28094-15-7 Usage
Uses
Used in Neuroscience Research:
6-HYDROXYDOPAMINE HYDROCHLORIDE is used as a neurotoxin for the creation of animal models of Parkinson's disease. It causes almost complete destruction of nigral dopaminergic neurons and their striatal terminals when injected into the substantia nigra of rats, which helps researchers study the progression and potential treatments for the disease.
Used in Cytotoxicity Studies:
6-HYDROXYDOPAMINE HYDROCHLORIDE is used as a cytotoxic agent for analyzing the cytotoxic effects on PC12 cell line, a widely used model for studying neuronal cell lines and their response to various stimuli.
Used in Neuronal Deletion Studies:
6-HYDROXYDOPAMINE HYDROCHLORIDE is used as a neurotoxin for inducing noradrenergic (NA) neuron deletion from the locus-coeruleus, a region in the brain involved in various functions such as attention, mood regulation, and stress response. This application aids in understanding the role of noradrenergic neurons in these processes and their potential involvement in various neurological disorders.
Air & Water Reactions
Hygroscopic. Water soluble.
Reactivity Profile
A weak acid. Materials in this group are generally soluble in water. The resulting solutions contain moderate concentrations of hydrogen ions and have pH's of less than 7.0. They react as acids to neutralize bases. These neutralizations generate heat, but less or far less than is generated by neutralization of inorganic acids, inorganic oxoacids, and carboxylic acid. They usually do not react as either oxidizing agents or reducing agents but such behavior is not impossible. Many of these compounds catalyze organic reactions.
Health Hazard
ACUTE/CHRONIC HAZARDS: When heated to decomposition 6-HYDROXYDOPAMINE HYDROCHLORIDE emits very toxic fumes.
Fire Hazard
Flash point data for 6-HYDROXYDOPAMINE HYDROCHLORIDE are not available. 6-HYDROXYDOPAMINE HYDROCHLORIDE is probably combustible.
Biological Activity
Selective catecholaminergic neurotoxin. Depletes brain catecholamine levels via uptake and accumulation by a transport mechanism specific to these neurons. Causes almost complete destruction of nigral dopaminergic neurons and their striatal terminals when injected into the substantia nigra of rats, producing an animal model of Parkinson's disease.
Biochem/physiol Actions
Neurotoxin that destroys catecholaminergic terminals.
Check Digit Verification of cas no
The CAS Registry Mumber 28094-15-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,9 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 28094-15:
(7*2)+(6*8)+(5*0)+(4*9)+(3*4)+(2*1)+(1*5)=117
117 % 10 = 7
So 28094-15-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO3.ClH/c9-2-1-5-3-7(11)8(12)4-6(5)10;/h3-4,10-12H,1-2,9H2;1H