Hexa-2,4-diensure

Sorbic acid Struktur
110-44-1
CAS-Nr.
110-44-1
Bezeichnung:
Hexa-2,4-diensure
Englisch Name:
Sorbic acid
Synonyma:
sorbic;2,4-HEXADIENOIC ACID;Panosorb;Sorbistat;(E,E)-Sorbic acid;2,4-HEXANEDIENOIC ACID;hexa-2,;FEMA 3921;C6:2n-2,4;NSC 35405
CBNumber:
CB1748891
Summenformel:
C6H8O2
Molgewicht:
112.13
MOL-Datei:
110-44-1.mol

Hexa-2,4-diensure Eigenschaften

Schmelzpunkt:
132-135 °C (lit.)
Siedepunkt:
228°C
Dichte
1.2 g/cm3 at 20 °C
Dampfdruck
0.01 mm Hg ( 20 °C)
FEMA 
3921 | 2,4-HEXADIENOIC ACID, (E,E)-
Brechungsindex
1.4600 (estimate)
Flammpunkt:
127 °C
storage temp. 
2-8°C
Löslichkeit
ethanol: 0.1 g/mL, clear
Aggregatzustand
Crystalline Powder
pka
4.76(at 25℃)
Farbe
White or cream-white
PH
3.3 (1.6g/l, H2O, 20°C)
Geruch (Odor)
bland
Wasserlöslichkeit
1.6 g/L (20 ºC)
Merck 
14,8721
JECFA Number
1176
BRN 
1741831
Stabilität:
Material saturated with this acid may ignite spontaneously. Incompatible with strong oxidizing agents. May be light sensitive.
InChIKey
WSWCOQWTEOXDQX-MQQKCMAXSA-N
LogP
1.32 at 20℃
CAS Datenbank
110-44-1(CAS DataBase Reference)
NIST chemische Informationen
2,4-Hexadienoic acid, (E,E)-(110-44-1)
EPA chemische Informationen
Sorbic acid (110-44-1)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xi
R-Sätze: 36/37/38-36/38
S-Sätze: 26-36-24/25
WGK Germany  1
RTECS-Nr. WG2100000
8
Selbstentzündungstemperatur >130 °C
TSCA  Yes
HS Code  29161930
Giftige Stoffe Daten 110-44-1(Hazardous Substances Data)
Toxizität LD50 orally in rats: 7.36 g/kg (Smyth, Carpenter)
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Warnung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P302+P352, P321,P332+P313, P362
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P305+P351+P338,P337+P313P
Sicherheit
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P302+P352 BEI BERÜHRUNG MIT DER HAUT: Mit viel Wasser/... (Hersteller kann, falls zweckmäßig, ein Reinigungsmittel angeben oder, wenn Wasser eindeutig ungeeignet ist, ein alternatives Mittel empfehlen) waschen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach Möglichkeit entfernen. Weiter spülen.
P332+P313 Bei Hautreizung: Ärztlichen Rat einholen/ärztliche Hilfe hinzuziehen.
P337+P313 Bei anhaltender Augenreizung: Ärztlichen Rat einholen/ärztliche Hilfe hinzuziehen.

Hexa-2,4-diensure Chemische Eigenschaften,Einsatz,Produktion Methoden

ERSCHEINUNGSBILD

WEISSES KRISTALLINES PULVER.

PHYSIKALISCHE GEFAHREN

Staubexplosion der pulverisierten oder granulierten Substanz in Gemischen mit Luft möglich.

CHEMISCHE GEFAHREN

Schwache Säure in wässriger Lösung.

ARBEITSPLATZGRENZWERTE

TLV nicht festgelegt (ACGIH 2005).
MAK nicht festgelegt (DFG 2005).

AUFNAHMEWEGE

Aufnahme in den Körper durch Inhalation des Aerosols.

INHALATIONSGEFAHREN

Nur ungenügende Angaben vorhanden über die Geschwindigkeit, mit der eine gesundheitsschädliche Konzentration in der Luft beim Verdampfen bei 20°C erreicht wird.

WIRKUNGEN BEI KURZZEITEXPOSITION

WIRKUNGEN BEI KURZZEITEXPOSITION:
Die Substanz reizt die Augen, die Hautund die Atemwege.

WIRKUNGEN NACH WIEDERHOLTER ODER LANGZEITEXPOSITION

Wiederholter oder andauernder Hautkontakt kann zu Hautsensibilisierung führen.

LECKAGE

Verschüttetes Material in Behältern sammeln; falls erforderlich durch Anfeuchten Staubentwicklung verhindern. Reste mit viel Wasser wegspülen. Persönliche Schutzausrüstung: Atemschutzgerät, P2-Filter für schädliche Partikel.

R-Sätze Betriebsanweisung:

R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
R36/38:Reizt die Augen und die Haut.

S-Sätze Betriebsanweisung:

S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
S24/25:Berührung mit den Augen und der Haut vermeiden.

Chemische Eigenschaften

White, crystalline solid. Slightly soluble in water and many organic solvents. Combustible.

History

Sorbic acid is a white crystalline solid first isolated in 1859 by hydrolysis of the oil distilled from unripened mountain-ash berries. The name is derived from the scientific term for the rowan tree, Sorbus aucuparia Linne, which is the parent plant of the mountain ash. Sorbic acid was first synthesized in 1900. Interest in this compound was minimal until independent researchers, E. Mueller of Germany and C.M. Gooding of the United States, discovered its antimicrobial effect in 1939 and 1940, respectively. Early interest in manufacturing sorbic acid centered around its use as a tung oil replacement when tung oil supplies were curtailed in the United States during World War II. High manufacturing costs prohibited expanded use until its approval as a food preservative in 1953. Sorbic acid is widely used in foods having a pH of 6.5 or below, where control of bacteria, molds, and yeasts is essential for obtaining safe and economical storage life.

Verwenden

Sorbic Acid is an naturally occurring organic compound first isolated from unripe berries. Sorbic acid has been used as a food preservative and as an inhibitor of Clostridium Botulinum bacteria in mea t products in order to reduce the amount of nitrites which produce carcinogenic nitroamines.

Definition

ChEBI: A sorbic acid having trans-double bonds at positions 2 and 4; a food preservative that can induce cutaneous vasodilation and stinging upon topical application to humans. It is the most thermodynamically stable of the four possible geometri isomers possible, as well as the one with the highest antimicrobial activity.

Reaktionen

The chemical reactivity of sorbic acid is determined by the conjugated double bonds and the carboxyl group.
Sorbic acid is brominated faster than other olefinic acids. Reaction with hydrogen chloride gives predominately 5-chloro-3-hexenoic acid. Reactions with amines at high temperatures under pressure lead to mixtures of dehydro-2-piperidinones. A yellow crystalline complex is formed from sorbic acid and iron tricarbonyl. Similar coordination occurs also in the presence of other di- and trivalent metals. Reduction of the double bonds can produce various hexenoic acid mixtures.

Allgemeine Beschreibung

White powder or crystals. Melting point 134.5°C. Slightly acidic and astringent taste with a faint odor.

Air & Water Reaktionen

Soluble in hot water [Handbook of Chemistry and Physics]. May be sensitive to exposure to air and heat. The dust may become explosive, particularly when mixed with free-radical initiators or oxidizing agents. .

Reaktivität anzeigen

Sorbic acid may discolor on exposure to light. Can react with oxidizing agents. Also incompatible with bases and reducing agents. The dust may become explosive, particularly when mixed with free-radical initiators or oxidizing agents .

Brandgefahr

Sorbic acid is combustible.

Sicherheitsprofil

Moderately toxic by intraperitoneal and subcutaneous routes. Mildly toxic by ingestion. Experimental reproductive effects. A severe human and experimental skin irritant. Questionable carcinogen with experimental tumorigenic data. Mutation data reported. Combustible when exposed to heat or flame; can react with oxidizing materials. To fight fire, use water. When heated to decomposition it emits acrid smoke and irritating fumes.

Carcinogenicity

Wistar rats (six males) given subcutaneous injections of 2mg sorbic acid, in 0.5mL of arachis oil twice weekly for 65 weeks developed local sarcomas . The first tumor was observed at 82 weeks. Similar findings were also observed in follow-up studies . However, six Wistar rats maintained on drinking water containing 10 mg of sorbic acid/100mL drinking water for 64 weeks did not develop tumors. Tumors also were not observed inWistar rats (50 of each sex) on diets that contained 40 mg/kg/day of sorbic acid for 18 months or in 25 male and female cross-bred white mice after administration of 40 mg/kg/day for 17 months.
Mice fed a diet containing 15% sorbic acid for 88 weeks exhibited a high incidence of hepatoma. Furthermore, the glutathione level in the livers of the mice that ingested 15% sorbic acid decreased to 40% of the amount found in controls after a 3-month feeding period; this low level was maintained until the end of the experiments at 12 months. There was a close correlation between the extent of depletion of the glutathione level in the liver and the concentration of sorbic acid added to the diet. In the same strain of mice fed a diet containing 15% sorbic acid for up to 6 months, the acidic fraction of an ether extract showed slight mutagenic activity in an Ames test with Salmonella typhimurium TA98 in the presence of a liver 9000-g supernatant. Consequently, the hepatomas that developed in mice fed a 15% sorbic acid diet were considered to be induced both by the chronic depletion of the hepatic glutathione and by the gradual production of various promutagens in the intestine, which were absorbed and metabolically activated by the liver.

läuterung methode

Crystallise the acid from water. Dry it air or in a desiccator over P2O5. [Beilstein 2 IV 1701.]

Hexa-2,4-diensure Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Hexa-2,4-diensure Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

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110-44-1(Hexa-2,4-diensure)Verwandte Suche:


  • 2,4-Hexadienoic acid, (2E,4E)-
  • (e,e)-4-hexadienoicacid
  • 2,4-Hexadienoicacid,(E,E)-
  • 2e,4e-hexadienoicacid
  • 4-Hexadienoicacid,(E,E)-2
  • 2-PROPENYL ACRYLIC ACID
  • 1,3-Pentadiene-1-carboxylic acid
  • ACIDUM SORBICUM
  • (2-Butenylidene)acetic acid
  • Acetic acid, (2-butenylidene)-
  • Acetic acid, crotylidene-
  • aceticacid,(2-butenylidene)
  • aceticacid,crotylidene
  • acidesorbique
  • alpha-trans-gamma-trans-Sorbic acid
  • alpha-trans-gamma-trans-sorbicacid
  • Crotylidene acetic acid
  • crotylidene-aceticaci
  • hexa-2,
  • hexa-2,4-dienoic
  • Hexadienic acid
  • hexadienicacid
  • Hexadienoic acid
  • Hexadienoic acid, (E,E)
  • Hexadienoic acid1,3-pentadiene-1-carboxylic acid
  • hexadienoicacid
  • Kyselina 1,3-pentadien-1-karboxylova
  • Kyselina sorbova
  • kyselina1,3-pentadien-1-karboxylova
  • kyselinasorbova
  • 2,4-hexadienic acid
  • SORBICACID,POWDER,FCC
  • SORBICACID,POWDER,NF
  • SORBICACIDANDITSCOMMONSALTS
  • (E,E) 2,4-HEXADIENOIC ACID
  • FEMA 3921
  • Hexa-2,4-dienoic acid
  • RARECHEM AL BE 0146
  • SORBIC ACID
  • TRANS, TRANS-2,4-HEXADIENOIC ACID
  • Sorbinsure
  • 2,4-Hexadienoic acid, Acidum sorbicum
  • 2,4-Hexadienobic acid
  • Sorbic acid, synthesis grade
  • Sorbic acid 2g [110-44-1]
  • Sorbic acid,2,4-Hexadienoic acid,
  • Food preservative-sorbic acid in water
  • Sorbic Acid [for BiocheMical Research]
  • Sorbic Acid (1 g)
  • 2,4-Hexadienoic acid, 99% 100GR
  • Sorbic Acid (AS)
  • (E,E)-1,3-Pentadiene-1-carboxylic acid
  • C6:2n-2,4
  • NSC 35405
  • NSC 49103
  • NSC 50268
  • Sorbic acid solution
  • SORBIC ACID(RG)
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