Chemical Formula: C6H6O

Chemical Formula C6H6O

Found 12 metabolite its formula value is C6H6O

Phenol

Hydroxybenzene

C6H6O (94.0418626)


D - Dermatologicals > D08 - Antiseptics and disinfectants > D08A - Antiseptics and disinfectants > D08AE - Phenol and derivatives C - Cardiovascular system > C05 - Vasoprotectives > C05B - Antivaricose therapy > C05BB - Sclerosing agents for local injection An organic hydroxy compound that consists of benzene bearing a single hydroxy substituent. The parent of the class of phenols. R - Respiratory system > R02 - Throat preparations > R02A - Throat preparations > R02AA - Antiseptics D019999 - Pharmaceutical Solutions > D012597 - Sclerosing Solutions N - Nervous system > N01 - Anesthetics > N01B - Anesthetics, local D000890 - Anti-Infective Agents D002317 - Cardiovascular Agents D004202 - Disinfectants CONFIDENCE standard compound; INTERNAL_ID 225

   

Benzene oxide

7-oxabicyclo[4.1.0]hepta-2,4-diene

C6H6O (94.0418626)


   

Phenol

Phenolated water for disinfection

C6H6O (94.0418626)


Phenol, is a toxic, colourless crystalline solid with a sweet tarry odor that resembles a hospital smell. It is commonly used as an antiseptic and disinfectant. It is active against a wide range of micro-organisms including some fungi and viruses, but is only slowly effective against spores. It has been used to disinfect skin and to relieve itching. Phenol is also used in the preparation of cosmetics including sunscreens, hair dyes, and skin lightening preparations. It is also used in the production of drugs (it is the starting material in the industrial production of aspirin), weedkillers, and synthetic resins. Phenol can be found in areas with high levels of motor traffic, therefore, people living in crowded urban areas are frequently exposed to traffic-derived phenol vapor. The average (mean +/- SD) phenol concentration in urine among normal individuals living in urban areas is 7.4 +/- 2.2 mg/g of creatinine. Exposure of the skin to concentrated phenol solutions causes chemical burns which may be severe; in laboratories where it is used, it is usually recommended that polyethylene glycol solution is kept available for washing off splashes. Notwithstanding the effects of concentrated solutions, it is also used in cosmetic surgery as an exfoliant, to remove layers of dead skin (Wikipedia). In some bacteria phenol can be directly synthesized from tyrosine via the enzyme tyrosine phenol-lyase [EC:4.1.99.2]. It can be produced by Escherichia and Pseudomonas. Phenol has been identified as a uremic toxin according to the European Uremic Toxin Working Group (PMID: 22626821). It is used as a flavouring agent in a few foods, at maximum levels below 10 ppm

   

Oxepin

Oxepenes

C6H6O (94.0418626)


   

Phenol-13C6

Phenol-13C6

C6H6O (94.0418626)


   

Phenol-14C6

Phenol-14C6

C6H6O (94.0418626)


   

3-prop-2-ynoxyprop-1-yne

3-prop-2-ynoxyprop-1-yne

C6H6O (94.0418626)


   
   

(E)-hex-2-en-4-ynal

(E)-hex-2-en-4-ynal

C6H6O (94.0418626)


   

(Z)-hex-2-en-4-ynal

(Z)-hex-2-en-4-ynal

C6H6O (94.0418626)


   

Phenol-d5

Phenol-d5

C6H6O (94.0418626)


   

Benzene oxide

Benzene oxide

C6H6O (94.0418626)