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Dipropyl methane

Synonyms Dipropyl methane heptyl hydride heptane... [Pg.368]

SYNS DIPROPYL METHANE EPTANI (ITALL N) GETTYSOLVE-C HEPTAN (POLISH) n-HEPTANE O HEPTANEN (DUTCH) HEPTYL HYDRIDE... [Pg.708]

DIPROPYLENETRIAMINE see AIX250 DIPROPYL ETHER see PNMOOO DIPROPYL KETONE see DWT600 DIPROPYL MERCURY see DWUOOO DIPROPYL METHANE see HBC500 DI-n-PROPYLNITROSAXflNE see NKB700 DIPROPYLNITROSOAMINE see NKB700 DIPROPYL OXIDE see PNMOOO DIPROPYLOXOSTANNANE see DWVOOO... [Pg.1655]

Synonyms n-Heptane Dipropyl methane Getty-solve-C Heptyl hydride Heptan (Polish) Eptani (Italian) Heptanen (Dutch) UN1206 (DOT) Chemical/Pharmaceutical/Other Class Aliphatic hydrocarbon... [Pg.1315]

DIPROPYL METHANE (142-82-5) CtH, Highly flammable liquid. Forms explosive mixture with air [explosion limits in air (vol %) 1 to 7.0 flash point 25°F/-4°C autoignition temp 433°F/223°C Fire Rating 3]. Violent reaction with strong oxidizers ... [Pg.416]

Synonyms Alkane C7 Dipropyl methane n-Heptane Heptyl hydride Clas cation Sat. aliphatic hydrocarbon Empirical CjHk Fmnula CH,(CH2)5CH,... [Pg.1136]

Dipropyl hexanedioate. See Dipropyl adipate Dipropyl ketone. See 4-Heptanone Dipropyl methane. See Heptane Di-n-propyl peroxydicarbonate CAS 16066-38-9... [Pg.1513]

Dipropylene glycol tallowamine. See PPG-2 tattowamine Dipropyl methane. See Heptane DIPS. See Diisopropyl sebacate... [Pg.2098]

Synonyms Altene C7 Dipropyl methane n-Heptane Heptyl hydride Classification Sat. aliphatic hjrtrocarbon Empirical C H g Formula CH3(CH2)5CH3... [Pg.2146]

Alkyl sulfides and thiols. Some alkyl thiols and sulfides, notably those from commonly ingested Allium sativum (garlic) and Allium cepa (onion) (Alliaceae), are variously bioactive as odorants and antimicrobials. Propanethial S-oxide (CH3-CH2-CH=S=0) is a lachrymatory irritant principle of onion. Allicin (S-oxodiallydisulfide CH2=CH—CH2-SO-S-CH2— CH=CH2), diallyldisulfide (CH2=CH-CH2-S-S-CH2-CH=CH2) and diallylsulfide (CH2=CH—CH2—S—CH2-CH=CH2) are major odorants of garlic that are reactive and irritant because of the allyl groups. Dimethyl disulfide (CH3—S—S-CH3), dipropyl disulfide (CH3-CH2-CH2-S-S-CH2-CH2-CH3), methyl allyl disulfide (CH3-S-S-CH2-CH=CH2) and propane-1-thiol (CH3-CH2—CH2—SH) are further Allium odorants. Methane thiol (methyl mercaptan CH3—SH) is a widespread plant volatile and notably derives from anaerobic bacterial degradation of cysteine as in human flatus and bad mouth odour. The aliphatic disulfides allicin and ajoene inhibit proinflammatory expression of iNOS. [Pg.47]

Dithiophosphonsaure Methan- -di-methylamid-(ethylthio-methyl-ester) XII/1, 598 Trithiophosphorsanre -dipropyl-amid XII/2, 794... [Pg.332]

Unlike formamidine, acetamidine and benzamidine react with both aromatic and aliphatic a-hydroxyketones to give imidazoles exclusively. It has been suggested that aryl groups favour the enolic form (2) of the tautomeric mixture, resulting in the formation of oxazoles as major products. Aliphatic groups favour the keto form (1), from which imidazoles are derived. That amidines more complex than formamidine favour imidazole formation may be a consequence of steric hindrance to reaction of the enolic hydroxy groups with the amidine carbon in (2). The general reaction has been used to prepare such compounds as 4,5-dipropyl imidazole (25% yield from tris(formylamino)-methane and 5-hydroxyoctan-4-one), and a variety of 2-imidazolones and 2-aminoimidazoles [8]. The fact that oxazoles can be converted into imidazoles with some ease extends the applicability of this reaction. [Pg.135]

Grignard s fundamental investigations,92 as well as subsequent very extensive studies, have shown that the solvent plays an important part in the reaction of organic halides with magnesium. Diethyl ether has proved the most serviceable solvent in the majority of cases, but dipropyl, dibutyl, and diisopentyl ether, as well as dioxan and tetrahydrofuran have been used in special cases formals, e.g., diisopropoxy- and diisobutoxy-methane, may also be invoked in the synthesis of organomagnesium compounds.93... [Pg.763]

C Ha Wnadeaubm-fl.lS) 1 II249. 4.7.Dipropyl-deoadien-(3.7)-in-(5) 11129.. >l)inie y).d-phenyl-o tan 6, 470. TWproPyl-phenyl-methan 6 1 227. Methyl-diisobutyl-phenyl.methan 6 1227. d.f-Dlmethyl-a-[3-methyl-oyciohexen-(4)-yl]-a.e(oderx.0-belita n 6 1 227. Diamylbenzol 5, 470. 1.3.6-Triinethyl-2-n-heptyl-benzol 6, 471. Penta thylbenzol 6. 471, 1227, II368. [Pg.1108]

Verbindung CuHa Oa, vielleicht Dipropyl-dibenzo methan o I 107 vgl. a. 7 T 406., yDioxo ./ bis-[2.4.6-trimethyl.pheayJ] propan 7, 779. [Pg.1438]

GuHg Tetnulecadijn-<6.8) 1II 248. n-Octyl benzol 6, 463,1 215, II 343. fi-Methyl-ri-pbenyl-beptan i. 464. Uiptopyl-benzyl-inetban 5 1215. Dimethyl-isoamyl-phmyl-methaa 5 1215. Metbyl-dipropyl-Tdietiyl-methan 51216. Dibthyl-propyl-pnenyl-methan 5 1215. [Pg.2448]


See other pages where Dipropyl methane is mentioned: [Pg.1094]    [Pg.1979]    [Pg.3475]    [Pg.1671]    [Pg.1094]    [Pg.1979]    [Pg.3475]    [Pg.1671]    [Pg.913]    [Pg.913]    [Pg.24]    [Pg.981]   
See also in sourсe #XX -- [ Pg.368 ]




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4.5- Dipropyl

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