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Supelco

Tyramin

analytical standard

Synonym(e):

2-(4-Hydroxyphenyl)-ethylamin, 4-(2-Aminoethyl)-phenol

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About This Item

Lineare Formel:
HOC6H4CH2CH2NH2
CAS-Nummer:
51-67-2
Molekulargewicht:
137.18
Beilstein:
1099914
EG-Nummer:
200-115-8
MDL-Nummer:
MFCD00008193
UNSPSC-Code:
85151701
PubChem Substanz-ID:
329768808
NACRES:
NA.24

Qualität

analytical standard

Qualitätsniveau

100

Assay

≥98.5% (GC)
98.0-102.0% (wt., NT)

Haltbarkeit

limited shelf life, expiry date on the label

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

bp

175-181 °C/8 mmHg (lit.)

mp (Schmelzpunkt)

160-162 °C (lit.)

Eignung

conforms to structure for Infrared spectrum

Anwendung(en)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Format

neat

Lagertemp.

2-8°C

SMILES String

NCCc1ccc(O)cc1

InChI

1S/C8H11NO/c9-6-5-7-1-3-8(10)4-2-7/h1-4,10H,5-6,9H2

InChIKey

DZGWFCGJZKJUFP-UHFFFAOYSA-N

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Verwandte Kategorien

Anwendung

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Biochem./physiol. Wirkung

Kann in catecholaminerge Endungen eintreten und als falscher Transmitter freigegeben werden.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Choose from one of the most recent versions:

Analysenzertifikate (COA)

Lot/Batch Number
BCCM4984
BCCJ9693
BCCG2965
BCCD2623
BCBZ8695

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(±)-Octopamin -hydrochlorid analytical standard

Supelco

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(±)-Octopamin -hydrochlorid

N-Acetyltyramine ≥95% (LC/MS-ELSD)

Sigma-Aldrich

SMB00019

N-Acetyltyramine

Cadaverin purum, ≥97.0% (GC)

Sigma-Aldrich

33211

Cadaverin

Parthenolid phyproof® Reference Substance

PHL89255

Parthenolid

Cadaverin 95%

Sigma-Aldrich

D22606

Cadaverin

Histamin ≥97.0%

Sigma-Aldrich

H7125

Histamin

Thomas Roeder et al.
Archives of insect biochemistry and physiology, 54(1), 1-13 (2003-08-28)
The phenolamines tyramine and octopamine are decarboxylation products of the amino acid tyrosine. Although tyramine is the biological precursor of octopamine, both compounds are independent neurotransmitters, acting through various G-protein coupled receptors. Especially, octopamine modulates a plethora of behaviors, peripheral
Thomas Roeder
Annual review of entomology, 50, 447-477 (2004-09-10)
Octopamine (OA) and tyramine (TA) are the invertebrate counterparts of the vertebrate adrenergic transmitters. They are decarboxylation products of the amino acid tyrosine, with TA as the biological precursor of OA. Nevertheless, both compounds are independent neurotransmitters that act through
R J Kohlenberg
Headache, 22(1), 30-34 (1982-01-01)
The hypothesis that oral tyramine causes migraine headache in certain patients was proposed by Hanington in 1967. In all, there are 11 published reports that experimentally test the hypothesis. Six of these studies provide support for the hypothesis whereas the
M G Bianchetti et al.
Klinische Wochenschrift, 60(9), 465-470 (1982-05-03)
Responses of blood pressure and plasma catecholamines to intravenous injection of tyramine at increasing dosage (30, 45, and 60 microgram/kg, respectively) were evaluated in 25 normal subjects and 20 patients with mild essential hypertension. Basal plasma norepinephrine and epinephrine concentrations
Moussa B H Youdim et al.
Neurotoxicology, 25(1-2), 243-250 (2003-12-31)
The major side effect with the use of first generation of non selective monoamine oxidase (MAO) inhibitors as neuropsychiatric drugs was what became known as the "cheese reaction". Namely, potentiation of sympathomimetic activity of ingested tyramine present in cheese and
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