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Merck
CN

D017

m-Tyramine hydrochloride

solid, ≥98% (HPLC)

别名:

3-Hydroxyphenethylamine hydrochloride

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关于此项目

经验公式(希尔记法):
C8H11NO · HCl
化学文摘社编号:
分子量:
173.64
UNSPSC Code:
12352200
PubChem Substance ID:
EC Number:
222-396-6
MDL number:
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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

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

存储类别

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

法规信息

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分析证书(COA)

Lot/Batch Number

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K O Schoeps et al.
Nuclear medicine and biology, 20(5), 669-678 (1993-07-01)
A method for no-carrier-added 1-11C-labelling of 3-hydroxy-, 4-hydroxy- and 3,4-dihydroxy-substituted phenethylamines is described. [11C]Dopamine, [11C]p-tyramine and [11C]m-tyramine were prepared from on-line produced [11C]nitromethane. Condensation of [11C]nitromethane with various protected and unprotected benzaldehydes was investigated. A one-pot two-step reduction of the
A A Boulton et al.
Experientia, 39(2), 130-134 (1983-02-15)
The decarboxylase inhibitor DL-alpha-monofluoromethyldopa reduces, in a dose dependent manner, the concentration of striatal p-tyramine in the mouse. Homovanillic acid is also significantly reduced. Conversely, this treatment increases the m-tyramine concentration. Administration of m-tyrosine produces large increases in m-tyramine and
A Sardar et al.
Brain research, 412(2), 370-374 (1987-06-02)
The concentrations of p-tyramine and m-tyramine have been determined in 6 brain areas from the mesolimbic system by a specific and sensitive mass spectrometric technique. p- and m-Tyramine are unevenly distributed amongst these nuclei. The highest concentrations of p-tyramine were
R S Jones et al.
Canadian journal of physiology and pharmacology, 58(2), 222-227 (1980-02-01)
p-Tyramine, applied to cortical and caudate neurones with weak iontophoretic currents (0-10 nA), did not usually cause any alteration of base-line firing rate. However, neuronal responses to dopamine (DA) during such weak applications of p-tyramine were greatly enhanced. Cortical neurone
N Chen et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 18(24), 10257-10268 (1998-12-16)
The inhibition by cocaine of inward and outward transport of dopamine (DA) at the cloned human norepinephrine transporter (hNET) and the relationship of the inhibitory patterns of cocaine to the conformational requirements of the transporter were investigated. This was done

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