], a deuterated variant of trehalose renowned for its protective attributes in biological systems, finds diverse applications. Here are the key applications:
Metabolic Studies: Serving as a metabolic tracer, α,α-Trehalose-[1,1'-d2] facilitates the exploration of carbohydrate metabolism across different organisms. By monitoring the assimilation and breakdown of deuterated trehalose, researchers uncover intricate metabolic pathways and fluxes. This analysis sheds light on the multifaceted roles of trehalose under varying physiological contexts, unveiling a deeper understanding of metabolic intricacies.
Proteomics Research: Within the realm of proteomics, α,α-Trehalose-[1,1'-d2] plays a critical role in stabilizing proteins and safeguarding their integrity during analytical assessments. It aids in preserving protein structure and functionality during mass spectrometry and similar techniques, ensuring precise protein detection and quantification, especially in complex biological samples. This application safeguards the fidelity of proteomic analyses, enriching the depth of biological insights.
Cryopreservation: Lending its benefits to cryopreservation practices, α,α-Trehalose-[1,1'-d2] shields cells, tissues, and biological samples from damage during freezing and thawing procedures. Its unique properties impede ice crystal formation and mitigate cellular harm, prolonging the viability and utility of preserved samples. This preservation strategy is indispensable for biobanking and enduring storage, safeguarding sample integrity and utility for future studies and applications.
Cell Stress Studies: In exploring cellular responses to stressful environments like dehydration, heat, and oxidative stress, researchers turn to α,α-Trehalose-[1,1'-d2]. Trehalose's protective properties bolster cell survival amidst adverse conditions, enabling an in-depth investigation of cellular resilience mechanisms. By deciphering these protective mechanisms, scientists pave the way for developing strategies to augment cell survival and resilience in various domains, including biotechnology and medical research.
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