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Merck

T3754

Sigma-Aldrich

L-Tirosina

≥98% (HPLC)

Sinónimos:

3-(4-Hidroxifenil)-L-alanina, Ácido (S)-2-Amino-3-(4-hidroxifenil)propiónico

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About This Item

Fórmula lineal:
4-(HO)C6H4CH2CH(NH2)CO2H
Número de CAS:
Peso molecular:
181.19
Beilstein/REAXYS Number:
392441
EC Number:
MDL number:
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.26

product name

L-Tirosina, reagent grade, ≥98% (HPLC)

grade

reagent grade

Quality Level

assay

≥98% (HPLC)

form

powder

color

white to off-white

mp

>300 °C (dec.) (lit.)

solubility

1 M HCl: soluble 50 mg/mL

application(s)

detection

SMILES string

N[C@@H](Cc1ccc(O)cc1)C(O)=O

InChI

1S/C9H11NO3/c10-8(9(12)13)5-6-1-3-7(11)4-2-6/h1-4,8,11H,5,10H2,(H,12,13)/t8-/m0/s1

InChI key

OUYCCCASQSFEME-QMMMGPOBSA-N

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Categorías relacionadas

Application

L-Tyrosine has been used to prepare tyrosine solution for tyrosinase assay. It has also been used to assay pepsin activity.

Biochem/physiol Actions

L-Tyrosine is a non-essential amino acid with a polar side chain. It is utilized by cells to synthesize proteins that have a role in signal transduction. L-Tyrosine is a proteogenic amino acid that acts as a receiver of phosphate groups that are transferred by kinases.

Other Notes

Aminoácido precursor de la dopamina y otras catecolaminas

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Protocolos

Proteinase K activity measured via spectrophotometry using hemoglobin substrate, crucial for enzyme characterization.

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