What is methoxyphenol used for?

What is methoxyphenol used for?

4-Methoxyphenol is an active ingredient and used in dermatology. It is employed as a pharmaceutical drug in skin depigmentation. It is used as polymerization inhibitors. For example, in the radical polymerization of acryaltes and styrene monomers.

What is the structure of methoxy phenol?

3-Methoxyphenol

PubChem CID 9007
Structure Find Similar Structures
Molecular Formula C7H8O2
Synonyms 3-METHOXYPHENOL 150-19-6 m-Methoxyphenol 3-Hydroxyanisole m-Hydroxyanisole More…
Molecular Weight 124.14

Is 4-methoxyphenol flammable?

ICSC 1097 – 4-METHOXYPHENOL. Combustible. Finely dispersed particles form explosive mixtures in air. NO open flames.

What kind of compound is guaiacol?

organic compound
Guaiacol (/ˈɡwaɪəkɒl/) is a naturally-occurring organic compound with the formula C6H4(OH)(OCH3). Although it is biosynthesized by a variety of organisms, this aromatic oil is usually derived from guaiacum or wood creosote….Guaiacol.

Names
CAS Number 90-05-1
3D model (JSmol) Interactive image
ChEBI CHEBI:28591
ChEMBL ChEMBL13766

What is catechol used for?

Uses. Approximately 50% of the synthetic catechol is consumed in the production of pesticides, the remainder being used as a precursor to fine chemicals such as perfumes and pharmaceuticals. It is a common building block in organic synthesis.

What is the density of 2 Methoxyphenol?

1.11 g/cm³
Guaiacol/Density

What is the function of resorcinol?

Resorcinol is a 1,3-isomer (or meta-isomer) of benzenediol with the formula C6H4(OH)2. It is used as an antiseptic and disinfectant in topical pharmaceutical products in the treatment of skin disorders and infections such as acne, seborrheic dermatitis, eczema, psoriasis, corns, calluses, and warts.

Is methoxy a functional group?

A methoxy group is the functional group consisting of a methyl group bound to oxygen. This alkoxy group has the formula O–CH3. On a benzene ring, the Hammett equation classifies a methoxy substituent at the para position as an electron-donating group, but as an electron-withdrawing group if at the meta position.

What is Mehq inhibitor?

Inhibitors such as MEHQ (monomethyl ether hydroquinone) and PTZ (phenothiazine) are added to acrylic acid in the shipping and storage process to prevent its spontaneous polymerization. Dissolved oxygen is also an strong inhibitor, and its presence in the solution enhances the inhibition effects of MEHQ.

Is methoxyphenol more acidic than phenol?

It increases electron density on the benzene ring and does not delocalize negative charge of phenoxide ion. It decreases acidity. So, now we should know that p−methoxyphenol is less acidic than phenol.

What is guaiacol found in?

Guaiacol is a phenolic natural product first isolated from Guaiac resin and the oxidation of lignin. Guaiacol is also present in wood smoke, as a product of pyrolysis of lignin. Guaiacol has been found in the urine of patients with neuroblastoma and pheochromocytoma.

Is guaiacol a substrate?

With guaiacol as substrate, acidic pH optima have often been reported for the apoplastic peroxidases of several plant species (Hendriks et al., 1991; Melo et al., 1996; Nair and Showalter, 1996).

What kind of light does 4-methoxyphenol absorb?

Phenol absorbs at wavelengths >290 nm (4) and therefore, by analogy, 4-methoxyphenol may be susceptible to direct photolysis by sunlight (SRC). 4-Methoxyphenol has been observed to photodegrade in pure water exposed to sunlight (5).

What does 4 methoxyphenol smell like in water?

IDENTIFICATION: 4-Methoxyphenol is a colorless to white waxy solid. It smells like caramel and phenol. 4-Methoxyphenol is very soluble in water. It has been found in licorice root and sesame seed. Other names for this chemical include 4-hydroxyanisole, p-hydroxyanisole, and hydroquinone methyl ether.

What is the role of P-methoxyphenol in phenols?

P-methoxyphenol is a member of phenols and a member of methoxybenzenes. It has a role as a metabolite. 4-methoxyphenol Computed by LexiChem 2.6.6 (PubChem release 2019.06.18)

What is the half life of 4-methoxyphenol?

The rate constant for the vapor-phase reaction of 4-methoxyphenol with photochemically-produced hydroxyl radicals has been measured as 9.5X10-11 cu cm/molecule-sec at 21 deg C(1). This corresponds to an atmospheric half-life of about 4 hours at an atmospheric concentration of 5X10+5 hydroxyl radicals per cu cm(2).

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