The synthesis occurs in acid conditions which protonate the amino group, the NaHCO3 lowers the pH so that the amino group is no longer protonated.
I believe a chloride salt of the benzocaine is the product as the HCl acid attacks the amine functional group. however ethanol may also be formed from the hydrolysis of the ester and create a carboxyl group attached to the benzene ring. This will leave two products at the end of the reaction. I myself need some clarification on the resulting products whether it be a mixture of 2 products or one product.
The amino group on p-aminobenzoic acid is typically protected during the synthesis of benzocaine to prevent unwanted reactions and ensure the desired product is formed. Removing the amino group would lead to the formation of unwanted byproducts. Protecting the amino group allows for selective reactions to take place at other functional groups on the molecule.
Drying benzocaine helps to remove any moisture present, which can affect its purity and stability. Moisture can also promote bacterial growth, leading to contamination and degradation of the compound. Overall, drying benzocaine ensures its quality and effectiveness in various applications.
No, Benzocaine does not contain alcohol. It is a local anesthetic commonly used in over-the-counter products like topical creams or sprays to relieve pain and itching. Benzocaine works by blocking nerve signals in the body to numb the area where it is applied.
Ethanol is used in the preparation of benzocaine as a solvent to dissolve and extract the benzocaine from its raw material. It helps to achieve a uniform distribution of the active ingredient and aids in the formulation process.Ethanol also acts as a preservative to extend the shelf life of the final product.
Solid NaHCO3 is used instead of aqueous NaHCO3 in the synthesis of tert-butyl chloride because solid NaHCO3 helps to absorb any excess acid produced during the reaction, preventing side reactions and ensuring the desired product is obtained. Using solid NaHCO3 also allows for better control of the reaction conditions and facilitates the separation of the organic layer containing tert-butyl chloride.
No, benzocaine is an ester.
Benzocaine is a local anesthetic used to numb skin and mucous membrane. Benzocaine hydrochloride is the hydrochloride salt form of benzocaine, which is more water-soluble than benzocaine and may have different pharmacokinetic properties. Benzocaine hydrochloride is often used in pharmaceutical formulations that require water solubility.
A benzocaine is a local anaesthetic used as a topical pain reliever.
Yes, so make sure you use it whenever you have pain.
if the police want to use it as conspiracy to supply? depends on how much benzo
sodium bicarbonate
Oh, dude, smoking benzocaine? That's a hard pass. It's a local anesthetic, not some cool party drug. Plus, inhaling any kind of smoke that's not meant for smoking is just asking for trouble. Stick to the classics, like, I don't know, breathing regular air or something.
I believe a chloride salt of the benzocaine is the product as the HCl acid attacks the amine functional group. however ethanol may also be formed from the hydrolysis of the ester and create a carboxyl group attached to the benzene ring. This will leave two products at the end of the reaction. I myself need some clarification on the resulting products whether it be a mixture of 2 products or one product.
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You don't. Generally, drug dealers use the benzocaine for making fake crack, not the real thing. Benzocaine numbs the mouth when tasted, just like cocaine. Do keep in mind that manufacturing street drugs is illegal, and manufacturing counterfeit drugs is not only illegal, but can put the dealer at risk for retaliation.
to shift the reaction toward the products (Benzocaine) to counteract the imposed change excess reactants so that will lead to a higher percentage of Benzocaine. according to Le Chatelier's principle