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T3629

Sigma-Aldrich

DL-m-Tyrosine

≥98% (HPLC)

Synonym(s):

(±)-2-Amino-3-(3-hydroxyphenyl)propionic acid, 3-(3-Hydroxyphenyl)-DL-alanine

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About This Item

Linear Formula:
HOC6H4CH2CH(NH2)CO2H
CAS Number:
775-06-4
Molecular Weight:
181.19
Beilstein:
2416853
EC Number:
212-270-9
MDL number:
MFCD00002597
UNSPSC Code:
12352209
PubChem Substance ID:
24900153
NACRES:
NA.26

product name

DL-m-Tyrosine, crystalline

Assay

≥98% (HPLC)

Quality Level

200

form

crystalline

color

off-white to yellow

mp

280-285 °C (dec.) (lit.)

solubility

1 M HCl: soluble

application(s)

detection

SMILES string

NC(Cc1cccc(O)c1)C(O)=O

InChI

1S/C9H11NO3/c10-8(9(12)13)5-6-2-1-3-7(11)4-6/h1-4,8,11H,5,10H2,(H,12,13)

InChI key

JZKXXXDKRQWDET-UHFFFAOYSA-N

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Related Categories

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

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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Catecholamines and dihydroxyphenylalanine in metamorphosing larvae of the nudibranch Phestilla sibogae Bergh (Gastropoda: Opisthobranchia).
Pires A, Coon SL, Hadfield MG.
J. Comp. Physiol., 181, 187-194 (1997)
A Pappa-Louisi et al.
Methods in molecular biology (Clifton, N.J.), 828, 101-114 (2011-11-30)
The combined use of a dual-UV detector as well as a fluorimetric and a multielectrode electrochemical detector (equipped with a dual electrode, consisting of a conventional size 3 mm diameter glassy carbon electrode (GCE) and of a pair of 30
P Manini et al.
The Journal of organic chemistry, 66(15), 5048-5053 (2001-07-21)
In 0.1 M phosphate buffer at pH 7.4 and 37 degrees C, the tyrosine metabolite L-3,4-dihydroxyphenylalanine (L-DOPA) reacts smoothly with D-glucose to afford, besides diastereoisomeric tetrahydroisoquinolines 1 and 2 by Pictet-Spengler condensation, a main product shown to be the unexpected
Philip H Elsinga et al.
Current medicinal chemistry, 13(18), 2139-2153 (2006-08-22)
The dopaminergic system plays a major role in neurological and psychiatric disorders such as Parkinson's disease, Huntington's disease, tardive dyskinea and schizophrenia. Knowledge on altered dopamine synthesis, receptor densities and status are important for understanding the mechanisms underlying the pathogenesis
Tengfang Huang et al.
Phytochemistry, 75, 60-66 (2011-12-24)
m-Tyrosine is a non-protein amino acid that is structurally similar to the common protein amino acids p-tyrosine and phenylalanine. Copious amounts of m-tyrosine can be found in root exudates of the fine fescue cultivar, Festuca rubra L. ssp. commutata (Chewings
View All Related Papers

Chromatograms

application for HPLC

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