Lidocaine Hydrochloride CAS# 73-78-9
Lidocaine hydrochloride is an anesthetic as well as an antiarrhythmic drug. Clinically, it is mainly used for infiltration anesthetic, epidural anesthetic, topical anesthesia (consisting of mucosal anesthetic throughout thoracoscopic examination or abdominal surgical treatment) as well as nerve conduction block. It can additionally be used for early ventricular tightenings and also ventricular tachycardia after acute myocardial infarction, and also for ventricular arrhythmias triggered by digitalis poisoning, cardiac surgery as well as cardiac catheterization. But it is usually inadequate for supraventricular arrhythmias.
Lidocaine Hydrochloride CAS# 73-78-9
| Lidocaine hydrochloride Basic information |
| General?Physical and chemical properties?Local anesthetic and antiarrhythmic drugs?Application?Metabolism?Indications?Usage and dosage?Adverse effect?Additional information?Medicine interactions?Precautions?References |
| Product Name: | Lidocaine hydrochloride |
| Synonyms: | Lidocaine hydrochloride CP2000,BP98;a-(diethylamino)-26-acetoxylidideHCl;a-(diethylamino)-26-acetoxylididehydrochloride;2-(Diethylamino)-N-(2,6-dimethylphenyl)-acetamide hydrochloride;6??-acetoxylidide,2-(diethylamino)-2hydrochloride;6??-acetoxylidide,2-(diethylamino)-2monohydrochloride;Acetamide,2-(diethylamino)-N-(2,6-diethylphenyl)-,monohydrochloride;Acetamide,2-(diethylamino)-N-(2,6-dimethylphenyl)-,monohydrochloride |
| CAS: | 73-78-9 |
| MF: | C14H23ClN2O |
| MW: | 270.8 |
| EINECS: | 200-803-8 |
| Product Categories: | Pharma materials;Pharmaceutical intermediates;Amines;Aromatics;Research Chemical;Intermediates & Fine Chemicals;Pharmaceuticals;API;Others;73-78-9 |
| Mol File: | 73-78-9.mol |
 |
|
| Lidocaine hydrochloride Chemical Properties |
| Melting point | 80-82??C |
| storage temp. | Inert atmosphere,2-8??C |
| form | Solid |
| color | White to off-white |
| Water Solubility | Water : ?? 36 mg/mL (132.94 mM) |
| InChI | InChI=1S/C14H22N2O.ClH/c1-5-16(6-2)10-13(17)15-14-11(3)8-7-9-12(14)4;/h7-9H,5-6,10H2,1-4H3,(H,15,17);1H |
| InChIKey | IYBQHJMYDGVZRY-UHFFFAOYSA-N |
| SMILES | C(NC1=C(C)C=CC=C1C)(=O)CN(CC)CC.[H]Cl |
| LogP | 2.359 (est) |
| CAS DataBase Reference | 73-78-9(CAS DataBase Reference) |
| EPA Substance Registry System | Acetamide, 2-(diethylamino)-N-(2,6-dimethylphenyl)-, monohydrochloride (73-78-9) |
Related Products
Chemical Name: Semaglutide
CAS No.: 910463-68-2
Molecular Formula: C187H291N45O59
Molecular Weight: 4113.57754
Appearance: Powder
Chemical Name: Imazalil Sulfate
CAS No.: 58594-72-2
Molecular Formula: C14H14Cl2N2O.H2SO4
Molecular Weight: 395.26
Appearance: Solid
Chemical Name: Ammonium Iron(II) Sulfate
Synonyms: Diammonium iron bis(sulphate); iron (ii) ammonium sulfate
CAS No.: 10045-89-3
Molecular Formula: FeH5NO4S
Molecular Weight: 170.95
Chemical Name: Marbofloxacin
CAS No.: 115550-35-1
Molecular Formula: C17H19FN4O4
Molecular Weight: 362.36
Appearance: Red-Brown Crystal
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.
Chemical Name: Arabic gum
CAS No.: 9000-01-5
Appearance: powder
Product name:Cyclopentane
Purity:96%
Appearance:White powder
Package:25kg/bag
Sample:Available
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.
Urapidil is a sympathetic antihypertensive drug. It acts as ?? 1 ?C adrenoceptor antagonists and 5-HT 1A receptor agonists act. Although the initial report showed that urapidil was also a ?? 2 ?C adrenoceptor agonist, which was not confirmed in later studies, proved that it had no agonist effect in the saphenous vein of dogs and ileum of guinea pigs. With others ?? Unlike 1-adrenoceptor villains, urapidil does not cause response tachycardia, which may be connected to its weak ?? 1-adrenoceptor antagonist activity and its impact on heart vagal drive. Urapidil has actually not been approved by the US Food and drug administration, yet it is offered in Europe.
Urapidil (URA), chemical name is 6-[[3-[4-(2-methoxyphenyl)-1-piperazinyl]propyl]amino]-1,3-dimethyl -2,4(1H,3H)-pyrimidinedione, trade name: ebrantil (ebrantil), synonym: excellent matchi, uracil substituted by phenazine.
Chemical Name: STODDARD SOLVENT
CAS No.: 64742-88-7
Appearance: Colorless or Light Yellow Liquid
Chemical Name: Quercetin-3-O-sophoroside
CAS No.: 18609-17-1
Molecular Formula: C27H30O17
Molecular Weight: 626.52
Chemical Name: Abemaciclib
CAS No.: 1231929-97-7
Molecular Formula: C27H32F2N8
Molecular Weight: 506.59
