TOLUALDEHYDES

TOLUALDEHYDES Basic information
Product Name:TOLUALDEHYDES
Synonyms:METHYLBENZALDEHYDE;TOLUALDEHYDE;TOLUALDEHYDES;tolyl;TOLUALDEHYDES(MIXEDORTHO,META,PARA);ar-Tolualdehyde;tolualdehydes, mixture;TOLUALDEHYDES (MIXED O,M,P)
CAS:1334-78-7
MF:C7H6O
MW:106.12194
EINECS:215-615-1
Product Categories:
Mol File:1334-78-7.mol
TOLUALDEHYDES Structure
TOLUALDEHYDES Chemical Properties
Boiling point 164.15°C (rough estimate)
density 0.9651 (rough estimate)
FEMA 3068 | TOLUALDEHYDES (MIXED O,M,P)
refractive index 1.4800 (estimate)
Odorat 1.00 % in dipropylene glycol. sweet cherry chemical coumarin powdery
Odor Typefruity
JECFA Number866
LogP2.26
EPA Substance Registry SystemMethylbenzaldehyde (1334-78-7)
Safety Information
Hazardous Substances Data1334-78-7(Hazardous Substances Data)
ToxicityLD50 oral in rat: 2250mg/kg
MSDS Information
TOLUALDEHYDES Usage And Synthesis
Chemical PropertiesColorless liquid. Slightly soluble inwater; soluble in alcohol and ether. There are also oand misomers. Combustible.
Chemical PropertiesTolualdehydes, mixed o-, m-, p-, have a sweet and herbaceous odor reminiscent of bitter almond.
OccurrenceReported found in roasted nuts, tomato, cooked beef, beef fat, cider, coffee, tea and elderberry juice.
UsesPerfumes, pharmaceutical and dyestuff intermediate, flavoring agent.
PreparationBy oxidation of o-, m-, or p-xylene (chemical or electrolytical oxidation).
Taste threshold valuesTaste characteristics at 15 ppm: cherry pit, coumarin, almond, sweet, with a slight powdery hay and vanillalike nuance.
MetabolismAromatic aldehydes are oxidized in vivo almost entirely to the corresponding acid. Thus, in rabbits, p-tolualdehyde is converted to p-toluic acid which has been detected in the urine as the ester glucuronide (Williams, 1959). p-Tolualdehyde was oxidized to p-toluic acid by resting cells of Pseudomonas aeruginosa (Omori & Yamada, 1970). Perillaldehyde dehydrogenase, isolated from a soil pseudomonad, catalysed the oxidation of m- and p-tolualdehyde but not of o-tolualdehyde (Ballal, Bhattacharyya & Rangachari, 1967). The reduction of p-tolualdehyde by NADH was catalysed by horse-liver alcohol dehydrogenase (Blomquist, 1966) and by yeast alcohol dehydrogenase at pH 8.5-9.5 (Klinman, 1975). A non-specific NADPH-linked aldehyde reductase isolated from various areas of bovine brain also catalysed the reduction of p-tolualdehyde (Tabakoff & Erwin, 1970).
TOLUALDEHYDES Preparation Products And Raw materials
Raw materialsXylene
Preparation Productsleather seasoning agent DLC-1-->Acitretin
Aluminum acetylacetonate METHYL ISOCYANOACETATE TRIS(2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONATO)EUROPIUM(III) N-BUTYLISOCYANIDE PHENYLSELENOL Tris(2,4-pentanedionato)chroMiuM(III) DICHLORO(ETHYLENEDIAMINE)PLATINUM(II) SALCOMINE 2,4-PENTANEDIONE, SILVER DERIVATIVE Tosylmethyl isocyanide COBALT(II) ACETYLACETONATE Cupric acetylacetonate Ethyl isocyanoacetate TERT-BUTYL ISOCYANIDE Ferric acetylacetonate COBALT ETHYLENE DIAMINE CHLORIDE Benzyl isocyanide TRIS(2,2,6,6-TETRAMETHYL-3,5-HEPTANEDIONATO)DYSPROSIUM(III)

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