V900670
酪胺
Vetec™, reagent grade, 99%
别名:
2-(4-羟基苯基)乙胺, 4-(2-氨乙基)苯酚, 4-羟基苯乙胺
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关于此项目
线性分子式:
HOC6H4CH2CH2NH2
化学文摘社编号:
分子量:
137.18
EC Number:
200-115-8
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1099914
MDL number:
Assay:
99%
grade
reagent grade
product line
Vetec™
assay
99%
bp
175-181 °C/8 mmHg (lit.)
mp
160-162 °C (lit.)
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
InChI key
DZGWFCGJZKJUFP-UHFFFAOYSA-N
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Biochem/physiol Actions
可以进入儿茶酚胺能末梢并作为伪递质释放。
Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
存储类别
11 - Combustible Solids
wgk
WGK 3
target_organs
Respiratory system
flash_point_f
No data available
flash_point_c
No data available
Suzan El-Akaad et al.
Scientific reports, 10(1), 14479-14479 (2020-09-04)
This manuscript reports on the development of a capacitive sensor for the detection of imidacloprid (IMD) in water samples based on molecularly imprinted polymers (MIPs). MIPs used as recognition elements were synthesized via a photo-initiated emulsion polymerization. The particles were
Stephan A Chalon et al.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 28(9), 1685-1693 (2003-06-05)
Evidence suggests that compounds that increase the synaptic availability of more than one neurotransmitter have greater efficacy in the treatment of depression than single-acting drugs. Preclinical studies indicate that duloxetine acts to inhibit serotonin (5-HT) and norepinephrine (NE) transporters. The
Giris Jacob et al.
Circulation, 107(19), 2475-2479 (2003-04-23)
Despite the widespread use of tyramine as a pharmacological tool to assess the effects of norepinephrine release from sympathetic nerve terminals, its vascular effects are not adequately characterized. In particular, previous results indicate that intravenous tyramine produces little if any
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
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| V900670-5G | 04061832294933 |
| V900670-1G | 04061825859668 |
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