L-M-m-tyrosine, 98%

L-M-m-tyrosine,98% structural formula

Structural formula

Business number 05Z2
Molecular formula C9H11NO3
Molecular weight 181.19
label

L-M-tyrosine,98%,

L-M-tyrosine,

L-Metatyrosine,

3-HYDROXY-L-PHENYLALANINE,

H-S-META-TYR-OH,

H-M-TYR-OH,

L-3-HYDROXY-PHENYLALANINE,

L-M-TYR,

L-M-TYROSINE,

L-META-TYROSINE,

META-TYROSINE,

Phenylalanine analogs alpha and other aromatic amino acids,

Amino acids and derivatives

Numbering system

CAS number:587-33-7

MDL number:MFCD00063059

EINECS number:None

RTECS number:None

BRN number:None

PubChem ID:None

Physical property data

1. Physical property data


1. Properties: colorless or light yellow transparent liquid.


2. Melting point17-18,


3. Boiling point213-214,550.133kPa),


4. Relative density1.2410(20/4 ) ,


5.Refractive index1.5650.


6. Soluble in ethanol, ether, benzene and acetone, slightly soluble in water.

Toxicological data

None yet

Ecological data

None yet

Molecular structure data


5. Molecular property data:


1 Molar refractive index:47.37


2 Molar volume (m3/mol):135.8


3 Isotonic specific volume (90.2K):386.8


4 Surface tension (dyne/cm): 65.7


5, Polarizability (10-24cm3 ):18.78

Compute chemical data

1. Reference value for hydrophobic parameter calculation (XlogP): None

2. Number of hydrogen bond donors: 3

3. Number of hydrogen bond acceptors: 4

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: 9

6. Topological molecule polar surface area 83.6

7. Number of heavy atoms: 13

8. Surface charge: 0

9. Complexity: 184

10. Number of isotope atoms: 0

11. Determine the number of atomic stereocenters: 1

12. Uncertain number of atomic stereocenters: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Properties and stability

1. Basic properties


In living organisms it May be a precursor or intermediate of catecholamines. Para-hydroxylation of phenylalanine in vivo by meta-hydroxylase(For example, meta-hydroxylation is carried out before the formation of dopa, followed by decarboxylation to generate dopamine,dopamine). L-m-Tyrosine can penetrate the blood-brain barrier and decarboxylate into tyrosinem-Tyramine, which has the effect of stimulating dopamine receptors.

Storage method

None yet

Synthesis method

2. Introduction to production methods


It is available with Euphorbia Family, Euphorbia(Euphorbia myrsztiites L.), it can also be obtained by semi-synthetic method.

Purpose

3. Purpose


Currently it is mainly used in biochemical reagents.

This article is from the Internet, does not represent the position of Toluene diisocyanate reproduced please specify the source.https://www.chemicalchem.com/archives/29667

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