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333786

Sigma-Aldrich

L-Dopa-(phenyl-d3)

≥98 atom % D, ≥98% (CP)

Synonym(s):

3-(3,4-Dihydroxyphenyl-2,5,6-d3)-L-alanine

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About This Item

Linear Formula:
(HO)2C6D3CH2CH(NH2)CO2H
CAS Number:
Molecular Weight:
200.21
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.12

isotopic purity

≥98 atom % D

Assay

≥98% (CP)

form

powder

optical activity

[α]27/D −11.5°, c = 5 in 1 M HCl

technique(s)

mass spectrometry (MS): suitable

mp

292 °C (dec.) (lit.)

mass shift

M+3

storage temp.

2-8°C

SMILES string

[2H]c1c([2H])c(C[C@H](N)C(O)=O)c([2H])c(O)c1O

InChI

1S/C9H11NO4/c10-6(9(13)14)3-5-1-2-7(11)8(12)4-5/h1-2,4,6,11-12H,3,10H2,(H,13,14)/t6-/m0/s1/i1D,2D,4D

InChI key

WTDRDQBEARUVNC-UOCCHMHCSA-N

Related Categories

General description

L-Dopa-(phenyl-d3) is an isotopic analogue of 3-(3,4-Dihydroxyphenyl)-L-alanine amino acid.

Application

L-Dopa-(phenyl-d3) or (3-(3,4-dihydroxyphenyl-2,5,6-d3)-L-alanine) can be used as an internal standard for the quantification of methyldopa in human plasma by LC-MS-MS based method.
L-Dopa-(phenyl-d3) can be used as an internal standard.

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.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

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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Glauber de S Araujo et al.
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L-DOPA, also known as Levodopa or L-3,4-dihydroxyphenylalanine, is a non-standard amino acid, and the gold standard drug for the treatment for Parkinson's Disease (PD). Recently, a gene encoding the enzyme that is responsible for its synthesis, as a precursor of
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Vitiligo (VIT) is caused by loss and degradation of functional epidermal melanocytes. Studies have indicated that melanocyte destruction may be associated with an imbalance between regulatory T cells (Treg cells) and effector T cells (Teff cells). The current study aimed to investigate the
Quantification of methyldopa in human plasma by high-performance liquid chromatography?electrospray tandem mass spectrometry: Application to a bioequivalence study
Oliveira CH, et al.
Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 2(768), 341-348 (2002)

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