D017
m-Tyramine hydrochloride
solid, ≥98% (HPLC)
Synonym(s):
3-Hydroxyphenethylamine hydrochloride
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C8H11NO · HCl
CAS Number:
Molecular Weight:
173.64
UNSPSC Code:
12352200
PubChem Substance ID:
EC Number:
222-396-6
MDL number:
InChI key
GTIWCKXKQGMMQZ-UHFFFAOYSA-N
InChI
1S/C8H11NO.ClH/c9-5-4-7-2-1-3-8(10)6-7;/h1-3,6,10H,4-5,9H2;1H
SMILES string
Cl[H].NCCc1cccc(O)c1
assay
≥98% (HPLC)
form
solid
storage condition
protect from light
color
off-white to tan
solubility
H2O: ≥10 mg/mL
Biochem/physiol Actions
Dopamine receptor agonist; biological precursor to dopamine.
Disclaimer
Photosensitive
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Storage Class
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
D A Durden et al.
Neurochemical research, 18(9), 995-1002 (1993-09-01)
Using a new ultrasensitive method the trace biogenic amines, phenylethylamine, meta-tyramine and para-tyramine have been quantitated in brain regions obtained from a single rat. Phenylethylamine concentrations in ng/g wet tissue (mean +/- std. error) were as follows: caudate 2.71 +/-
P L Walker et al.
Annals of clinical biochemistry, 25 ( Pt 3), 304-309 (1988-05-01)
A simple, reliable method for the analysis of urinary meta- and para-tyramine has been developed. Sample purification was achieved by a weak anion-exchange column, followed by extraction into ethyl acetate at pH 10.2. The heptafluorobutyryl derivative was measured by packed
S C Yeung et al.
General pharmacology, 16(5), 517-519 (1985-01-01)
The concentration of homovanillic acid and p-tyramine in the female corpus striatum were increased after ovariectomy. The increases were reversed by chronic administration of estradiol benzoate and potentiated by progesterone. It is proposed that these changes are the consequence of
H Wayment et al.
Journal of neurochemistry, 70(5), 1941-1949 (1998-05-08)
Experiments were conducted to determine how (-)-cocaine and S(+)-amphetamine binding sites relate to each other and to the catechol substrate site on the striatal dopamine transporter (sDAT). In controls, m-tyramine and S(+)-amphetamine caused release of dopamine from intracellular stores at
D L Murphy et al.
Journal of neural transmission. Supplementum, 52, 39-48 (1998-06-13)
Marked, dose-dependent elevations in the urinary excretion of phenylethylamine, para-tyramine, and meta-tyramine were observed in depressed patients treated for three or more weeks with 10, 30, or 60 mg/day of the partially-selective inhibitor of MAO-B, selegiline (l-deprenyl). In comparative studies
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service