What makes octyl benzoate?

Octyl benzoate, also known as octyl benzoic acid, is a member of the class of compounds known as benzoic acid esters. Benzoic acid esters are ester derivatives of benzoic acid. Octyl benzoate is practically insoluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa).

What is the common name for benzoate?

Sodium benzoate is the sodium salt of benzoic acid, widely used as a food preservative and pickling agent….Sodium benzoate.

What kind of compound is benzoate?

Benzoate is the simplest member of the class of benzoates that is the conjugate base of benzoic acid, comprising a benzoic acid core with a proton missing to give a charge of -1. It has a role as a human xenobiotic metabolite and a plant metabolite. It is a conjugate base of a benzoic acid.

Is benzoate a solid?

Benzoic acid (CAS No. 65-85-0) is a white solid that is slightly soluble in water. Sodium benzoate (CAS No. 532-32-1) is about 200 times more soluble in water.

Is benzyl benzoate toxic to humans?

Benzyl benzoate can be a skin irritant when used as a topical scabicide. Overdose can result in blistering and hives or a rash can occur as an allergic reaction.

Is benzoic acid toxic?

Benzoic acid is non-toxic and stable under ordinary conditions. While occupational exposure limits have not been established, benzoic acid may still pose a health risk and, therefore, the safe work practices should always be followed: Wash hands thoroughly after handling.

What are the side effects of benzyl benzoate?

Side Effects

• Blister formation, crusting, itching, oozing, reddening, or scaling of skin.
• difficulty in urinating (dribbling)
• jerking movements.
• sudden loss of consciousness.

How often should you apply benzyl benzoate?

Adults—Use just one time. For severe cases, treatment may be repeated two or three times after twenty-four hours. For infants: Use mixed with three parts of water, just one time. For older children: Use mixed with an equal quantity of water, just one time.

What is the side effect of sodium benzoate?

Despite potential benefits, sodium benzoate can have side effects, including nausea, vomiting, and abdominal pain ( 2 , 18 ). Additionally, medicinal doses of sodium benzoate may deplete your body of the amino acid carnitine, which plays a critical role in energy production.

Should I avoid sodium benzoate?

While sodium benzoate is considered safe, scientists have shown that negative side effects occur when it’s mixed with ascorbic acid (vitamin C). Their studies indicate that it then turns into benzene, a known carcinogen that may cause cancer.

Is benzoic acid safe for human consumption?

Benzoic Acid and Sodium Benzoate are generally recognized as safe in foods according to the U.S. Food and Drug Administration.

What kind of chemical is 2-ethylhexyl 4-benzoate?

https://www.epa.gov/tsca-inventory. EPA Chemicals under the TSCA. The drug is the 2-ethylhexyl ester of p- (dimethylamino) benzoic acid, occurs as a clear to yellow, oily liquid having a faint aromatic odor and is insoluble in water and soluble in alcohol.

What are the dangers of 2-ethyl hexyl benzoate?

PubMed: Rodent thyroid, liver, and fetal testis toxicity of the monoester metabolite of bis- (2-ethylhexyl) tetrabromophthalate (tbph), a novel brominated flame retardant present in indoor dust. PubMed: Influence of penetration enhancer on drug permeation from volatile formulations.

Which is a benzoate ester used in sunscreen?

Padimate O is a benzoate ester. Padimate O is an active sunscreen agent in cosmetics and over-the-counter sunscreen drug products in concentrations up to 8%, as regulated by the FDA. It is a structurally-related compound to [DB02362] that absorbs UV-B rays to prevent photodamage.

Which is a structurally related compound to db02362?

It is a structurally-related compound to [DB02362] that absorbs UV-B rays to prevent photodamage. It penetrates human skin, and is shown to induce non-ligatable strand breaks on DNA in vitro and mutagenic effects on yeast i n vivo. Computed by LexiChem 2.6.6 (PubChem release 2019.06.18)