Showing posts with label salts. Show all posts
Showing posts with label salts. Show all posts

Monday, September 19, 2011

New tests for 'legal marijuana,' 'bath salts' and other emerging designer drugs

 

Scientists today reported development of much needed new tests to help cope with a wave of deaths, emergency room visits and other problems from a new genre of designer drugs sold legally in stores and online that mimic the effects of cocaine, ecstasy and marijuana. They spoke at the 242nd National Meeting & Exposition of the American Chemical Society (ACS).


The reports, among more than 7,500 on the ACS agenda, focus on drugs sold as "," "plant food," "incense" and other products with colorful names, such as "Ivory Wave," "Red Dove" and "legal marijuana." They provide users with a high, but many have not yet been made illegal and are undetectable with current drug tests. In one presentation on these "legal highs," a United Kingdom researcher reported a new method to trace the source of the substances in "bath salts." In the other, a U.S. researcher discussed the challenges facing law enforcement and policy makers in regulating synthetic versions of marijuana.


Oliver Sutcliffe, Ph.D., and his collaborators reported the successful use of a method called isotope ratio mass spectrometry (IRMS) to determine who is making bath salts — drugs that can cause euphoria, paranoia, anxiety and hallucinations when snorted, smoked or injected — and which chemical companies supplied the raw materials. He and his co-workers are based at the University of Strathclyde and the James Hutton Institute in the U.K.


"With the new method, we could work backwards and trace the substances back to the starting materials," said Sutcliffe. IRMS measures the relative amounts of an element's different forms, or isotopic ratio. "This method was successful because the isotopic ratio of the starting material is transferred like a fingerprint through the synthesis," he explained.


"Bath salts" first garnered major media attention in the U.K. in early 2010, and then became a problem in the U.S. These products are not in the supermarket soap aisle — they are sold on the Internet, on the street and in stores that sell drug paraphernalia. They are sold in small individual bags for as low as $20 each for the real purpose of providing a cheap, legal high.


The powders often contain mephedrone, which is a synthetic compound, structurally related to methcathinone, which is found in Khat — a plant that is illegal in many countries, including the U.K. and the U.S. Usually, that would mean that these compounds (and derivatives thereof) would be illegal in those countries too, but because the bath salts are labeled "not for human consumption," they get around this restriction and other legislation governing the supply of medicines for human use. However, Florida and Louisiana — two hotspots of bath salts abuse — specifically banned the substances. U.K. officials banned the import of bath salts, which may lead some in the drug trade to set up clandestine labs on U.K. soil, said Sutcliffe. The new method provides law enforcement with a tool to track down these bath salts manufacturers.


In previous work, Sutcliffe developed the first pure reference standard for mephedrone, as well as the first reliable liquid chromatography test for the substance, which could be easily run in a typical law enforcement lab. The team is also developing a color-change test kit for mephedrone, which he estimates may be available by the end of the year.


In another presentation, Robert Lantz, Ph.D., from the Rocky Mountain Instrumental Laboratories, described another high that is legal in most of the U.S. — synthetic cannabinoids marketed as incense, a spice product or "legal marijuana" that give a high similar to without showing up in conventional drug tests.


"We can detect synthetic cannabinoids with modern analytical chemistry techniques, such as liquid or gas chromatography coupled to mass spectrometry, but these assays are too expensive for the 5,000-10,000 urine samples that most drug testing labs receive each day," said Lantz. Most labs screen for drugs with less expensive antibody assays, but because the structures of these substances are so dissimilar, different antibodies would likely be required for many of them, driving up the cost of a more comprehensive test.


Synthetic cannabinoid abuse rose sharply in 2010, according to U.S. poison control centers, up to 2,863 compared to only 14 in 2009. About 200 synthetic cannabinoids exist, but the U.S. Drug Enforcement Agency (DEA) banned only five of those. A handful of states, such as Washington, Georgia and Colorado, banned five of them, but they are not always the same five that the DEA banned. "The states banned several specific compounds without a particular basis for their choices," Lantz pointed out.


Colorado recently passed a law banning any substance that binds to a cannabinoid receptor in the human body. "The bill was well-intentioned, but technically, the new law not only covers synthetic cannabinoids, but also endocannabinoids, which are naturally occurring substances that the human body produces to regulate many normal processes," said Lantz.


Provided by American Chemical Society (news : web)

Saturday, September 17, 2011

New salts for chemical soups

Organozinc reagents are an important class of organometallic compounds with a wide range of applications. German chemists have developed a novel route for the synthesis of so-called organozinc pivalates in a stable powdered form. They promise to be extremely useful in many industrial contexts.

In order to meet future demands for new pharmaceuticals, innovative materials and , the chemical industry is dependent on the ongoing development of effective methods for the synthesis of complex . Because they are so versatile, organometallic molecules are of special significance in this context. Among these, reagents containing zinc atoms have certain advantages over the corresponding organolithium or -magnesium compounds, as they are compatible with a broader array of .

Ludwig-Maximilians-Universitat Munchen chemists led by Professor Paul Knochel have now developed a simple "one-pot" method for the economical synthesis of organozinc pivalates. Up until now, such functionalized organozinc compounds were only available in liquid form, and were difficult to transport and store due to their susceptibility to degradation upon contact with air or moisture. The new synthetic route permits their formation as salt-stabilized solids, which can easily be recovered in powder form. "In this form, the reagents can be stored in an argon atmosphere for months without loss of activity," says Knochel. "They can even be exposed to air for short periods without risk of degradation or ignition."

One of the most prominent applications for organozinc reagents is their use for the so-called Negishi cross-coupling, a type of reaction that provides a simple means of linking together in a virtually unlimited variety of ways, and earned its discoverer a share of the Nobel Prize for Chemistry in 2010. "The new class of organozinc pivalates makes it possible to employ different solvents in the Negishi cross-coupling reaction and greatly extends the spectrum of coupling partners it can be applied to," says Sebastian Bernhardt, who is the lead author on the new study. "The new contain magnesium salts, which also facilitate the addition of organozinc pivalates to carbonyl groups." This opens the way to their use for a whole series of applications relevant to the industrial manufacture of fine chemicals. The new scheme for synthesis of these is the subject of an international patent application. (suwe)

More information: Preparation of Solid Salt-Stabilized Functionalized Organozinc Compounds and their Application to Cross-Coupling and Carbonyl Addition Reactions
Sebastian Bernhardt, Georg Manolikakes, Thomas Kunz, Paul Knochel; Angewandte Chemie International Edition, August, 24, 2011,

Provided by Ludwig-Maximilians-Universitat Munchen

Tuesday, September 13, 2011

New tests for dangerous 'legal marijuana,' 'bath salts' and other emerging designer drugs

 Scientists report the development of much needed new tests to help cope with a wave of deaths, emergency room visits and other problems from a new genre of dangerous designer drugs sold legally in stores and online that mimic the effects of cocaine, ecstasy and marijuana.


They spoke at the 242nd National Meeting & Exposition of the American Chemical Society (ACS), being held in Denver.


The reports, among more than 7,500 on the ACS agenda, focus on drugs sold as "bath salts," "plant food," "incense" and other products with colorful names, such as "Ivory Wave," "Red Dove" and "legal marijuana." They provide users with a high, but many have not yet been made illegal and are undetectable with current drug tests. In one presentation on these "legal highs," a United Kingdom researcher reported a new method to trace the source of the substances in "bath salts." In the other, a U.S. researcher discussed the challenges facing law enforcement and policy makers in regulating synthetic versions of marijuana.


Oliver Sutcliffe, Ph.D., and his collaborators reported the successful use of a method called isotope ratio mass spectrometry (IRMS) to determine who is making bath salts -- drugs that can cause euphoria, paranoia, anxiety and hallucinations when snorted, smoked or injected -- and which chemical companies supplied the raw materials. He and his co-workers are based at the University of Strathclyde and the James Hutton Institute in the U.K.


"With the new method, we could work backwards and trace the substances back to the starting materials," said Sutcliffe. IRMS measures the relative amounts of an element's different forms, or isotopic ratio. "This method was successful because the isotopic ratio of the starting material is transferred like a fingerprint through the synthesis," he explained.


"Bath salts" first garnered major media attention in the U.K. in early 2010, and then became a problem in the U.S. These products are not in the supermarket soap aisle -- they are sold on the Internet, on the street and in stores that sell drug paraphernalia. They are sold in small individual bags for as low as $20 each for the real purpose of providing a cheap, legal high.


The powders often contain mephedrone, which is a synthetic compound, structurally related to methcathinone, which is found in Khat -- a plant that is illegal in many countries, including the U.K. and the U.S. Usually, that would mean that these compounds (and derivatives thereof) would be illegal in those countries too, but because the bath salts are labeled "not for human consumption," they get around this restriction and other legislation governing the supply of medicines for human use. However, Florida and Louisiana -- two hotspots of bath salts abuse -- specifically banned the substances. U.K. officials banned the import of bath salts, which may lead some in the drug trade to set up clandestine labs on U.K. soil, said Sutcliffe. The new method provides law enforcement with a tool to track down these bath salts manufacturers.


In previous work, Sutcliffe developed the first pure reference standard for mephedrone, as well as the first reliable liquid chromatography test for the substance, which could be easily run in a typical law enforcement lab. The team is also developing a color-change test kit for mephedrone, which he estimates may be available by the end of the year.


In another presentation, Robert Lantz, Ph.D., from the Rocky Mountain Instrumental Laboratories, described another high that is legal in most of the U.S. -- synthetic cannabinoids marketed as incense, a spice product or "legal marijuana" that give a high similar to marijuana without showing up in conventional drug tests.


"We can detect synthetic cannabinoids with modern analytical chemistry techniques, such as liquid or gas chromatography coupled to mass spectrometry, but these assays are too expensive for the 5,000-10,000 urine samples that most drug testing labs receive each day," said Lantz. Most labs screen for drugs with less expensive antibody assays, but because the structures of these substances are so dissimilar, different antibodies would likely be required for many of them, driving up the cost of a more comprehensive test.


Synthetic cannabinoid abuse rose sharply in 2010, according to U.S. poison control centers, up to 2,863 compared to only 14 in 2009. About 200 synthetic cannabinoids exist, but the U.S. Drug Enforcement Agency (DEA) banned only five of those. A handful of states, such as Washington, Georgia and Colorado, banned five of them, but they are not always the same five that the DEA banned. "The states banned several specific compounds without a particular basis for their choices," Lantz pointed out.


Colorado recently passed a law banning any substance that binds to a cannabinoid receptor in the human body. "The bill was well-intentioned, but technically, the new law not only covers synthetic cannabinoids, but also endocannabinoids, which are naturally occurring substances that the human body produces to regulate many normal processes," said Lantz.


Story Source:


The above story is reprinted (with editorial adaptations) from materials provided by American Chemical Society, via EurekAlert!, a service of AAAS.

Monday, September 12, 2011

New salts for chemical 'soups'

 Organozinc reagents are an important class of organometallic compounds with a wide range of applications. LMU chemists have developed a novel route for the synthesis of so-called organozinc pivalates in a stable powdered form. They promise to be extremely useful in many industrial contexts.


In order to meet future demands for new pharmaceuticals, innovative materials and agricultural pesticides, the chemical industry is dependent on the ongoing development of effective methods for the synthesis of complex organic compounds. Because they are so versatile, organometallic molecules are of special significance in this context. Among these, reagents containing zinc atoms have certain advantages over the corresponding organolithium or -magnesium compounds, as they are compatible with a broader array of functional groups.


LMU chemists led by Professor Paul Knochel have now developed a simple "one-pot" method for the economical synthesis of organozinc pivalates. Up until now, such functionalized organozinc compounds were only available in liquid form, and were difficult to transport and store due to their susceptibility to degradation upon contact with air or moisture.


The new synthetic route permits their formation as salt-stabilized solids, which can easily be recovered in powder form. "In this form, the reagents can be stored in an argon atmosphere for months without loss of activity," says Knochel. "They can even be exposed to air for short periods without risk of degradation or ignition."


One of the most prominent applications for organozinc reagents is their use for the so-called Negishi cross-coupling, a type of reaction that provides a simple means of linking carbon atoms together in a virtually unlimited variety of ways, and earned its discoverer a share of the Nobel Prize for Chemistry in 2010. "The new class of organozinc pivalates makes it possible to employ different solvents in the Negishi cross-coupling reaction and greatly extends the spectrum of coupling partners it can be applied to," says Sebastian Bernhardt, who is the lead author on the new study. "The new reagents contain magnesium salts, which also facilitate the addition of organozinc pivalates to carbonyl groups."


This opens the way to their use for a whole series of applications relevant to the industrial manufacture of fine chemicals. The new scheme for synthesis of these compounds is the subject of an international patent application.


The research is reported in Angewandte Chemie International Edition, early view (Aug. 24, 2011).


Story Source:


The above story is reprinted (with editorial adaptations ) from materials provided by Ludwig-Maximilians-Universität München.

Journal Reference:

Sebastian Bernhardt, Georg Manolikakes, Thomas Kunz and Paul Knochel. Preparation of Solid Salt-Stabilized Functionalized Organozinc Compounds and their Application to Cross-Coupling and Carbonyl Addition Reactions. Angewandte Chemie International Edition, 2011 DOI: 10.1002/anie.201104291