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333786

Sigma-Aldrich

L-Dopa-(phenyl-d3)

≥98 atom % D, ≥98% (CP)

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Synonym(s):
3-(3,4-Dihydroxyphenyl-2,5,6-d3)-L-alanine
Linear Formula:
(HO)2C6D3CH2CH(NH2)CO2H
CAS Number:
53587-29-4
Molecular Weight:
200.21
MDL number:
MFCD00075014
UNSPSC Code:
12352209
PubChem Substance ID:
24860180
NACRES:
NA.12

isotopic purity

≥98 atom % D

Quality Level

200

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
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

美国出口管控1C298产品

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.
PloS one, 7(1), e29561-e29561 (2012-01-19)
Capsule production is common among bacterial species, but relatively rare in eukaryotic microorganisms. Members of the fungal Cryptococcus genus are known to produce capsules, which are major determinants of virulence in the highly pathogenic species Cryptococcus neoformans and Cryptococcus gattii.
Dario Breitel et al.
Metabolic engineering, 65, 185-196 (2020-11-27)
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
Celso H Oliveira et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 768(2), 341-348 (2002-03-13)
A method based on LC-MS-MS is described for the determination of methyldopa in human plasma using dopa-phenyl-D3 as the internal standard. The method has a chromatographic run time of 5.5 min and was linear in the range of 20-5000 ng/ml.
Jeong-Ook Lee et al.
Journal of ginseng research, 42(3), 389-399 (2018-07-10)
The antioxidant effects of Panax ginseng have been reported in several articles; however, little is known about the antimelanogenesis effect, skin-protective effect, and cellular mechanism of Panax ginseng, especially of P. ginseng calyx. To understand how an ethanol extract of
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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