Current location:Home > Pharmaceutical
Product
Chinese factory supply Tyramine hydrochloride 60-19-5 in stock with high standard
- Molecular Formula:C8H12ClNO
- Molecular Weight:173.642
- Appearance/Colour:off-white to light yellow powder
- Vapor Pressure:0.000123mmHg at 25°C
- Melting Point:253-255 °C(lit.)
- Refractive Index:1.577
- Boiling Point:325.2 °C at 760 mmHg
- Flash Point:119.2 °C
- PSA:46.25000
- Density:1.103 g/cm3
- LogP:2.39570
Tyramine hydrochloride(Cas 60-19-5) Usage
|
Biochem/physiol Actions |
Tyramine is a biogenic amine and a neuromodulator localized to the nervous system. Tyrosine decarboxylase catalysis the formation of tyramine from tyrosine. Tyramine is found to be associated with a number of psychiatric disorders. Tyramine ingestion depletes serotonin, epinephrine and norepinephrine reserves. This results in elevated biological events such as cardiovascular function, blood pressure, glucose production and overall metabolism. It also causes depression, migraine and insomnia. Tyramine is present is several food sources. The process of food fermentation and spoilage increases its tyramine content. |
|
Synthesis |
Tyramine [2-(p-hydroxyphenyl) ethylamine], a significant metabolite of tyrosine, enzymatic synthesis of tyramine was established by two-step biocatalytic reaction. Firstly, l-tyrosine was prepared from raw pyruvate fermentation broth under the catalysis of TPL. Pyruvate fermentation broth was simply centrifuged, and then the supernatant was diluted and used as substrate to produce l-tyrosine. Secondly, l-tyrosine was collected as starting material to synthesize tyramine by immobilized TDC cells from Lactobacillus brevis. Pyridoxal phosphate was the common coenzyme for these two enzymes. |
|
Purification Methods |
Crystallise the hydrochloride from EtOH by addition of diethyl ether, or from conc HCl. [Beilstein 3 II 355.] |
|
Application |
Tyramine hydrochloride (T-HCl) is a kind of fluorogenic substrate of peroxidase. It is a naturally occurring monoamine derived from tyrosine. Tyramine Hydrochloride has been used:coinfused with adenosine in control subjects and patients in order to reduce leg blood flow by 50% without affecting arterial blood pressure.labelled with fluorescence dyes (Atto 488 and Atto 655) to serve as a substrate for peroxidase in immunofluorescence analysis.used in dimethylformamide, labelled with 5-(and-6)carboxyfluorescein, succinimidyl ester/biotin to serve as a substrate for peroxidase in tyramide signal amplification.Neurotransmitter. |
InChI:InChI=1/C8H11NO/c9-6-5-7-1-3-8(10)4-2-7/h1-4,10H,5-6,9H2
60-19-5 Relevant articles
Catalytic Strategy for Regioselective Arylethylamine Synthesis
Boyington, Allyson J.,Seath, Ciaran P.,Zearfoss, Avery M.,Xu, Zihao,Jui, Nathan T.
supporting information, p. 4147 - 4153 (2019/03/07)
A mild, modular, and practical catalytic...
Synthetic method for tyramine hydrochloride
-
Paragraph 0030; 0033; 0034, (2017/01/31)
The invention discloses a synthetic meth...
Rapid Conventional and Microwave-Assisted Decarboxylation of L-Histidine and Other Amino Acids via Organocatalysis with R-Carvone under Superheated Conditions
Jackson, Douglas M.,Ashley, Robert L.,Brownfield, Callan B.,Morrison, Daniel R.,Morrison, Richard W.
, p. 2691 - 2700 (2015/12/18)
This article reports a new methodology t...
METHOD FOR DECARBOXYLATION OF AMINO ACIDS VIA IMINE FORMATION
-
Page/Page column 0045; 0056; 0066; 0067, (2014/09/30)
The present application provides methods...
60-19-5 Process route
-
-
60-18-4,18875-48-4,25619-78-7,30704-25-7
L-tyrosine
-
-
60-19-5
tyramine hydrochloride
| Conditions | Yield |
|---|---|
|
L-tyrosine;
With
(R)-Carvone;
In
propan-1-ol;
at 190 ℃;
for 0.666667h;
under 11251.1 Torr;
Sealed tube;
With
hydrogenchloride;
In
propan-1-ol; water;
at 190 ℃;
for 0.0833333h;
|
67% |
|
Multi-step reaction with 2 steps
1: propan-1-ol / 20 - 190 °C / Green chemistry
2: hydrogenchloride / propan-1-ol / 0.67 h / 190 °C / Green chemistry
With
hydrogenchloride;
In
propan-1-ol;
|
-
-
p-hydroxyphenyl-α-isonitrosoacetophenone
-
-
60-19-5
tyramine hydrochloride
| Conditions | Yield |
|---|---|
|
With
hydrogenchloride; hydrogen;
palladium;
In
indication of hydrogen; water;
|
85% |
60-19-5 Upstream products
-
2982-55-0
1-benzyloxy-4-(2-nitroethenyl)benzene
-
66648-43-9
(E)-N-feruloyltyramine
-
2982-54-9
2-[4-(benzyloxy)phenyl]ethylamine hydrochloride
-
148715-54-2
4-<2(E)-(4,5-diphenyl-2-oxo-4-oxazolin-3-yl)ethenyl>phenol
60-19-5 Downstream products
-
98489-01-1
2-(3-bromo-4-hydroxyphenyl)ethylamine
-
1202-66-0
N-acetyltyramine
-
70833-92-0
14-hydroxy-3β-(O4-{O4-[(7S)-4-(4-hydroxy-phenethyl)-2c-methyl-[1,4]oxazepan-7r-yl]-β-D-ribo-2,6-dideoxy-hexopyranosyl}-β-D-ribo-2,6-dideoxy-hexopyranosyloxy)-(5β,14β)-card-20(22)-enolide
-
63544-70-7
12β,14-dihydroxy-3β-(O4-{O4-[(7S)-4-(4-hydroxy-phenethyl)-2c-methyl-[1,4]oxazepan-7r-yl]-β-D-ribo-2,6-dideoxy-hexopyranosyl}-β-D-ribo-2,6-dideoxy-hexopyranosyloxy)-(5β,14β)-card-20(22)-enolide
