335081-04-4

Basic information

• Product Name: DOPAMINE HYDROCHLORIDE
• Synonyms: 2-(3,4-DIHYDROXYPHENYL)ETHYL-1-13C-AMINE HCL;3,4-DIHYDROXYPHENYL-ETHYLAMINE HYDROCHLORIDE;3,4-DIHYDROXYPHENETHYLAMINE, HCL;4-(2-AMINOETHYL)-1-2-BENZENEDIAL HYDROCHLORIDE;4-(2-AMINOETHYL)PYROCATECHOL HYDROCHLORIDE;3-HYDROXYTYRAMINIUM CHLORIDE;HYDROXYTYRAMINE HCL;LABOTEST-BB LT00233111
• CAS NO: 335081-04-4
• Molecular Formula: C8H12ClNO2
• Molecular Weight: 189.64
• EINECS: 200-527-8
• Mol File: 335081-04-4.mol
• Article Data: 4

Chemical Properties

• Melting Point: 248-250 °C(lit.)
• Appearance: light tan/
• Storage Temp.: 0-6°C
• Solubility: alcohol: 20 mg/mL
• CAS DataBase Reference: DOPAMINE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: DOPAMINE HYDROCHLORIDE(335081-04-4)
• EPA Substance Registry System: DOPAMINE HYDROCHLORIDE(335081-04-4)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• WGK Germany: 2
• RTECS: UX1092000
• F: 8-10-23
• Hazardous Substances Data: 335081-04-4(Hazardous Substances Data)

Usage

Description

DOPAMINE HYDROCHLORIDE, also known as 2-(3,4-Dihydroxyphenyl)ethyl-1-13C-amine HCl, is a chemical compound with the CAS number 335081-04-4. It is an isotopically labeled research compound that plays a crucial role in various physiological processes and has significant applications in the medical and research fields.

Uses

Used in Pharmaceutical Industry:
DOPAMINE HYDROCHLORIDE is used as a Cardio Tonic for the treatment of various heart-related conditions. It helps in improving cardiac function and overall cardiovascular health.
Used in Research Applications:
DOPAMINE HYDROCHLORIDE is used as a research compound for studying the effects and mechanisms of dopamine in the body. Its isotopically labeled nature makes it a valuable tool for tracking and analyzing dopamine-related processes in various experimental setups.

Upstream product

• 123283-20-5 2-(3,4-dimethoxyphenyl)<1-13C>acetonitrile 
• 120-80-9 benzene-1,2-diol 

Relevant articles and documents

PROBE FOR MULTIPLE RESONANCE

PROBLEM TO BE SOLVED: To provide a precursor amino acid of a neurotransmitter capable of showing a physiologic activity or a pharmacological activity as a precursor of neurotransmitter and being detected at high selectivity in organism and to provide a probe for multiple resonance showing the physiologic activity or the pharmacological activity as the precursor of neurotransmitter and being tracked a process of metabolic reactions in organism and further being detected at high selectivity in organism. SOLUTION: There is provided a precursor amino acid of neurotransmitter represented by the formula (I), where R1 represents a hydrogen atom, an alkyl group having 1 to 4 carbon atoms which may have a substituent, an aryl group having 6 to 12 carbon atoms which may have a substituent, a heterocyclic group having 3 to 10 carbon atoms which may have a substituent or a carboxylic group, or a probe for multiple resonance containing the precursor amino acid of neurotransmitter as an active ingredient. COPYRIGHT: (C)2015,JPOandINPIT

Synthesis of Dopamines Labelled with 13C in the α- or β-Side Chain Position and Their Application to Structural Studies on Melanins by Solid-State NMR Spectroscopy

Solid-state NMR spectroscopy was applied to the analysis of melanins prepared by peroxidase-H2O2 oxidation of dopamines specifically 13C labelled in the α- or β-side chain positions.A surprisingly diverse pattern of signals indicated the presence of uncyclized dopamine and noradrenaline-derived units, in addition to indole and carbonyl carbon atoms.These structural features, coupled with the results obtained from elemental analysis of dopamine melanin samples prepared under different conditions, point to a pigment formation process more complex than previously believed. - Key Words: CP-MAS NMR Spectroscopy / Melanin / Oxidative phenolic coupling / Quinone methides / Labelled compounds, 13C / Dopamines / Enzymes