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Merck
CN

615609

Indole-2,4,5,6,7-d5-3-acetic-2,2-d2 acid

97 atom % D

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About This Item

Empirical Formula (Hill Notation):
C10D7H2NO2
Molecular Weight:
182.23
UNSPSC Code:
12352005
PubChem Substance ID:
329759555
MDL number:
MFCD04118278

Key Documents

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Product Name

Indole-2,4,5,6,7-d5-3-acetic-2,2-d2 acid, 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

Related Categories

Application

- Acid-catalyzed reaction mechanism studies
- Chemical synthesis of labeled compounds
- Advanced materials research and development
- Analytical method development

Features and Benefits

Features
  • 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.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
IG0298

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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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