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Thermo Scientific Chemicals L-Tyrosine, +99%

Catalog Number AC140640010
Click to view available options
Quantity:
5 g
100 g
1 kg
Packaging:
Glass Bottle
Plastic Bottle
60-18-4
C9H11NO3
181.19
MFCD00002606
OUYCCCASQSFEME-SVGMAFHSNA-N
l-tyrosine, tyrosine, s-tyrosine, p-tyrosine, h-tyr-oh, l-p-tyrosine, 2s-2-amino-3-4-hydroxyphenyl propanoic acid, 4-hydroxy-l-phenylalanine, l---tyrosine, tyrosine, l
6057
CHEBI:17895
(2S)-2-amino-3-(4-hydroxyphenyl)propanoic acid
N[C@@H](CC1=CC=C(O)C=C1)C(O)=O
60-18-4
C9H11NO3
181.19
MFCD00002606
OUYCCCASQSFEME-SVGMAFHSNA-N
l-tyrosine, tyrosine, s-tyrosine, p-tyrosine, h-tyr-oh, l-p-tyrosine, 2s-2-amino-3-4-hydroxyphenyl propanoic acid, 4-hydroxy-l-phenylalanine, l---tyrosine, tyrosine, l
6057
CHEBI:17895
(2S)-2-amino-3-(4-hydroxyphenyl)propanoic acid
N[C@@H](CC1=CC=C(O)C=C1)C(O)=O

L-Tyrosine, CAS # 60-18-4, is an aromatic non-essential amino acid that is considered a fundamental metabolite, involved in protein synthesis and photosynthesis.

This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

General description

• L-Tyrosine is the levorotatory isomer of the aromatic amino acid tyrosine, synthesized in vivo from L-phenylalanine
• It is available as a crystalline, off-white powder, stable at room temperature, and soluble in hydrochloric acid

Applications

• In vivo L-tyrosine is involved in protein synthesis and is a precursor to alkaloids such as morphine, neurotransmitters, epinephrine, p-coumaric acid, thyroxine, pigment melanin and catecholamines.
• Used as a supplement, L-tyrosine has been shown to increase levels of the neurotransmitters, dopamine, adrenaline, and norepinephrine in the brain
• It is considered an essential dietary supplement for phenylketonuria patients who lack the enzyme phenylalanine hydroxylase, and hence cannot convert phenylalanine into tyrosine
• L-tyrosine plays a vital role as an electron-carrier in the process of photosynthesis
• Due to its role in the synthesis of catecholamines, L-tyrosine is also used in research to study its impact on stress

TRUSTED_SUSTAINABILITY
Color White
Assay Percent Range 99+%
Infrared Spectrum Authentic
Linear Formula 4-(HO)C6H4CH2CH(NH2)CO2H
Beilstein 14, 605
Loss on Drying 0.5% max. (1 g, 105°C)
Merck Index 15, 10020
Packaging Plastic Bottle
Specific Rotation -9.8° to -12.3° (20°C, 589nm) (c=5, 1N HCl)
Formula Weight 181.19
Percent Purity ≥99.0% (on dried substance)
Sulfated Ash 0.1% max.
Specific Rotation Condition − 11.05 (20.00°C c=5,dilHCL/H2O 50/50)
Quantity 1 kg
Physical Form Crystalline Powder
Chemical Name or Material L-Tyrosine
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Hazard Statement GHS H Statement:
May cause respiratory irritation.
Causes serious eye irritation.
Causes skin irritation.
Precautionary Statement GHS P Statement:
Avoid breathing dust/fume/gas/mist/vapors/spray.
IF ON SKIN: Wash with plenty of soap and water.
Wear protective gloves/protective clothing/eye protection/face protection.
IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.

WARNING: The information provided on this web site was developed in compliance with European Union (EU) regulations and is correct to the best of our knowledge, information and belief at the date of its publication. The information given is designed only as a guide for safe handling and use. It is not to be considered as either a warranty or quality specification.

RUO – Research Use Only

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