Capric-Alkohol 99% siehe COA Kanbei

1-Decanol

1-Decanol;Decylalkohol; Capric Alkohol; Caprinalkohol;n-Decylalkohol; Nonylcarbinol; Sipol L 10; Alfol 10; T 148;n-Decanol;Decanol; Antak; Epal 10;1-Hydroxydecan; Royaltac; Kalcohl 10H; Conol 10N; Nakol 10-99; Kalcohl 1098; Nakol 10; Nafol 10; NSC 406313; Kalcol 1098; Nafol 10D; Kalcohl 10; Conol 1098; Lorol C 10-98; Capryl Alkohol; Lorol C 10

112-30-1

C10H22O

InChIKey=MWKFXSUHUHTGQN-UHFFFAOYSA-N

158.28

158.28

1735221

203-956-9

89V4LX791F

1490

406313

1987|3082

DTXSID7021946|DTXSID3034589|DTXSID2028301

Colorless to water-white liquid|Colorless, viscous, refractive liquid|Moderately viscous, strongly refractive liquid

29051900

Heterocyclischer Ring

20.2

4.6

Clear colorless to slightly yellow Liquid

0.8297 g/cm³ @ Temp: 20 °C

6,4 °C

232.9 °C @ Presse: 760 Torr

180 °F

1.436-1.438

H2O: insoluble ;ethanol: soluble 60%, clear, colorless (1mL/3mL)

room temp

1 mm Hg ( 70 °C)

4.5 (vs air)

Oral-Rat LD50: 4720 mg/kg; Oral-Mouse LD50: 6500 mg/kg

Brennbar; Verbrennung erzeugt reizende Dämpfe

0,9-5,7% (V)

Sweet odor

LEICHTER, CHARAKTERISTISCHER FETTIGER GESCHMACK

3.20e-05 atm-m3/mole|Henry's Law constant = 4.7831X10-5 atm-cu m/mol at 25 °C

Solidifies /at 6.4 °C/, forming rectangular plates or leaflets|Conversion factors: 1 mg/L= 154.5 ppm; 1 ppm= 6.47 mg/cu m at 25 °C, 760 mm Hg|Liquid molar volume = 0.191772 cu m/kmol|Heat of formation = -4.0166X10%2B8 J/kmol|For more Other Experimental Properties (Complete) data for 1-DECANOL (7 total), please visit the HSDB record page.

Unlöslich in Wasser.

Alkohole und Polyole

DECYL ALCOHOL attacks plastics. REF [Handling Chemicals Safely, 1980. p. 236]. Acetyl bromide reacts violently with alcohols or water, [Merck 11th ed., 1989]. Mixtures of alcohols with concentrated sulfuric acid and strong hydrogen peroxide can cause explosions. Example: An explosion will occur if dimethylbenzylcarbinol is added to 90% hydrogen peroxide then acidified with concentrated sulfuric acid. Mixtures of ethyl alcohol with concentrated hydrogen peroxide form powerful explosives. Mixtures of hydrogen peroxide and 1-phenyl-2-methyl propyl alcohol tend to explode if acidified with 70% sulfuric acid, [Chem. Eng. News 45(43):73(1967); J, Org. Chem. 28:1893(1963)]. Alkyl hypochlorites are violently explosive. They are readily obtained by reacting hypochlorous acid and alcohols either in aqueous solution or mixed aqueous-carbon tetrachloride solutions. Chlorine plus alcohols would similarly yield alkyl hypochlorites. They decompose in the cold and explode on exposure to sunlight or heat. Tertiary hypochlorites are less unstable than secondary or primary hypochlorites, [NFPA 491 M, 1991]. Base-catalysed reactions of isocyanates with alcohols should be carried out in inert solvents. Such reactions in the absence of solvents often occur with explosive violence, [Wischmeyer(1969)].

550 °F (USCG, 1999)|550 °F (288 °C)|255 °C

-9980 cal/g

Entflammbarkeitsgrenzen = 0,7 bis 5,5 Vol.-%

NICHT KORROSIV

81,50 kJ/mol bei 225 °C

Kritische Temperatur: 690 K; kritischer Druck: 2,3 MPa| Kritische Temperatur = 690,00 ° K; Kritischer Druck = 2,3700X10%2B6 Pa