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H45132

Sigma-Aldrich

5-Hydroxy-Nω-methyltryptamine oxalate

99%

Synonym(s):

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

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100 MG
€165.00

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100 MG
€165.00

About This Item

Empirical Formula (Hill Notation):
C13H16N2O5
CAS Number:
1975-81-1
Molecular Weight:
280.28
MDL number:
MFCD00013159
UNSPSC Code:
12352100
PubChem Substance ID:
24895517
NACRES:
NA.22

€165.00

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Quality Level

100

Assay

99%

mp

161-162 °C (dec.) (lit.)

SMILES string

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

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)

InChI key

DYOZWAJOUTVNAF-UHFFFAOYSA-N

Related Categories

Application

  • reactant for preparation of 5-HT receptor agonists

Pictograms

Exclamation mark
GHS07

Signal Word

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBK4365
STBJ0547
STBG1582V
STBD1637V
STBC1719V

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Albrecht Pfäfflin et al.
Annals of clinical biochemistry, 46(Pt 2), 146-148 (2009-01-20)
Serotonin is frequently analysed by high-performance liquid chromatography (HPLC) with electrochemical detection. However, the accuracy of these methods may be affected by the presence of certain drugs. We describe for the first time the interference of paracetamol in therapeutic dosages
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
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)
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
Simultaneous micro-determination of serotonin and 5-hydroxyindole-3-acetic acid with 5-hydroxy-N omega-methyltryptamine, as an internal standard, in biological materials by high-performance liquid chromatography with electrochemical detection.
K Shibata et al.
Journal of chromatography, 430(2), 381-387 (1988-09-09)
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