ChemicalBook--->CAS DataBase List--->35424-81-8

35424-81-8

35424-81-8 Structure

35424-81-8 Structure
IdentificationBack Directory
[Name]

H-[15N]TYR-OH
[CAS]

35424-81-8
[Synonyms]

[15N]TYROSINE
H-[15N]TYR-OH
D-Trosine-15N
L-TYROSINE-15N
[15]-L-TYROSINE
L-Tyrosine-[15N1]
L-Tyrosine-UL-13C9-15N
15N Labeled L-tyrosine
H-[15N]TYR-OH USP/EP/BP
L-Tyrosine-15N
L-Tyrosine, stable isotopes
L-4-HYDROXYPHENYLALANINE-15N
L-TYROSINE-15N, 99 ATOM % 15N
L-TYROSINE-15N 98+ ATOM % 15N
3-(4-Hydroxyphenyl)-L-alanine-15N
(2S)-2-azanyl-3-(4-hydroxyphenyl)propanoic acid
(S)-2-Amino-3-(4-hydroxyphenyl)propionic acid-15N
[Molecular Formula]

C9H11NO3
[MDL Number]

MFCD00055773
[MOL File]

35424-81-8.mol
[Molecular Weight]

182.2
Chemical PropertiesBack Directory
[Melting point ]

>300 °C (dec.) (lit.)
[storage temp. ]

-15°C
[solubility ]

H2O : 11.36 mg/mL (62.36 mM; ultrasonic and warming and adjust pH to 10 with NaOH and heat to 60°C)
[form ]

Solid
[color ]

White
[optical activity]

[α]25/D -12.0°, c = 1 in 1 M HCl
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26
[WGK Germany ]

3
[HS Code ]

28459000
Hazard InformationBack Directory
[Chemical Properties]

Solid
[Uses]

L-Tyrosine-15N is labelled analogue of L-Tyrosine (T899975), one of the 22 proteinogenic amino acids that are used by cells to synthesize proteins. L-Tyrosine is biologically converted from L-phenylalanine and is in turn is converted to L-DOPA and further converted into the neurotransmitters: dopamine, norepinephrine, and epinephrine.
Spectrum DetailBack Directory
[Spectrum Detail]

H-[15N]TYR-OH(35424-81-8)Raman
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