Cannabidiol, commonly known as CBD, is a chemical compound found in the cannabis plant. It is one of more than 100 different cannabinoids present in the cannabis plant and is a major component of medical marijuana. Unlike the other major cannabinoid, tetrahydrocannabinol (THC), CBD does not produce a psychoactive effect. This makes it an attractive option for those seeking the medicinal benefits of cannabis without the associated high. In recent years, researchers have been exploring the potential therapeutic benefits of CBD and its potential applications in medical and wellness treatments. This article will explore the chemical name, properties, and potential applications of Cannabidiol.

What is the molecular formula for CBD?

The chemical name for CBD is cannabidiol, and its molecular formula is C21H30O2.

What is the scientific name for cannabidiol (CBD)?

The scientific name for cannabidiol (CBD) is 2-[(1R,6R)-3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-yl]-5-pentyl-1,3-benzenediol.

Are there any known side effects from using CBD?

The chemical name for CBD is cannabidiol. There have been some reported side effects from using CBD, such as nausea, fatigue, and irritability. However, these side effects are not common and are usually mild. It is important to speak to a healthcare professional before taking any CBD products.

What is the chemical structure of CBD?

The chemical name for CBD is cannabidiol, which is an active compound found in the cannabis plant. CBD has a molecular formula of C21H30O2 and a molecular weight of 314.46. Its chemical structure consists of a 21-carbon chain with two functional groups (the cyclohexene ring and the phenol group) attached to it.

Which CBD is pure?

CBD stands for cannabidiol, which is a chemical compound found in the Cannabis sativa plant. CBD is a non-psychoactive compound, meaning it does not produce the “high” associated with marijuana use. Pure CBD is extracted from the plant with no additional compounds or ingredients.

How is pure CBD made?

The chemical name for pure CBD is cannabidiol, which is derived from the Cannabis sativa plant. It is made through several processes, including extraction, decarboxylation, and purification. Extraction is done by using a solvent such as ethanol or CO2, to separate the CBD from other plant matter. Decarboxylation is a process where the CBD is heated and activated, to convert it into its active form. Finally, purification involves further refining the CBD to remove any impurities.

What plant is CBD from?

CBD, or cannabidiol, is a chemical compound that is found in the cannabis plant. It is one of the many active compounds that are found in the plant, and is responsible for many of its therapeutic properties.

Who invented CBD?

Cannabidiol (CBD) is a phytocannabinoid discovered in 1940 by Roger Adams, an organic chemist at the University of Illinois. It is one of some 113 identified cannabinoids in cannabis plants and accounts for up to 40% of the plant’s extract.

What is the chemical formula for CBD?

The chemical name of CBD is cannabidiol and its chemical formula is C21H30O2.

Is CBD also called hemp?

No, CBD is not the same as hemp. CBD stands for cannabidiol, which is an active compound found in the cannabis plant. Hemp is a type of cannabis plant that has high levels of CBD and low levels of THC, the main psychoactive compound in cannabis.

What is the scientific name for CBD?

The scientific name for CBD is cannabidiol. It is a naturally occurring compound found in the Cannabis sativa plant.

Network with colleagues and access the latest research in your field. ACS-Hach Programs Learn about financial support for future and current high school chemistry teachers. Find a chemistry community of interest and connect on a local and global level. Technical Divisions Collaborate with scientists in your field of chemistry and stay current in your area of specialization. Explore the interesting world of science with articles, videos and more. ChemLuminary Awards Recognizing ACS local sections, divisions and other volunteers for their work in promoting chemistry. But some THC isomers are not psychoactive and may have some beneficial uses. Members of the cannabidiol family fall into this category. There are at least seven known cannabidiol isomers. In , the iconic organic chemist Roger Adams and colleagues isolated cannabidiol as its bis 3,5-dinitrobenzoate ester from C. Israeli scientists led by Raphael Mechoulam discovered in that cannabidiol and most other cannabinoids are not psychoactive. Since then, cannabidiol has been investigated for medical uses, including treatment for a virulent form of epilepsy. It is a component of some dietary supplements and cosmetics. Biologists are working on developing marijuana strains that suppress THC content and enhance the production of cannabidiol. The regulations are so irregular that in the European Industrial Hemp Association issued a position paper that suggested a regulatory protocol with the objective that all European Union countries would operate under the same rules. The cyclopentazole anion was the Molecule of the Week for December 12, Its sodium salt was the first stable N 5 compound ever synthesized. But this salt is stable only in aqueous solution. Cannabidiol CBD is the term for a family of cannabinoids that are isomers of THC , the chief psychoactive component of marijuana. These compounds are not psychoactive, but they are useful for controlling pain and other medical conditions. Learn more about this molecule from CAS , the most authoritative and comprehensive source for chemical information. If your favorite molecule is not in our archive , please send an email to motw acs. The molecule can be notable for its current or historical importance or for any quirky reason. Thank you! Find Out More. Careers Launch and grow your career with career services and resources. Communities Find a chemistry community of interest and connect on a local and global level. Discover Chemistry Explore the interesting world of science with articles, videos and more. What molecule am I? Molecule of the Week needs your suggestions!
Cannabidiol CBD is a phytocannabinoid discovered in Cannabidiol can be taken internally in multiple ways, including by inhaling cannabis smoke or vapor , by mouth , and as an aerosol spray into the cheek. In the United States, the cannabidiol drug Epidiolex was approved by the Food and Drug Administration in for the treatment of two epilepsy disorders. Cannabidiol is the generic name of the drug and its INN. As of update , there was limited high-quality evidence for cannabidiol having a neurological effect in humans. In the United States, the FDA has indicated only one brand of prescription cannabidiol called Epidiolex for the treatment of seizures associated with Dravet syndrome , Lennox-Gastaut syndrome , or tuberous sclerosis complex in people one year of age and older. In the European Union, cannabidiol Epidyolex is indicated for use as adjunctive therapy of seizures associated with Lennox Gastaut syndrome LGS or Dravet syndrome DS , in conjunction with clobazam , for people two years of age and older. Research on other uses for cannabidiol includes several neurological disorders, but the findings have not been confirmed to establish such uses in clinical practice. Many claims are made for the therapeutic benefit of cannabidiol that are not backed by sound evidence. Some claims, such as treatment of cancer , are pseudoscience. In , the label for Epidiolex in the US was expanded to include treatment of seizures associated with tuberous sclerosis complex. Various strains of medical cannabis are found to have a significant variation in the ratios of CBD-to-THC and are known to contain other non-psychotropic cannabinoids. Certain state regulations are in place, but vary state to state. Research indicates that cannabidiol may reduce adverse effects of THC, particularly those causing intoxication and sedation , but only at high doses. Laboratory evidence indicated that cannabidiol may reduce THC clearance , increasing plasma concentrations which may raise THC availability to receptors and enhance its effect in a dose-dependent manner. Binding at this site blocks the transmembrane-spanning sodium ion translocation pathway, providing a molecular mechanism for channel inhibition, which could contribute to a reduced excitability.