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209848
α-(Methylaminomethyl)benzyl alcohol
99%
Synonim(y):
Halostachine
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About This Item
Polecane produkty
Próba
99%
Postać
solid
mp
74-76 °C (lit.)
grupa funkcyjna
amine
hydroxyl
phenyl
ciąg SMILES
CNCC(O)c1ccccc1
InChI
1S/C9H13NO/c1-10-7-9(11)8-5-3-2-4-6-8/h2-6,9-11H,7H2,1H3
Klucz InChI
ZCTYHONEGJTYQV-UHFFFAOYSA-N
Opis ogólny
α-(Methylaminomethyl)benzyl alcohol is a potential substrate for studies involving phenylethanolamine-N-methyltransferase.
Zastosowanie
α-(Methylaminomethyl)benzyl alcohol was used in the synthesis of 1,4-disubstituted-2,3,4,5-tetrahydro-1H-3-benzazepines. It was also used as internal standard during determination of pseudoephedrine and phenylpropanolamine urine concentrations by HPLC.
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Hasło ostrzegawcze
Warning
Zwroty wskazujące rodzaj zagrożenia
Zwroty wskazujące środki ostrożności
Klasyfikacja zagrożeń
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
Kod klasy składowania
11 - Combustible Solids
Klasa zagrożenia wodnego (WGK)
WGK 3
Temperatura zapłonu (°F)
Not applicable
Temperatura zapłonu (°C)
Not applicable
Środki ochrony indywidualnej
dust mask type N95 (US), Eyeshields, Gloves
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Organic letters, 2(25), 4099-4102 (2000-12-12)
[structure] Two general routes to 1,4-disubstituted-2,3,4, 5-tetrahydro-1H-3-benzazepines are described. Both routes utilize an appropriately functionalized phenethylamino alcohol as the penultimate intermediate: the first route makes use of the reductive amination of a benzyl alkyl ketone with alpha-(aminomethyl)benzyl alcohol, while the
British journal of clinical pharmacology, 57(1), 62-67 (2003-12-18)
To study the elimination of ephedrines with reference to the International Olympic Committee (IOC) doping control cut-off levels, following multiple dosing of over-the-counter decongestant preparations. A double-blind study was performed in which 16 healthy male volunteers were administered either pseudoephedrine
Progress in neuro-psychopharmacology & biological psychiatry, 8(3), 385-395 (1984-01-01)
The radiotracers, C-14-N-methylphenylethylamine (MPEA) and N-methylphenylethanolamine (MPEOA) both rapidly entered mouse brain after their intravenous injection and were metabolized by brain monoamine oxidase (MAO) to C-14-methylamine and corresponding aldehydes. The labelled metabolite was trapped in the brain. Measurement of radioactivity
The vasoactive potential of halostachine, an alkaloid of tall fescue (Festuca arundinaceae, Schreb) in cattle.
Veterinary and human toxicology, 25(6), 408-411 (1983-12-01)
The Journal of pharmacology and experimental therapeutics, 217(2), 379-385 (1981-05-01)
Single i.v. doses of the endogenous trace amine phenylethanolamine (PEOH) and its N-methyl homolog (NMPEOH) were administered to separate groups of five dogs. The dose- and time-related effects of these compounds were measured on pupillary diameter, heart rate and body
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