Skip to Content
MilliporeSigma
All Photos(1)

Documents

615609

Sigma-Aldrich

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

97 atom % D

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

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

isotopic purity

97 atom % D

form

solid

technique(s)

mass spectrometry (MS): suitable

mp

165-169 °C (lit.)

mass shift

M+7

SMILES string

[2H]c1[nH]c2c([2H])c([2H])c([2H])c([2H])c2c1C([2H])([2H])C(O)=O

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

InChI key

SEOVTRFCIGRIMH-PYNXLSDISA-N

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_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service