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Key Documents

Altri documenti

27470

Sigma-Aldrich

(±)-Citronellal

≥95.0% (GC)

Sinonimo/i:

(±)-3,7-Dimethyl-6-octenal

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About This Item

Formula condensata:
(CH3)2C=CHCH2CH2CH(CH3)CH2CHO
Numero CAS:
106-23-0
Peso molecolare:
154.25
Beilstein:
1720789
Numero CE:
203-376-6
Numero MDL:
MFCD00038090
Codice UNSPSC:
12352100
ID PubChem:
57648246
NACRES:
NA.22

Livello qualitativo

100

Saggio

≥95.0% (GC)

Forma fisica

liquid

Indice di rifrazione

n20/D 1.451 (lit.)

P. eboll.

207 °C (lit.)

Densità

0.857 g/mL at 25 °C (lit.)

Stringa SMILE

CC(CC\C=C(\C)C)CC=O

InChI

1S/C10H18O/c1-9(2)5-4-6-10(3)7-8-11/h5,8,10H,4,6-7H2,1-3H3
NEHNMFOYXAPHSD-UHFFFAOYSA-N

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Categorie correlate

Descrizione generale

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

Applicazioni

(±)-Citronellal was used to inhibit the development of mechanical nociception induced by carrageenan (CG) and tumor necrosis factor-α (TNF-α).

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315 - H317 - H319

Classi di pericolo

Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1B

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

165.2 °F - closed cup

Punto d’infiammabilità (°C)

74 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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Citral natural, ≥96%, FCC, FG

Sigma-Aldrich

W230316

Citral

Citronellol mixture of isomers, natural, ≥95%, FG

Sigma-Aldrich

W230915

Citronellol

(±)-β-Citronellol analytical standard

Supelco

51381

(±)-β-Citronellol

Citronellyl acetate ≥95%, FCC, FG

Sigma-Aldrich

W231118

Citronellyl acetate

Hajo Kries et al.
The Journal of biological chemistry, 292(35), 14659-14667 (2017-07-14)
The natural product class of iridoids, found in various species of flowering plants, harbors astonishing chemical complexity. The discovery of iridoid biosynthetic genes in the medicinal plant Catharanthus roseus has provided insight into the biosynthetic origins of this class of
Raimundo Wagner de S Aguiar et al.
TheScientificWorldJournal, 2014, 492138-492138 (2014-03-07)
Corymbia citriodora and Cymbopogon nardus essential oils samples were analyzed by GC and GC-MS and their qualitative and quantitative compositions established. The main component of essential oils of C. citriodora and C. nardus was citronellal, at 61.78% and 36.6%, respectively.
Walter S Leal et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(46), 18704-18709 (2013-10-30)
The southern house mosquito, Culex quinquefasciatus, has one of the most acute and eclectic olfactory systems of all mosquito species hitherto studied. Here, we used Illumina sequencing to identify olfactory genes expressed predominantly in antenna, mosquito's main olfactory organ. Less
Lucindo José Quintans-Júnior et al.
Journal of orofacial pain, 24(3), 305-312 (2010-07-29)
To evaluate the antinociceptive effects of citronellal (CTL) on formalin-, capsaicin-, and glutamate-induced orofacial nociception in mice and to investigate whether such effects might involve a change in neural excitability. Male mice were pretreated with CTL (50, 100, and 200
Ying-Fang Ting et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 16(23), 7030-7038 (2010-05-11)
Practical and convenient synthetic routes have been developed for the synthesis of a new class of pyrrolidinyl-camphor derivatives (7 a-h). These novel compounds were screened as catalysts for the direct Michael addition of symmetrical alpha,alpha-disubstituted aldehydes to beta-nitroalkenes. When this
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