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W338907

Sigma-Aldrich

Safranal

≥90%, stabilized

Synonyme(s) :

2,3-Dihydro-2,2,6-trimethylbenzaldehyde

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About This Item

Formule empirique (notation de Hill):
C10H14O
Numéro CAS:
Poids moléculaire :
150.22
Numéro FEMA:
3389
Numéro Beilstein :
1932918
Numéro CE :
Conseil de l'Europe Nº :
10383
Numéro MDL:
Code UNSPSC :
12164502
ID de substance PubChem :
Numéro Flavis :
5.104
Nomenclature NACRES :
NA.21

Source biologique

synthetic

Niveau de qualité

Qualité

Halal
Kosher

Pureté

≥90%

Contient

α-tocopherol, synthetic as stabilizer

Indice de réfraction

n20/D 1.523 (lit.)

Point d'ébullition

70 °C/1 mmHg (lit.)

Densité

0.966 g/mL at 25 °C (lit.)

Application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

Allergène alimentaire

no known allergens

Propriétés organoleptiques

medicinal; herbaceous; woody; spicy; phenolic

Chaîne SMILES 

CC1=C(C=O)C(C)(C)CC=C1

InChI

1S/C10H14O/c1-8-5-4-6-10(2,3)9(8)7-11/h4-5,7H,6H2,1-3H3

Clé InChI

SGAWOGXMMPSZPB-UHFFFAOYSA-N

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Description générale

Safranal is the characteristic volatile aroma compound of saffron (Crocus Sativus L.).

Application


  • Proteomic and molecular analyses to understand the promotive effect of safranal on soybean growth under salt stress.: This study investigates the role of safranal in enhancing soybean growth under saline conditions through a proteomic and molecular lens, potentially offering insights into stress resistance mechanisms in crops (Kausar et al., 2024).

  • Investigation of the effect of safranal and crocin pre-treatment on hepatic injury induced by infrarenal aortic occlusion.: The study evaluates the protective effects of safranal and crocin on liver injury in an experimental model, highlighting their potential therapeutic benefits (Ozkececi et al., 2016).

Clause de non-responsabilité

For R&D or non-EU Food use. Not for retail sale.

Pictogrammes

Exclamation markEnvironment

Mention d'avertissement

Warning

Mentions de danger

Classification des risques

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1A

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

186.8 °F - closed cup

Point d'éclair (°C)

86 °C - closed cup

Équipement de protection individuelle

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


Certificats d'analyse (COA)

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Les clients ont également consulté

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Alireza Timcheh Hariri et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 48(10), 2803-2808 (2010-07-20)
In this study, the effects of crocin and safranal were studied against sub-acute toxicity of diazinon (DZN) on specific biomarkers, biochemical indices and enzymes levels in rats. Vitamin E (200 IU/kg), safranal at doses 0.025, 0.05 and 0.1 ml/kg and
Zheng Liu et al.
CNS neuroscience & therapeutics, 18(8), 623-630 (2012-05-29)
Safranal (2,6,6-trimethyl-1,3-cyclohexadiene-1-carboxaldehyde, C(10) H(14) O) is an active ingredient in the saffron, which is used in traditional medicine. It has been reported to have sedative and anti-epileptic effects, but its hypnotic effects remain uncertain. The aim of this study was
Mehdi Jalali-Heravi et al.
Analytica chimica acta, 662(2), 143-154 (2010-02-23)
Volatile components of saffron from different regions of Iran were extracted by ultrasonic-assisted solvent extraction (USE) and were analyzed by gas chromatography-mass spectrometry (GC-MS). Self-modeling curve resolution (SMCR) was proposed for resolving the co-eluted GC-MS peak clusters into pure chromatograms
Analysis of the volatile components of saffron.
Rodel W & Petrzika M.
Journal of Separation Science, 14(11), 771-774 (1991)
Syed Sarim Imam et al.
Materials science & engineering. C, Materials for biological applications, 75, 1198-1205 (2017-04-19)
The present study was designed to formulate and optimize transdermal risperidone soft lipid vesicles. The formulation optimized with phospholipid, safranal and ethanol were incorporated as permeation and absorption enhancers. The optimized risperidone soft lipid vesicle was further evaluated for skin

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