Showing posts with label Advanced chemical. Show all posts
Showing posts with label Advanced chemical. Show all posts

Tuesday, June 5, 2012

An Introduction of Phenylacetone

 Phenylacetone

Item name: Phenylacetone
CAS:1 03-79-7
Molecular Weight: 134.18g/mol
Molecular Formula: C9H10O

Phenylacetone (known also as phenyl-2-propanone, benzyl methyl ketone, or methyl benzyl ketone), is an organic compound. It is a clear oil with a refractive index of 1.5168. This substance is used in the manufacture of methamphetamine and amphetamine as a starting material or intermediate, where it is commonly known as P2P. Due to the illicit uses in clandestine chemistry, it was declared a schedule II controlled substance in the United States 11 February 1980.

Phenylacetone can also be produced from many other compounds. For example:
•phenylacetic acid is distilled with lead acetate or calcium acetate to yield phenylacetone.
•benzaldehyde is reacted with nitroethane yielding phenyl-2-nitropropene, which is reduced, usually in the presence of acid, to phenylacetone.
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Monday, June 4, 2012

History of Artemisinin

Artemisia annua has been used by Chinese herbalists for more than two thousand years in the treatment of many illnesses, such as skin diseases and malaria. The earliest record dates back to 200 BC, in the "Fifty-two Prescriptions" unearthed from the Mawangdui Han Dynasty tombs. Its antimalarial application was first described, in Zhouhou Beiji Fang ("The Handbook of Prescriptions for Emergencies"), edited in the middle of the fourth century by Ge Hong. In that book, 43 malaria treatment methods were recorded.

 artemisinin In the 1960s, a research program, under the name Project 523, was set up by the Chinese army to find an adequate treatment for malaria. In 1972, in the course of this research, Tu Youyou discovered artemisinin in the leaves of Artemisia annua (annual wormwood). The drug is named Qinghaosu (Chinese: 青蒿素) in Chinese. It was one of many candidates then tested by Chinese scientists from a list of nearly 5000 traditional Chinese medicines for treating malaria. It was not only the only one that was effective, but it was found to clear malaria parasites from patients' bodies faster than any other drug in history. Artemisia annua is a common herb and has been found in many parts of the world, including along the Potomac River, in Washington, D.C. Images of the original scientific papers are available online and a book, Zhang Jianfang, "Late Report – Record of Project 523 and the Research and Development of Qinghaosu", Yangcheng Evening News Publisher 2007 was published in 2006, which records the history of the discovery.
It remained largely unknown to the rest of the world for about seven years, until results were published in the Chinese Medical Journal in 1979. The report was met with skepticism at first, partly because the chemical structure of artemisinin, particularly the peroxide, appeared to be too unstable to be a viable drug.
For many years after the discovery, access to the purified drug and the plant from which it was extracted were restricted by the Chinese government. It was not until the late 1970s and early 80s that news of the discovery reached scientists outside China. The World Health Organisation (WHO) tried to contact Chinese scientists and officials to find out more, but drew a blank. Ying Lee, one of the scientists involved in the research into artemisinin, said the Chinese distrusted the West. The Chinese suspected the West just wanted to exploit the drug and sell it around the world slightly altered and repatented. The fact that there were several Americans on the WHO's steering board on malaria and that some were from the military did not help clear the distrust. It can be noted Americans had just invested a lot into mefloquine, an analogue of quinine.

In 2006, after artemisinin had become the treatment of choice for malaria, the WHO called for an immediate halt to single-drug artemisinin preparations in favor of combinations of artemisinin with another malaria drug, to reduce the risk of parasites developing resistance.

In 2011, Tu was awarded the prestigious Lasker-DeBakey Clinical Medical Research Award for her discovery. The discovery of artemisinin is reportedly being considered for a Nobel Prize in Medicine.

Project 523 developed, in addition to artemisinin, a number of products that are used in combination with artemisinin, including lumefantrine, piperaquine, and pyronaridine.

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Sunday, June 3, 2012

What Is Piperonal?

 Piperonal

Piperonal, also known as heliotropin, is an organic compound that is commonly found in fragrances and flavors. The molecule is structurally related to benzaldehyde and vanillin. It exists as a white or colorless solid. It has a floral odor commonly described as being similar to that of vanillin and cherry. It is used as flavoring and in perfumes.

Item name: Piperonal
CAS: 120-57-0
Molecular Weight: 150.13g/mol
Molecular Formula: C8H6O3

Piperonal is an aromatic aldehyde that comes as transparent crystals, C8H6O3, and has a floral odor. It is used as flavoring and in perfume. It can be obtained by oxidation of piperonyl alcohol or the reduction of piperic acid. It is also a minor natural component of the extract of vanilla. It is a common in inexpensive synthetic vanilla flavor and candies.

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Wednesday, May 30, 2012

Simple Description of 4-(1,3-Benzodioxol-5-yl)-2-Butanone

 4-(1,3-benzodioxol-5-yl)-2-butanone


Butanone, also known as methyl ethyl ketone or MEK, is an organic compound with the formula CH3C(O)CH2CH3. This colorless liquid ketone has a sharp, sweet odor reminiscent of butterscotch and acetone. It is produced industrially on a large scale, and also occurs in trace amounts in nature. It is soluble in water and is commonly used as an industrial solvent.

Butanone is biosynthesized by some trees and found in some fruits and vegetables in small amounts. It is released to the air from car and truck exhausts.

Item name: 4-(1,3-benzodioxol-5-yl)-2-butanone
CAS: 55418-52-5
Molecular Weight: 192.21g/mol
Molecular Formula: C11H12O3
Description: 4-(1,3-benzodioxol-5-yl)-2-butanone is a pale yellow liquid.It is soluble in organic solvents such as ethanol, but insoluble in water. It is always used for the floral fragrance of flavor enhancer.

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Tuesday, May 29, 2012

The Explanation of Lysergol

 Lysergol
Lysergol, is an alkaloid of the ergoline family that occurs as a minor constituent in some species of fungi (most within Claviceps), and in the morning glory family of plants (Convolvulaceae), including the hallucinogenic seeds of Rivea corymbosa (ololiuhqui), Argyreia nervosa (Hawaiian baby woodrose) and Ipomoea violacea. Lysergol is not a controlled substance in the USA. Its possession and sale is also legal under the U.S. Federal Analog Act because of it does not have a known pharmacological action or a precursor relationship to LSD, which is a controlled substance. However, lysergol can be utilized as an intermediate in the manufacture of some ergoloid medicines (e.g., nicergoline).

Item name: Lysergol
CAS :602-85-7
Molecular Weight :254.33g/mol
Molecular Formula: C16H18N2O

Lysergol is a colorless needle crystal or white crystalline powder. It is odorless and tasteless.It is perishable in case of light or air.

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Friday, May 25, 2012

Pharmacokinetics of Nimetazepam

 Nimetazepam

Nimetazepam (marketed under brand name Erimin) is an intermediate-acting hypnotic drug which is a benzodiazepine derivative. It was first synthesized by a team at Hoffmann-La Roche in 1962. It possesses hypnotic, anxiolytic, sedative, and skeletal muscle relaxant properties.

Taken orally, nimetazepam has very good bioavailability with nearly 100% being absorbed from the gut. It is among the most rapidly absorbed and quickest acting oral benzodiazepines, and hypnotic effects are typically felt within 15–30 minutes after oral ingestion. The blood level decline of the parent drug was biphasic with the short half-life ranging from 0.5-0.7 hours and the terminal half-life from 8–26.5 hours (mean 17.25 hours). It is the N-methylated analogue of nitrazepam (Mogadon, Alodorm), to which it is partially metabolised. Nitrazepam has a long elimination half-life, so effects of repeated dosage tend to be cumulative.

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