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Merck
CN

H1377

4-Hydroxy-3-methoxyphenylglycol hemipiperazinium salt

Cerebral norepinephrine metabolite

Synonym(s):

3-Methoxy-4-hydroxy-phenylglycol piperazine, MHPG piperazine, MOPEG, MOPEG piperazine

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About This Item

Empirical Formula (Hill Notation):
C9H12O4 · 0.5C4H10N2
CAS Number:
Molecular Weight:
227.26
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
266-689-7
MDL number:
Beilstein/REAXYS Number:
7360817
Quality level:
Technical Service
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Product Name

4-Hydroxy-3-methoxyphenylglycol hemipiperazinium salt,

storage temp.

2-8°C

Quality Level

SMILES string

C1CNCCN1.COc2cc(ccc2O)C(O)CO.COc3cc(ccc3O)C(O)CO

InChI

1S/2C9H12O4.C4H10N2/c2*1-13-9-4-6(8(12)5-10)2-3-7(9)11;1-2-6-4-3-5-1/h2*2-4,8,10-12H,5H2,1H3;5-6H,1-4H2

InChI key

KCECBJRHWSOTMR-UHFFFAOYSA-N

Biochem/physiol Actions

Cerebral norepinephrine metabolite.

Features and Benefits

This compound is featured on the Dopamine and Norepinephrine Metabolism page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.


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pictograms

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signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves



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M L Laorden et al.
Life sciences, 66(9), 803-815 (2000-03-04)
Previous report from our laboratory showed that morphine produces a stimulatory effect of hypothalamic noradrenaline (NA) turnover concurrently with enhanced pituitary-adrenal response after its acute injection and during withdrawal. In the present work we have studied the effects of acute
Y Wada et al.
Japanese journal of pharmacology, 78(2), 237-240 (1998-11-26)
To study the circadian rhythm of the monoamine and metabolite contents, cerebrospinal fluid was taken from the cisterna magna through a polyethylene catheter tube every 4 hr in the conscious rat. Norepinephrine and 3-methoxy-4-hydroxy-phenylglycol were found to describe a rhythm
J M Duine et al.
Journal of chromatography. B, Biomedical sciences and applications, 716(1-2), 350-353 (1998-11-21)
A reversed-phase chromatographic method with electrochemical detection was developed for the simultaneous determination of 2,3- and 2,5-dihydroxybenzoates, indicators of in vivo hydroxyl free radical formation, monoamines (NE, DA, 5-HT) and their metabolites (MHPG, DOPAC, HVA, 3MT, 5-HIAA). Linearity was observed



Global Trade Item Number

SKUGTIN
H1377-50MG04061832082356
H1377-5MG04061832082363
H1377-25MG04061833665121
H1377-100MG04061832091150