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Merck
CN

H45132

5-Hydroxy--methyltryptamine oxalate

99%

Synonym(s):

3-(2-Methylaminoethyl)indol-5-ol oxalate, N-Methylserotonin oxalate

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About This Item

Empirical Formula (Hill Notation):
C13H16N2O5
CAS Number:
Molecular Weight:
280.28
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
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Product Name

5-Hydroxy--methyltryptamine oxalate, 99%

InChI

1S/C11H14N2O.C2H2O4/c1-12-5-4-8-7-13-11-3-2-9(14)6-10(8)11;3-1(4)2(5)6/h2-3,6-7,12-14H,4-5H2,1H3;(H,3,4)(H,5,6)

SMILES string

OC(=O)C(O)=O.CNCCc1c[nH]c2ccc(O)cc12

InChI key

DYOZWAJOUTVNAF-UHFFFAOYSA-N

assay

99%

mp

161-162 °C (dec.) (lit.)

Quality Level

Application

  • reactant for preparation of 5-HT receptor agonists

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - 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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P M Lalley et al.
The Journal of physiology, 487 ( Pt 3), 653-661 (1995-09-15)
1. The effects of the 5-HT2 receptor agonist alpha-methyl-5-HT were studied on the membrane of expiratory (E2) and post-inspiratory (PI) neurones, by intracellular recordings in the caudal medulla of anaesthetized cats. 2. Ionophoresis of alpha-Me-5-HT depolarized membrane potential and increased
A R Johnston et al.
Experimental brain research, 93(2), 293-298 (1993-01-01)
The effects of 5-hydroxytryptamine (5-HT) and related compounds on the discharge rate of tonically active medial vestibular nucleus (MVN) neurones were studied in an in vitro slice preparation of the dorsal brainstem of the rat. The majority (87 of 107
D Alberghina et al.
Research in veterinary science, 90(3), 392-395 (2010-07-17)
To evaluate the changes in plasma and platelet serotonin (5-HT) as markers of the serotoninergic system in equines, 5-HT content was measured by high performance liquid chromatography (HPLC) in deproteinized plasma obtained from peripheral blood samples of 12 clinically healthy
C R Ashby et al.
Synapse (New York, N.Y.), 17(3), 173-181 (1994-07-01)
In this study, we examined the interaction of 5-HT1A and 5-HT2A receptors in the rat medial prefrontal cortex (mPFc) using the techniques of extracellular single unit recording and microiontophoresis. The iontophoresis of the selective 5-HT1A receptor agonist (+-)-8-hydroxy-2-(di-n-propylamino) tetralin (8-OHDPAT)
Sharla L Powell et al.
Journal of agricultural and food chemistry, 56(24), 11718-11726 (2008-12-04)
Cimicifuga racemosa (L.) Nutt. (syn. Actaea racemosa L., black cohosh) is used to relieve menopausal hot flashes, although clinical studies have provided conflicting data, and the active constituent(s) and mechanism(s) of action remain unknown. Because serotonergic receptors and transporters are

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