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  7. Levodopa CAS#59-92-7
Levodopa CAS#59-92-7
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Levodopa CAS#59-92-7

Levodopa, also known as L-DOPA or 3,4-dihydroxy-L-phenylalanine, is a naturally occurring amino acid and a critical precursor in the biosynthesis of the neurotransmitters dopamine, norepinephrine, and epinephrine. With the molecular formula C9H11NO4, levodopa is a large, neutral amino acid that plays a significant role in the treatment of Parkinson's disease due to its ability to cross the blood-brain barrier and be converted into dopamine. Chemically, levodopa is synthesized from the precursor amino acid tyrosine through the action of the enzyme tyrosine hydroxylase. As a medication, levodopa is often formulated with a peripheral DOPA decarboxylase inhibitor to reduce its conversion to dopamine outside the brain, thereby increasing its effectiveness and reducing side effects. Levodopa is characterized by its effectiveness in alleviating the motor symptoms of Parkinson's disease, such as tremors, rigidity, and bradykinesia. It is typically administered orally and absorbed from the gastrointestinal tract, where it is then transported to the brain. <p class="last-node">In summary, levodopa is a vital pharmaceutical compound used in neurology for its role in treating Parkinson's disease by replenishing the brain's dopamine levels. Its targeted delivery and conversion to dopamine make it an essential treatment option for managing the motor symptoms associated with this condition.</p>

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Levodopa CAS#59-92-7

Levodopa, also known as L-DOPA or 3,4-dihydroxy-L-phenylalanine, is a naturally occurring amino acid and a critical precursor in the biosynthesis of the neurotransmitters dopamine, norepinephrine, and epinephrine. With the molecular formula C9H11NO4, levodopa is a large, neutral amino acid that plays a significant role in the treatment of Parkinson’s disease due to its ability to cross the blood-brain barrier and be converted into dopamine.

Chemically, levodopa is synthesized from the precursor amino acid tyrosine through the action of the enzyme tyrosine hydroxylase. As a medication, levodopa is often formulated with a peripheral DOPA decarboxylase inhibitor to reduce its conversion to dopamine outside the brain, thereby increasing its effectiveness and reducing side effects.

Levodopa is characterized by its effectiveness in alleviating the motor symptoms of Parkinson’s disease, such as tremors, rigidity, and bradykinesia. It is typically administered orally and absorbed from the gastrointestinal tract, where it is then transported to the brain.

In summary, levodopa is a vital pharmaceutical compound used in neurology for its role in treating Parkinson’s disease by replenishing the brain’s dopamine levels. Its targeted delivery and conversion to dopamine make it an essential treatment option for managing the motor symptoms associated with this condition.

Category: Petroleum Additives Tag: Petroleum Additives
  • Description

Description

Levodopa Chemical Properties
Melting point 276-278 ??C (lit.)
Boiling point 334.28??C (rough estimate)
alpha -11.7 o (c=5.3, 1N HCl)
density 1.3075 (rough estimate)
refractive index -12 ?? (C=5, 1mol/L HCl)
storage temp. 2-8??C
solubility Slightly soluble in water, practically insoluble in ethanol (96 per cent). It is freely soluble in 1 M hydrochloric acid and sparingly soluble in 0.1 M hydrochloric acid .
pka 2.32(at 25??)
form Crystalline Powder
color White to creamy
Odor at 100.00 %. odorless
Odor Type odorless
Water Solubility Slightly soluble in water, dilute hydrochloric acid and formic acid. Insoluble in ethanol.
Merck 14,5464
BRN 2215169
Stability: Stable. Incompatible with strong oxidizing agents. Light and air sensitive.
InChIKey WTDRDQBEARUVNC-LURJTMIESA-N
LogP -1.154 (est)
CAS DataBase Reference 59-92-7(CAS DataBase Reference)
NIST Chemistry Reference Levodopa(59-92-7)
EPA Substance Registry System Levodopa (59-92-7)
Safety Information
Hazard Codes Xn
Risk Statements 22-36/37/38-20/21/22
Safety Statements 26-36-24/25
WGK Germany 3
RTECS AY5600000
F 10-23
TSCA Yes
HS Code 29225090
Hazardous Substances Data 59-92-7(Hazardous Substances Data)
Toxicity LD50 in mice (mg/kg): 3650 ??327 orally, 1140 ??66 i.p., 450 ??42 i.v., >400 s.c.; in male, female rats (mg/kg): >3000, >3000 orally; 624, 663 i.p.; >1500, >1500 s.c. (Clark)

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