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Merck

T2006

L-Tyrosine hydrochloride

≥98% (TLC)

Synonym(s):

3-(4-Hydroxyphenyl)-L-alanine, 3-(4-Hydroxyphenyl)-L-alanine hydrochloride

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1 G

€105.00

5 G

€397.00

10 G

€654.00

€105.00


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About This Item

Linear Formula:
HOC6H4CH2CH(NH2)CO2H·HCl
CAS Number:
Molecular Weight:
217.65
UNSPSC Code:
12352209
eCl@ss:
32160406
PubChem Substance ID:
NACRES:
NA.32
MDL number:

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Product Name

L-Tyrosine hydrochloride, ≥98% (TLC)

SMILES string

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

InChI key

JJWFIVDAMOFNPS-QRPNPIFTSA-N

InChI

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

biological source

synthetic (organic)

assay

≥98% (TLC)

form

powder

color

white to off-white

mp

239 °C (dec.) (lit.)

Quality Level

Gene Information

human ... GRIN2C(2905)
mouse ... GRIN2C(14813)
rat ... GRIN2C(24411)

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1 of 4

This Item
T375493829T2269
form

powder

form

powder

form

powder or crystals

form

powder

assay

≥98% (TLC)

assay

≥98% (HPLC)

assay

≥99.0% (NT)

assay

≥98% (HPLC)

color

white to off-white

color

white to off-white

color

white

color

white to beige

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

mp

239 °C (dec.) (lit.)

mp

>300 °C (dec.) (lit.)

mp

>300 °C (dec.) (lit.)

mp

-

biological source

synthetic (organic)

biological source

-

biological source

-

biological source

sugar beets (refined)

Biochem/physiol Actions

Tyrosine is a nonessential amino acid found in mammal, fish and birds. It participates in protein modification, such as phosphorylation, nitrosation and sulfation. It is involved in immune response regulation and prevents the generation of inflammatory cytokines and superoxide. Tyrosine serves as a precursor for epinephrine, norepinephrine, dopamine, thyroid hormones and melanin biosynthesis.[1] Tyrosine phosphorylation is associated with a number of cellular processes such as cell proliferation and migration, development of the embryo, cellular metabolism and transcription. Tyrosine phosphorylation also aids activation of the enzymatic function of a protein.[2]

Other Notes

Amino acid precursor of dopamine and other catecholamines

pictograms

Exclamation mark

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

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Resistance to Tyrosine Kinase Inhibitors, 37(1), 30-30 (2016)
Amino acids: metabolism, functions, and nutrition.
Wu G
Amino Acids, 37(1), 1-17 (2009)

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