Citronellal

Citronellal Struktur
106-23-0
CAS-Nr.
106-23-0
Bezeichnung:
Citronellal
Englisch Name:
Citronellal
Synonyma:
Citronella;RHODINAL;3,7-dimethyl-6-octena;3,7-dimethyloct-6-enal;3,7-DIMETHYL-6-OCTENAL;Citronellel;CITRONELLAL NATURAL;CitroneL;FEMA 2307;d-rhodinal
CBNumber:
CB3715673
Summenformel:
C10H18O
Molgewicht:
154.25
MOL-Datei:
106-23-0.mol

Citronellal Eigenschaften

Schmelzpunkt:
-16°C (estimate)
alpha 
D25 +11.50°
Siedepunkt:
207 °C(lit.)
Dichte
0.857 g/mL at 25 °C(lit.)
Dampfdruck
14 hPa (88 °C)
Brechungsindex
n20/D 1.451(lit.)
FEMA 
2307 | CITRONELLAL
Flammpunkt:
169 °F
storage temp. 
Store below +30°C.
Löslichkeit
Chloroform (Soluble), Methanol (Sparingly)
Aggregatzustand
Liquid
Farbe
Clear light yellow
Wichte
0.858 (20/4℃)
PH
7 (H2O)
Geruch (Odor)
at 10.00 % in dipropylene glycol. sweet dry floral herbal waxy aldehydic citrus
Geruchsart
floral
Explosionsgrenze
1.2-4.5%(V)
Wasserlöslichkeit
Slightly miscible with water and ethanol.
Sensitive 
Air Sensitive
Merck 
14,2329
JECFA Number
1220
BRN 
1720789
Stabilität:
Hygroscopic
InChIKey
NEHNMFOYXAPHSD-UHFFFAOYSA-N
LogP
3.62 at 25℃
CAS Datenbank
106-23-0(CAS DataBase Reference)
NIST chemische Informationen
6-Octenal, 3,7-dimethyl-(106-23-0)
EPA chemische Informationen
Citronellal (106-23-0)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher Xn,Xi,N
R-Sätze: 38-43-51/53-36/37/38-22
S-Sätze: 36/37-61-37/39-26-36
RIDADR  UN 3082 9/PG 3
WGK Germany  3
RTECS-Nr. RH2140000
8
Selbstentzündungstemperatur 202 °C
TSCA  Yes
HS Code  29121900
Giftige Stoffe Daten 106-23-0(Hazardous Substances Data)
Toxizität LD50 orally in Rabbit: 2420 mg/kg LD50 dermal Rabbit > 2500 mg/kg
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
H317 Kann allergische Hautreaktionen verursachen. Sensibilisierung der Haut Kategorie 1A Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
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
P261 Einatmen von Staub vermeiden.
P264 Nach Gebrauch gründlich waschen.
P264 Nach Gebrauch gründlich waschen.
P272 Kontaminierte Arbeitskleidung nicht außerhalb des Arbeitsplatzes tragen.
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.

Citronellal Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R38:Reizt die Haut.
R43:Sensibilisierung durch Hautkontakt möglich.
R51/53:Giftig für Wasserorganismen, kann in Gewässern längerfristig schädliche Wirkungen haben.
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.
R22:Gesundheitsschädlich beim Verschlucken.

S-Sätze Betriebsanweisung:

S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
S61:Freisetzung in die Umwelt vermeiden. Besondere Anweisungen einholen/Sicherheitsdatenblatt zu Rate ziehen.
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.

Chemische Eigenschaften

(?)-Citronellal occurs in Java citronella oil at a concentration of 35%. Racemic citronellal is the main constituent of E. citriodora oil with a content of up to 85%.
Pure citronellal is a colorless liquid with a refreshing odor, reminiscent of lemon balm. Upon catalytic hydrogenation, citronellal yields dihydrocitronellal, citronellol, or dihydrocitronellol, depending on the reaction conditions. Protection of the aldehyde group, followed by addition of water to the double bond in the presence of mineral acids or ion-exchange resins results in the formation of 3,7-dimethyl-7-hydroxy-octan-l-al (hydroxydihydrocitronellal). Acid-catalyzed cyclization to isopulegol is an important step in the synthesis of (?)-menthol.

Occurrence

The d-form of citronellal has been reported in the oil of citronella (Ceylon, Jammus, Kaschmis), in the oil from leaves of Barosma pulchella, in the oil from roots of Phebalium nudum and in the oils of Eucalyptus citriodora, Leptospermum citratum and Baeckea citriodora. The /-form is present in the oils of Backhousia citriodora var. A, E. citriodora, Litsea cubeba (fruits) and lemongrass. Citronellal is generally present also in the oils of lemon, mandarin, Lavandula delphinensis, Ocimum canum f. citrata and many others (Fenarolis Handbook of Flavor Ingredients, 1971).

Verwenden

rac-Citronellal is a monoterpenoid and the major isolate in citronella oil. Citronella oil is an essential oil bearing insecticidal properties. rac-Citronellal is also often used as a fragrance ingred ient.

synthetische

Citronellal is still isolated from essential oils in considerable quantities; it is also produced synthetically.
1) Isolation from essential oils:(+)-Citronellal is obtained from citronella oils by fractional distillation. Racemic citronellal is isolated from E. citriodora oil; when necessary, it is purified by using an addition compound, for example, the bisulfite derivative.
2) Synthesis from geraniol or nerol: Racemic citronellal can be obtained by vaporphase rearrangement of geraniol or nerol in the presence of, for example, a barium-containing copper–chromium oxide catalyst.
3) Synthesis from citronellol: Racemic citronellal can also be obtained by dehydrogenation of citronellol under reduced pressure with a copper chromite catalyst.
4) Synthesis from citral: Selective hydrogenation of citral to citronellal can be accomplished in the presence of a palladium catalyst in an alkaline alcoholic reaction medium. A continuously operating process for the hydrogenation on a palladium catalyst in the presence of trimethylamine has been developed.
5) Synthesis from myrcene: (+)- and (?)-Citronellal are available from myrcene via geranyldiethylamine, which is enantioselectively isomerized to (+)- or (?)-citronellalenamine. Hydrolysis yields pure (+)- or (?)-citronellal; see monograph menthol.

Definition

ChEBI: A monoterpenoid, the main component of citronella oil which gives it its distinctive lemon aroma.

Essential oil composition

Citronella oil contains a number of fragrant fractions of which citronellal, geraniol and citronellol are the major components. Ceylon citronella oil contains 55 to 65% total acetylizable alcohols (calculated as citronellol) and 7 to 15% total aldehyde (calculated as citronellal). The main constituents are geraniol (18 to 20%), citronellol (6.4 to 8.4%), citronellal (5 to 15%), geranyl acetate (2%); limonene (9 to 11%) and methyl isoeugenol (7.2 to 11.3%). Other constituents are camphene, caryophyllene, linalool, citral (neral and geranial), methylheapenone, methyleugenol, l-borneol, nerol, eugenol and farnesol.* Java citronella oil contains not less than 35% alcohols (calculated as citronellol) and not less than 35% aldehydes (calculated as citronellal). The Java type appears to have higher concentrations of citronellol (35%) and geraniol (21%) than does the Ceylon type (citronellol 10% and geraniol 18%).

Allgemeine Beschreibung

(±)-Citronellal was studied for its fumigant antifungal activity against Pyricularia (Magnaporthe) grisea.

Stoffwechsel

Feeding 50 g citronellal to rabbits was followed by the isolation of 13 g of a crystalline glucuronide, which proved to be p-menthane-3.8-diol-D-glucuronide. The citronellal appeared to have been cyclized and the glucuronide obtained was identical with that obtained on feeding p-menthane-3,8-diol (menthoglycol) (Kühn & Low, 1938). However, evidence was produced to show that the cyclization was not, strictly speaking, a biological reaction, but a chemical one which took place in the stomach under the influence of the gastric hydrochloric acid. The conjugation of the menthoglycol with glucuronic acid was, of course, a purely biological reaction. It was found that on shaking 20 g citronellal with 200 ml 0-5% HCl for 48 hr at 37 C, 12 g menthoglycol was formed (Kühn & Low, 1938).

Citronellal Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Citronellal Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 432)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hebei Mojin Biotechnology Co., Ltd
+8613288715578
sales@hbmojin.com China 12456 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512
info@tianfuchem.com China 21691 55
career henan chemical co
+86-0371-86658258
sales@coreychem.com China 29914 58
SHANDONG ZHI SHANG CHEMICAL CO.LTD
+86 18953170293
sales@sdzschem.com China 2931 58
Hubei Jusheng Technology Co.,Ltd.
18871490254
linda@hubeijusheng.com CHINA 28180 58
Hebei Guanlang Biotechnology Co., Ltd.
+86-19930503282
alice@crovellbio.com China 8823 58
Xiamen AmoyChem Co., Ltd
+86-592-6051114 +8618959220845
sales@amoychem.com China 6387 58
Xi'an Kono chem co., Ltd.,
029-86107037 13289246953
info@konochemical.com China 2995 58
Hubei xin bonus chemical co. LTD
86-13657291602
linda@hubeijusheng.com CHINA 22968 58
Shandong chuangyingchemical Co., Ltd.
18853181302
sale@chuangyingchem.com CHINA 5909 58

106-23-0(Citronellal)Verwandte Suche:


  • 2,3-Dihydrocitral
  • d-rhodinal
  • Levo-citronellal
  • 3,7-DIMETHYL-6-OCTEN-1-AL
  • (+/-)-3,7-DIMETHYL-6-OCTENAL
  • (+/-)-CITRONELLAL
  • CITRONELLAL
  • CITRONELLAL 80
  • FEMA 2307
  • CITRONELLAL NATURAL 85+% FCC
  • (+/-)-CITRONELLAL, 80-90%
  • Citronellal, pract., 93%
  • citronellal,3,7-dimethyl-6-octenal,rhodinal
  • CITRONELLAL FCC, NATURAL
  • CITRONELLAL SYNTHETIC
  • CITRONELLAL, (-)-(SG)
  • Citronellal,85+%,tech.
  • Citronellal,93%,pract.
  • CITRONELLAL FOR SYNTHESIS 100 ML
  • rac-Citronellal
  • (+/-)-Citronellal >=95.0% (GC)
  • Citronellal 3,7-Dimethyl-6-octenal
  • 6-ocetnal,3,7-dimethyl-
  • 6-octenal,3,7-dimethyl-
  • 6-Octenal,3,7-dimethyl-,(±)-
  • b-citronellal
  • dl-Citronellal
  • CITRONELLAL FOR SYNTHESIS 500 ML
  • Citronellal for synthesis
  • CitroneL
  • Rhodinal (Citronellal)
  • Methoprene Impurity 6
  • Citronellal USP/EP/BP
  • RHODINAL
  • 3,7-dimethyl-6-octena
  • 3,7-dimethyloct-6-enal
  • 3,7-DIMETHYL-6-OCTENAL
  • CITRONELLAL NATURAL
  • Citronella
  • Citronellel
  • 3,7-dimethyloct-6-en-1-al
  • GLY-HIS-LYS ACETATE SALT 72957-37-0
  • 106-23-0
  • 5949-05-03
  • 5949-5-3
  • C9H17CHO
  • CH32CCHCH2CH2CHCH3CH2CHO
  • Organic Building Blocks
  • Building Blocks
  • Analytical Standards
  • Alphabetic
  • Analytical Chromatography Product Catalog
  • Carbonyl Compounds
  • C10 to C21
  • CI - CL
  • Aldehydes
  • Furans ,Coumarins
Copyright 2019 © ChemicalBook. All rights reserved