Hive Newbee Forum

	Main Index Search Register Login Who's Online FAQ Links
	Main Index Search Register Login Who's Online FAQ Links

	2 Online, 0 Active		You are not logged in

This is a historical archiveThe forum is read-only. Private information has been removed. It is not possible to login.

	Newbee Forum	Thread: Previous Forum index

All 3 posts Subject: C6H5-OH + H2S2O8 Please login to post Down

acx01b
(Hive Bee)
11-04-04 00:15
No 539532
User Picture       C6H5-OH + H2S2O8

hi, i founded that:

PHENOL

Molecular formula: C6H6O
   CAS registry number: 108-95-2
RTEC registry number: SJ 3325000 (solid)

------------------------------------------------------------------------------------------------------------------------------
PHYSICAL PROPERTIES    OTHER CHARACTERISTICS
------------------------------------------------------------------------------------------------------------------------------

Relative molecular mass 94.11 White crystalline solid turning pink or red when
Melting point (°C)    40.9    exposed to air and light; burning taste and
Boiling point (°C)    181.75    distinctive odour; the compound reacts moderately
Water solubility (g/litre)    67    fast with oxidizing agents and violently with
Specific density (25°C) 1.071 butadiene, peroxydisulfuric acid, peroxymono-
Relative vapour density 3.24    sulfuric acid, and aluminium chloride + nitro-
Vapour pressure (kPa) (20°C)    0.04 (0.357 mmHg) benzene; when heated or burning the compound
Ignition temperature (°C) 715 emits toxic fumes; the compound is extremely
Flash point (closed cup) (°C) 80    destructive to mucous membranes, skin, and eyes
Flammability (explosive) and may be fatal if inhaled, swallowed, or absorbed
limits (vol. %) 1.3-9.5 through the skin

what is the reaction between Ph-OH and H2S2O8 ?
i guess Ph-X reacts same way ?

jboogie
(Hive Bee)
11-04-04 02:22
No 539563
      other fun facts to know about phenol

Disposition in the Body.Rapidly absorbed from the gastrointestinal tract and readily penetrates the skin. It is metabolised by conjugation to yield phenyl glucuronide and phenyl sulfate; small amounts are oxidised to catechol and quinol which are also conjugated. Oxidation of these metabolites to quinones may tint the urine green.(hehehe) laugh Acid–labile phenol conjugates are present endogenously in serum at concentrations of about 0.1 mg/L. Phenol is a metabolite of benzene. Endogenous phenol concentrations in urine average about 5 to 10 mg/L.
Toxicity.Phenol denatures and precipitates cellular proteins and thus may cause rapid poisoning. The minimum lethal dose by mouth is about 1 g. Severe and even fatal poisoning may also arise from absorption of phenol from open wounds or through the intact skin. The maximum permissible atmospheric concentration is 5 ppm.

Don't you think if I had something intelligent to say, it would bee in my post?

yei
(Hive Bee)
11-10-04 18:11
No 540870
      It gets oxidized to quinones

preferably p-benzoquinone.

This reaction doesn't work for Ph-X, and anyway, if you have that you can use if for better things.

_{It's good to bee back! Don't trust your computer!!}

	https://the-hive.archive.erowid.org	the-hive@erowid.org



Powered by Holy Rollers Release 3.00, © 2020-2023, Rhodium's Global Fanclub International. All rights reserved.
Links Erowid Rhodium

	All 3 posts		Subject: C6H5-OH + H2S2O8		Please login to post		Down


		acx01b (Hive Bee) 11-04-04 00:15 No 539532				C6H5-OH + H2S2O8
						hi, i founded that: PHENOL Molecular formula: C6H6O CAS registry number: 108-95-2 RTEC registry number: SJ 3325000 (solid) ------------------------------------------------------------------------------------------------------------------------------ PHYSICAL PROPERTIES OTHER CHARACTERISTICS ------------------------------------------------------------------------------------------------------------------------------ Relative molecular mass 94.11 White crystalline solid turning pink or red when Melting point (°C) 40.9 exposed to air and light; burning taste and Boiling point (°C) 181.75 distinctive odour; the compound reacts moderately Water solubility (g/litre) 67 fast with oxidizing agents and violently with Specific density (25°C) 1.071 butadiene, peroxydisulfuric acid, peroxymono- Relative vapour density 3.24 sulfuric acid, and aluminium chloride + nitro- Vapour pressure (kPa) (20°C) 0.04 (0.357 mmHg) benzene; when heated or burning the compound Ignition temperature (°C) 715 emits toxic fumes; the compound is extremely Flash point (closed cup) (°C) 80 destructive to mucous membranes, skin, and eyes Flammability (explosive) and may be fatal if inhaled, swallowed, or absorbed limits (vol. %) 1.3-9.5 through the skin what is the reaction between Ph-OH and H2S2O8 ? i guess Ph-X reacts same way ?



		jboogie (Hive Bee) 11-04-04 02:22 No 539563				other fun facts to know about phenol
						Disposition in the Body.Rapidly absorbed from the gastrointestinal tract and readily penetrates the skin. It is metabolised by conjugation to yield phenyl glucuronide and phenyl sulfate; small amounts are oxidised to catechol and quinol which are also conjugated. Oxidation of these metabolites to quinones may tint the urine green.(hehehe) Acid–labile phenol conjugates are present endogenously in serum at concentrations of about 0.1 mg/L. Phenol is a metabolite of benzene. Endogenous phenol concentrations in urine average about 5 to 10 mg/L. Toxicity.Phenol denatures and precipitates cellular proteins and thus may cause rapid poisoning. The minimum lethal dose by mouth is about 1 g. Severe and even fatal poisoning may also arise from absorption of phenol from open wounds or through the intact skin. The maximum permissible atmospheric concentration is 5 ppm. Don't you think if I had something intelligent to say, it would bee in my post?



		yei (Hive Bee) 11-10-04 18:11 No 540870				It gets oxidized to quinones
						preferably p-benzoquinone. This reaction doesn't work for Ph-X, and anyway, if you have that you can use if for better things. _{It's good to bee back! Don't trust your computer!!}

All 3 posts	End of thread	Top