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CAS-Nr. | 112-80-1 |
Bezeichnung: | |
Englisch Name: | cis-9-Octadecenoic acid |
Synonyma: | 9-Octadecensäure 9,10-Octadecensäure Oleinsäure cis-9-Octadecensäure k52;G18;D100;K 52;SOCS;(cis);NAA35;FORMOL;groco2;groco4 |
CBNumber: | CB7228241 |
Summenformel: | C18H34O2 |
Molgewicht: | 282.46 |
MOL-Datei: | 112-80-1.mol |
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cis-9-Octadecenoic acid physikalisch-chemischer Eigenschaften |
Schmelzpunkt:: |
13-14 °C(lit.)
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Dichte: |
1.09 g/mL at 25 °C(lit.)
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Dampfdichte: |
1.03 (vs air)
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Dampfdruck: |
52 mm Hg ( 37 °C)
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Brechungsindex: |
n20/D 1.377
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Wasserlöslichkeit: |
negligible |
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Sensitive : |
Air Sensitive |
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Stabilität:: |
Stable. Combustible. Incompatible with strong oxidizing agents, aluminium. |
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cis-9-Octadecenoic acid Chemische Eigenschaften,Einsatz,Produktion Methoden |
Chemische Eigenschaften colourless to light yellow viscous liquid |
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Verwenden Oleic acid is a monounsaturated omega-9 fatty acid. Oleic Acid is obtained by the hydrolysis of various animal and vegetable fats and oils. Oleic Acid is used as an emulsifying or solubilizing agent i
n aerosol products. |
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Allgemeine Beschreibung Colorless to pale yellow liquid with a mild odor. Floats on water. |
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ERSCHEINUNGSBILD FARBLOSE FLüSSIGKEIT, VERFäRBT SICH GELB BIS BRAUN BEI KONTAKT MIT LUFT. |
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Air & Water Reaktionen Keep cis-9-Octadecenoic acid well closed; protect cis-9-Octadecenoic acid from air and light. . May form peroxides upon exposure to air. This is taken to account for an explosion that occurred, by the mixing of the acid with aluminum, [J. Chem. Educ., 1956, 36, 308]. Water Insoluble. |
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CHEMISCHE GEFAHREN Schwache Säure. |
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ARBEITSPLATZGRENZWERTE TLV nicht festgelegt. MAK: Krebserzeugend Kategorie 3A; (DFG 2008).
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Reaktivität anzeigen cis-9-Octadecenoic acid is a carboxylic acid. Carboxylic acids donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in cis-9-Octadecenoic acid to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions. |
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Health Hazard Industrial use of compound involves no known hazards. Ingestion causes mild irritation of mouth and stomach. Contact with eyes or skin causes mild irritation. |
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INHALATIONSGEFAHREN Verdampfen bei 20°C vernachlässigbar; eine belästigende Partikelkonzentration in der Luft kann jedoch beim Versprühen schnell erreicht werden. |
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WIRKUNGEN BEI KURZZEITEXPOSITION WIRKUNGEN BEI KURZZEITEXPOSITION: Die Substanz reizt leicht die Augen und die Haut. |
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Brandgefahr cis-9-Octadecenoic acid is combustible. |
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LECKAGE Ausgelaufene Flüssigkeit in abgedeckten Behältern sammeln. Verschüttete Flüssigkeit mit viel Wasser wegspülen.
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R-Sätze Betriebsanweisung: R23/24/25:Giftig beim Einatmen, Verschlucken und Berührung mit der Haut. R34:Verursacht Verätzungen. R40:Verdacht auf krebserzeugende Wirkung. R43:Sensibilisierung durch Hautkontakt möglich. R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut. R38:Reizt die Haut. |
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S-Sätze Betriebsanweisung: S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen. S37/39:Bei der Arbeit geeignete Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen. S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren. S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen. |
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cis-9-Octadecenoic acid Anbieter Lieferant Produzent Hersteller Vertrieb Händler. Global( 253)Lieferanten |
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ALDEHYDE C1
112-80-1
Carcinogens
Carboxylic Acid Salts
Chiral Building Blocks
Carbohydrates
Cancer Research
Carbonyl Compounds
C1 to C6
BioChemika Ultra
Biological Buffers
Asymmetric Synthesis
Building Blocks
Biochemicals and Reagents
Analytical Reagents
Analytical Standards
Analytical Chromatography Product Catalog
Aldehydes
Alphabetic
BioChemical
METHYL ALDEHYDE
METHANONE
FORMALDEHYDE DEVELOPING SOLUTION
FORMALIN, CARSONS
FORMALIN, NEUTRAL
FORMALIN NEUTRAL BUFFER
FORMALDEHYDE SOLUTION
FORMALDEHYDI
FORMALDEHYDE, BUFFERED
FORMALDEHYDE, CARSON-MILLON
FORMALDE-FRESH
FORMALDE-FRESH SOLUTION
FORMALDE-FRESH SOLUTION, BUFFERED
FORMIC ALDEHYDE
FORMOL
FORMALIN, NEUTRAL BUFFERED
FORMALIN NEUTRAL SODIUM SALT
PHARMALINK COUPLING REAGENT
NBF FIXATIVE
MORBICID
MILDFORM(R) 20N
MILDFORM(R) 20NM
MILDFORM(R) 10N
MILDFORM(R) 10NM
MILDFORM(R) 15N
MILDFORM(R) 15NM
Synthetic Reagents
Solvents
Solvents, Buffers and Reagents for Luminescence
Reagents
Plant Molecular Biology
Plant Biotechnology
Puriss p.a. ACS
Puriss p.a.
Nucleic Acid Purification
Organic Building Blocks
Monosaccharide
Molecular Biology
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