Oil Based Steroids Safe Organic uaiacol Natural Edible Perfume Light Yellow Liquild Powerful Hormone Solvent

Oil Based Steroids Safe Organic uaiacol Natural Edible Perfume Light Yellow Liquild Powerful Hormone Solvent

Product Name: Guaiacol

Synonyms: PYROCATECHOL MONOMETHYL ETHER;PYROGUAIAC ACID;O-METHOXYPHENOL;O-METHYLCATECHOL;O-HYDROXYANISOLE;CATECHOL MONOMETHYL ETHER;Gulaiacol;GUAJACOL
CAS: 90-05-1
MF: C7H8O2
MW: 124.14
EINECS: 201-964-7
Product Categories: Pharmaceutical Intermediates;Aromatic Ethers;Aromatics Compounds;Antioxidant;Biochemistry;Aromatics;ANASTIL
MP 26-29 °C(lit.)
Bp 205 °C(lit.)
Density 1.129 g/mL at 25 °C(lit.)
Vapor density 4.27 (vs air)
Vapor pressure 0.11 mm Hg ( 25 °C)
Refractive index n20/D 1.543(lit.)
FEMA 2532
Fp 180 °F
Storage temp. Refrigerator
Chemical Properties Light Yellow Oil
Content : 99%
HS code : 29095010
Key Words : Guaiacol , guaiacol sulfonate , guaiacol oxidation indicator , guaiacolate , guaiacol hydrogen peroxide , guaiacol glyceryl ether , guaiacol reaction .

Employ:

Allowed edible perfume. Natural Guaiacol is used in confect a series of essence of coffee, herb, fumes and tobacco. Natural Guaiacol is also use as perfume and antioxidants in food and daily chemicals synthesize vanillin and pharmaceutical intermediates. General Description Colorless to amber crystals or liquid. Density (of solid) 1.129 g / cm3. Solidifies at 28°C (82.4°F), but may remain liquid for a long time even at a much lower temperature. Slightly water soluble. Soluble in aqueous sodium hydroxide. Used medicinally as an expectorant. Used, because of its anti-oxidant properties, as an anti-skinning agent for paints. Air & Water Reactions Sensitive to air and light (darkens). Slightly water soluble.
Reactivity Profile: Guaiacol may react with oxidizing materials. Guaiacol forms salts readily with bases.
Fire Hazard Guaiacol is combustible.

Uses and chemical reactions:

Guaiacol is a precursor to various flavorants, such as eugenol and vanillin.An estimated 85% of the worlds supply of vanillin comes from guaiacol. The route entails condensation of glyoxylic acid with guaiacol to give mandelic acid, which is oxidized to produce a phenylglyoxylic acid. This acid undergoes a decarboxylation to afford vanillin.

Safety:

Methoxyphenols are potential biomarkers of biomass smoke exposure, e.g., from inhalation of woodsmoke. Dietary sources of methoxyphenols overwhelm the contribution from inhalational exposures to woodsmoke.

Locust pheromone:

Guaiacol is produced in the gut of desert locusts, Schistocerca gregaria, by the breakdown of plant material. This process is undertaken by the gut bacterium Pantoea agglomeransa (Enterobacter). It is one of the main components of the pheromones that cause locust swarming.