产品名称
吲哚-2,4,5,6,7-d5-3-乙酸-2,2-d2, 97 atom % D
InChI
1S/C10H9NO2/c12-10(13)5-7-6-11-9-4-2-1-3-8(7)9/h1-4,6,11H,5H2,(H,12,13)/i1D,2D,3D,4D,5D2,6D
SMILES string
[2H]c1[nH]c2c([2H])c([2H])c([2H])c([2H])c2c1C([2H])([2H])C(O)=O
InChI key
SEOVTRFCIGRIMH-PYNXLSDISA-N
isotopic purity
97 atom % D
form
solid
technique(s)
mass spectrometry (MS): suitable
mp
165-169 °C (lit.)
mass shift
M+7
Application
- Acid-catalyzed reaction mechanism studies
- Chemical synthesis of labeled compounds
- Advanced materials research and development
- Analytical method development
- Chemical synthesis of labeled compounds
- Advanced materials research and development
- Analytical method development
Features and Benefits
Features
Benefits
- High purity of Indole-2,4,5,6,7-d5-3-acetic-2,2-d2 acid 97 atom % D ensures optimal performance.
- Versatile use in different formulations involving Indole-2,4,5,6,7-d5-3-acetic-2,2-d2 acid 97 atom % D.
- Exceptional stability and compatibility with various ingredients.
- Cost-effective solution for Indole-2,4,5,6,7-d5-3-acetic-2,2-d2 acid 97 atom % D applications.
Benefits
- Improves overall product quality and consumer satisfaction.
- Increases market competitiveness of products containing Indole-2,4,5,6,7-d5-3-acetic-2,2-d2 acid 97 atom % D.
- Reduces time to market for products utilizing Indole-2,4,5,6,7-d5-3-acetic-2,2-d2 acid 97 atom % D.
- Enhances product efficacy and reliability in formulations.
General description
Indole-2,4,5,6,7-d5-3-acetic-2,2-d2 acid 97 atom % D is a high-purity isotope product with a unique chemical profile that belongs to the class of isotopes. Produced by Sigma-Aldrich, we are committed to providing quality isotope products and a reliable supply chain. Available in industrial and pre-pack quantities.
Packaging
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Teresa Zelante et al.
Cell reports, 34(4), 108673-108673 (2021-01-28)
Indoleamine 2,3-dioxygenases (IDOs) degrade l-tryptophan to kynurenines and drive the de novo synthesis of nicotinamide adenine dinucleotide. Unsurprisingly, various invertebrates, vertebrates, and even fungi produce IDO. In mammals, IDO1 also serves as a homeostatic regulator, modulating immune response to infection
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