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Sigma-Aldrich

L-Tryptophan-(indole-d5)

97 atom % D

Synonym(s):

(S)-2-Amino-3-(3-indoyl-d5)propionic acid, L-α-Amino-(3-indole-d5)propionic acid, Deuterated Trp, Deuterated tryptophan, Trp-d5

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About This Item

Empirical Formula (Hill Notation):
C11D5H7N2O2
CAS Number:
62595-11-3
Molecular Weight:
209.26
MDL number:
MFCD00144688
UNSPSC Code:
12352209
PubChem Substance ID:
24881953
NACRES:
NA.12

isotopic purity

97 atom % D

form

solid

optical activity

[α]20/D -30.5°, c = 1 in H2O

mp

280-285 °C (dec.) (lit.)

mass shift

M+5

SMILES string

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

InChI

1S/C11H12N2O2/c12-9(11(14)15)5-7-6-13-10-4-2-1-3-8(7)10/h1-4,6,9,13H,5,12H2,(H,14,15)/t9-/m0/s1/i1D,2D,3D,4D,6D

InChI key

QIVBCDIJIAJPQS-HLTLGYGQSA-N

General description

L-Tryptophan-(indole-d5) is an isotopically labeled analogue of L-Tryptophan.

Application

L-Tryptophan-(indole-d5) is used
• in biophysical study for neutron scattering.
• as an internal standard for the investigation of anti-inflammatory activity of low molecular weight fractions.
• in structural elucidation of micronutrients and nutraceutical components presence in food stuffs using LC-MS/MS.

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 Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

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Gregory W Thomas et al.
Journal of immunoassay & immunochemistry, 37(1), 55-67 (2015-05-12)
The innate immune system is increasingly being recognized as a critical component in osteoarthritis (OA) pathophysiology. An ex vivo immunoassay utilizing human peripheral blood mononuclear cells (PBMC) was developed in order to assess the OA anti-inflammatory properties of the low
Valerie Laux et al.
European biophysics journal : EBJ, 37(6), 815-822 (2008-02-16)
We describe methods that have been developed within the ILL-EMBL Deuteration Laboratory for the production of maltose binding protein (MBP) that has been selectively labelled either with deuterated tryptophan or deuterated methionine (single labelling), or both (double labelling). MBP is
Sara Vitalini et al.
Molecules (Basel, Switzerland), 25(2) (2020-01-17)
Food plants contain hundreds of bioactive phytochemicals arising from different secondary metabolic pathways. Among these, the metabolic route of the amino acid Tryptophan yields a large number of plant natural products with chemically and pharmacologically diverse properties. We propose the

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