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60-18-4

60-18-4 structural image
Product Name: L-Tyrosine
Formula: C9H11NO3
Synonyms: L-Tyrosine;TYR;Tyrosinase;(S)-(-)-Tyrosine;Monophenol monooxygenase
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CHEMICAL AND PHYSICAL PROPERTIES

Physical Description Solid; [Merck Index] White fine crystals and fragments; [Sigma-Aldrich MSDS]
Color/Form FINE SILKY NEEDLES
Boiling Point BOILING POINT: SUBLIMES
Melting Point 343 dec °C
Solubility 479 mg/L (at 25 °C)
LogP -2.26
LogS -2.57
Optical Rotation SPECIFIC OPTICAL ROTATION: -10.6 DEG @ 22 °C/D (C= 4 IN N HYDROCHLORIC ACID)
pH 5.66 (at isoelectric point)
Ionization Efficiency Negative
Dissociation Constants 2.06
Collision Cross Section 145.7 Ų [M+H]+ [CCS Type: DT, Method: single field calibrated with Agilent tune mix (Agilent)]
Other Experimental Properties OPTICALLY ACTIVE
Chemical Classes Biological Agents -> Amino Acids and Derivatives

SAFETY INFORMATION

Signal word Warning
Pictogram(s)

Exclamation Mark
Irritant
GHS07
GHS Hazard Statements H315:Skin corrosion/irritation
H319:Serious eye damage/eye irritation
H335:Specific target organ toxicity, single exposure;Respiratory tract irritation
Precautionary Statement Codes P261:Avoid breathing dust/fume/gas/mist/vapours/spray.
P304+P340:IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P405:Store locked up.

COMPUTED DESCRIPTORS

Molecular Weight 181.19 g/mol
XLogP3 -2.3
Hydrogen Bond Donor Count 3
Hydrogen Bond Acceptor Count 4
Rotatable Bond Count 3
Exact Mass 181.07389321 g/mol
Monoisotopic Mass 181.07389321 g/mol
Topological Polar Surface Area 83.6 Ų
Heavy Atom Count 13
Formal Charge 0
Complexity 176
Isotope Atom Count 0
Defined Atom Stereocenter Count 1
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
Covalently-Bonded Unit Count 1
Compound Is Canonicalized Yes

PRODUCT INTRODUCTION

description

L-Tyrosine, also known simply as tyrosine, is an amino acid. It is an optically active form of tyrosine having L-configuration. It falls under the category of nonessential amino acids since the body can synthesize it from another amino acid, phenylalanine. Acting as the precursor for catecholamines, alterations in L-tyrosine availability to the brain can impact dopamine and norepinephrine synthesis in both experimental animals and likely in humans. In animals, stress induces increased catecholamine release, leading to their depletion, a phenomenon remedied by L-tyrosine supplementation. However, L-tyrosine does not appear to stimulate catecholamine release under basal neuronal firing rates; its effect is observed when firing rates are elevated due to stress.

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