Skip to Content
Merck
CN

T3629

DL-m-Tyrosine

≥98% (HPLC)

Synonym(s):

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

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

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

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

DL-m-Tyrosine, crystalline

InChI key

JZKXXXDKRQWDET-UHFFFAOYSA-N

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)

SMILES string

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

assay

≥98% (HPLC)

form

crystalline

color

off-white to yellow

mp

280-285 °C (dec.) (lit.)

solubility

1 M HCl: soluble

application(s)

detection

Quality Level

200

Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0000279188
0000279188
100M1670V
081M1778V
100M1670

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

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
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
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)
Paola Manini et al.
Carbohydrate research, 340(18), 2719-2727 (2005-10-19)
The reactions of 5-S-cysteinyldopa, L-alpha-methyldopa and DL-m-tyrosine with D-glucose were investigated at 90 degrees C in phosphate buffer at pH ranging from 5.0 to 9.0. Whereas gave mainly the double Maillard condensation product N,N'-bis(1''-deoxy-D-fructos-1''-yl)-5-S-cysteinyldopa, as an inseparable mixture of beta-D-fructopyranosyl
Jae B Park et al.
Cancer letters, 202(2), 161-171 (2003-12-04)
N-Cinnamoyltyramine, N-caffeoyltyramine, N-feruloyltyramine, and N-sinapoyltyramine were synthesized and investigated to identify the most potent compound with anti-proliferation effect on HL-60, U937 and Jurkat cells. N-Caffeoyltyramine was the most potent with GI(50)=10 microM. The treatment of the cells with N-caffeoyltyramine activated
View All Related Papers

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