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Tyramine hydrochloride | 60-19-5
| Catelog Number | F10-0133 |
| Category | ATTO |
| Molecular Formula | C8H11NO·HCl |
| Molecular Weight | 173.64 |
| Catalog Number | Size | Price | Quantity |
|---|---|---|---|
| F10-0133 | -- | $-- |
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Product Introduction
A naturally occurring derivative of tyrosine. A catecholamine releasing agent that promotes blood pressure elevation.
Chemical Information |
|
|---|---|
| Synonyms | 4-(2-Aminoethyl)phenol hydrochloride; 4-Hydroxyphenethylamine hydrochloride |
| Purity | 98.0% |
| IUPAC Name | 4-(2-aminoethyl)phenol;hydrochloride |
| Canonical SMILES | C1=CC(=CC=C1CCN)O.Cl |
| InChI | InChI=1S/C8H11NO.ClH/c9-6-5-7-1-3-8(10)4-2-7;/h1-4,10H,5-6,9H2;1H |
| InChI Key | RNISDHSYKZAWOK-UHFFFAOYSA-N |
| Melting Point | 271-274 °C (lit.) |
| MDL Number | MFCD00012901 |
| NACRES | NA.77 |
Product Specification |
|
|---|---|
| Storage | Store at 2-8 °C |
| Application | Tyramine hydrochloride has been:coinfused with adenosine in control subjects and patients in order to reduce leg blood flow by 50% without affecting arterial blood pressurelabelled with fluorescence dyes (ATTO 488 and ATTO 655) to serve as a substrate for peroxidase in immunofluorescence analysisused in dimethylformamide, labelled with 5-(and-6)carboxyfluorescein, succinimidyl ester/biotin to serve as a substrate for peroxidase in tyramide signal amplification |
| Signal | Warning |
| GHS Hazard Statements | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] H319 (41.71%): Causes serious eye irritation [Warning Serious eye damage/eye irritation] H335 (100%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation] |
| Precautionary Statement Codes | P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (The corresponding statement to each P-code can be found at the GHS Classification page.) |
Computed Properties | |
|---|---|
| Hydrogen Bond Donor Count | 3 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 173.0607417 g/mol |
| Monoisotopic Mass | 173.0607417 g/mol |
| Topological Polar Surface Area | 46.2Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 87.3 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 2 |
| Compound Is Canonicalized | Yes |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 23129510 | 2013-01-01 | Molecular cloning and pharmacological characterisation of a tyramine receptor from the rice stem borer, Chilo suppressalis (Walker) | Pest management science |
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| EP-4105323-A1 | New microbial diamine oxidase derived from yarrowia lipolytica for the degradation of biogenic amines | 2021-06-15 |
| WO-2022263031-A1 | New microbial diamine oxidase derived from yarrowia lipolytica for the degradation of biogenic amines | 2021-06-15 |
| KR-20220166396-A | Fire extinguishing product to prevent fire caused by transformer insulating oil | 2021-06-09 |
| WO-2022170012-A1 | Synthesis of peg-based thiol-norbornene hydrogels with tunable hydroylitic degradation properties | 2021-02-08 |
| WO-2022099195-A1 | Ophthalmic formulation containing a dopaminergic prodrug that may be combined with one or more agents | 2020-11-09 |
Applications of Fluorescent Probes & Dyes
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