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General Material Information

Preferred name perillaldehyde
Trivial Name Perillaldehyde
Short Description p-mentha-1,8-dien-7-al
Formula C10 H14 O
CAS Number 2111-75-3
Deleted CAS Number 1254961-45-9
FEMA Number 3557
Flavis Number 5.117
ECHA Number 218-302-8
FDA UNII 6EQL0XA86G
Nikkaji Number J2.142C
MDL MFCD00001543
COE Number 11788
xLogP3-AA 2.60 (est)
Bio Activity Summary External link
NMR Predictor External link
JECFA Food Flavoring 973 p-mentha-1,8-dien-7-al
FDA Patent No longer provide for the use of these seven synthetic flavoring substances
FDA Mainterm 2111-75-3 ; PERILLALDEHYDE
Synonyms
  • 1-cyclohexene-1-carboxaldehyde, 4-(1-methylethenyl)-
  • 1-cyclohexene-1-carboxaldehyde, 4-isopropenyl-
  • dihydro cuminyl aldehyde
  • dihydro cuminyl aldehyde natural
  • dihydrocuminic aldehyde
  • dihydrocuminyl aldehyde
  • dihydrocuminylaldehyde
  • p- mentha-1,8-dien-7-al
  • para- mentha-1,8-dien-7-al
  • 1,8-p- menthadien-7-al
  • 4-(1-methyl ethenyl)-1-cyclohexene-1-carboxaldehyde
  • 4-(1-methylethenyl)-1-cyclohexene-1-carboxaldehyde
  • 4-(1-methylethenyl)-1-cyclohexene1-carboxyaldehyde
  • perilla aldehyde
  • perilla aldehyde natural
  • perillaaldehyde
  • perillal
  • DL- perillaldehyde
  • perillic aldehyde
  • perillyl aldehyde
  • perillylaldehyde
  • 4-( prop-1-en-2-yl)cyclohex-1-ene-1-carbaldehyde
  • 4-prop-1-en-2-ylcyclohexene-1-carbaldehyde
  • 4-iso propenyl cyclohex-1-ene carbaldehyde
  • 4-iso propenyl-1-cyclohexene-1-carbaldehyde
  • 4-iso propenyl-1-cyclohexene-1-carboxaldehyde
  • 4-iso propenylcyclohex-1-enecarbaldehyde
  • 4-prop-1-en-2-ylcyclohexene-1-carbaldehyde
  • 1-Cyclohexene-1-carboxaldehyde, 4-(1-methylethenyl)-
  • 1-Cyclohexene-1-carboxaldehyde, 4-isopropenyl-
  • 4-(1-Methylethenyl)-1-cyclohexene-1-carboxaldehyde
  • 4-Isopropenyl-1-cyclohexene-1-carboxaldehyde
  • p-Mentha-1,8-dien-7-al
  • 4-Isopropenyl-1-cyclohexenecarboxaldehyde
  • 4-(2-Propenyl)-1-cyclohexenecarboxaldehyde
  • (±)-Perillaldehyde
  • dl-Perillaldehyde
  • NSC 138642
  • 1,8-p-Menthadien-7-al
  • 4-(Prop-1-en-2-yl)cyclohex-1-ene-1-carboxaldehyde
  • Para-menth-1,8-dien-7-al

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Literature & References

4-prop-1-en-2-ylcyclohexene-1-carbaldehyde
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:2111-75-3
Pubchem (cid):16441
Pubchem (sid):134982357
Flavornet:2111-75-3
Pherobase:View
Publications by PubMed
Antimicrobial activity of Ammodaucus leucotrichus fruit oil from Algerian Sahara.
Fumigant activity of eleven essential oil compounds and their selected binary mixtures against Culex pipiens pallens (Diptera: Culicidae).
Two types of alcohol dehydrogenase from Perilla can form citral and perillaldehyde.
Synthesis and antiproliferative effects of amino-modified perillyl alcohol derivatives.
Chemical composition and mosquito repellency of essential oil of Conyza newii propagated in different geographical locations of Kenya.
Effects of perillaldehyde on alternations in serum cytokines and depressive-like behavior in mice after lipopolysaccharide administration.
Dominant colonization and inheritance of Methylobacterium sp. strain OR01 on perilla plants.
Concise total synthesis of spirocurcasone.
Efficient preparation of Hangekobokuto (Banxia-Houpo-Tang) decoction by adding perilla herb before decoction is finished.
Whole-cell-based CYP153A6-catalyzed (S)-limonene hydroxylation efficiency depends on host background and profits from monoterpene uptake via AlkL.
Enhancing antioxidant capacity and reducing decay of chinese bayberries by essential oils.
Influence of the active compounds of Perilla frutescens leaves on lipid membranes.
Antibacterial activity of the essential oil and main components of two Dracocephalum species from Iran.
Development of quality assessment method for optically active food flavor chemicals.
Bioreduction of α,β-unsaturated ketones and aldehydes by non-conventional yeast (NCY) whole-cells.
(S)-Perillaldehyde azine.
Inhibitory activity of hydrosols, herbal teas and related essential oils against filament formation and the growth of Candida albicans.
Chemical composition and antimicrobial activity of the extracts of Kefe cumin (Laser trilobum L.) fruits from different regions.
Preliminary analysis on essential oil composition of Perilla L. cultivated in Lithuania.
A nine-step total synthesis of (-)-platencin.
Site-saturation mutagenesis of tryptophan 116 of Saccharomyces pastorianus old yellow enzyme uncovers stereocomplementary variants.
Taste-guided identification of high potency TRPA1 agonists from Perilla frutescens.
Fragrant unsaturated aldehydes elicit activation of the Keap1/Nrf2 system leading to the upregulation of thioredoxin expression and protection against oxidative stress.
Antidepressant-like Effect of l-perillaldehyde in Stress-induced Depression-like Model Mice through Regulation of the Olfactory Nervous System.
Conformational flexibility in terpenes: vibrational circular dichroism (VCD), infrared and Raman study of S-(-)-perillaldehyde.
The monoterpenoids citral and geraniol are moderate inhibitors of CYP2B6 hydroxylase activity.
Opposite stereochemical courses for enzyme-mediated alkene reductions of an enantiomeric substrate pair.
Increasing antioxidant activity and reducing decay of blueberries by essential oils.
Influence of cinnamon and clove essential oils on the D- and z-values of Escherichia coli O157:H7 in apple cider.
Parectadial, a monoterpenoid from the defensive spray of Parectatosoma mocquerysi.
Synthesis and biological activity of novel pyranopyrones derived from engineered aromatic polyketides.
Biotransformation of terpenoids by mammals, microorganisms, and plant-cultured cells.
Antimicrobial effect of trans-cinnamaldehyde, (-)-perillaldehyde, (-)-citronellal, citral, eugenol and carvacrol on airborne microbes using an airwasher.
Analysis by gas chromatography-mass spectrometry of the volatiles from the fruits of Ammodaucus leucotrichus subsp. leucotrichus and subsp. nanocarpus grown in North Africa and the Canary Islands, respectively.
Vasodilative effect of perillaldehyde on isolated rat aorta.
Fumigant toxicity of the essential oils of some African plants against Anopheles gambiae sensu stricto.
Repellency of essential oils of some Kenyan plants against Anopheles gambiae.
Antibacterial activities of naturally occurring compounds against antibiotic-resistant Bacillus cereus vegetative cells and spores, Escherichia coli, and Staphylococcus aureus.
Essential oils: their antibacterial properties and potential applications in foods--a review.
Study of the carbonyl products of terpene/OH radical reactions: detection of the 2,4-DNPH derivatives by HPLC-MS.
Action of different monoterpenic compounds against Anisakis simplex s.l. L3 larvae.
Perillyl alcohol and perillaldehyde induced cell cycle arrest and cell death in BroTo and A549 cells cultured in vitro.
Synthesis of both enantiomers of isorobinal, a novel cyclic monoterpene isolated from the astigmatid mite, Rhizoglyphus sp.
Bactericidal activities of plant essential oils and some of their isolated constituents against Campylobacter jejuni, Escherichia coli, Listeria monocytogenes, and Salmonella enterica.
Carvone and perillaldehyde interfere with the serum-induced formation of filamentous structures in Candida albicans at substantially lower concentrations than those causing significant inhibition of growth.
Cytotoxicity and biotransformation of the anticancer drug perillyl alcohol in PC12 cells and in the rat.
Effects of branched cyclodextrins on the solubility and stability of terpenes.
Quantification of carvone, cineole, perillaldehyde, perillyl alcohol and sobrerol by isocratic high-performance liquid chromatography.
Insecticidal activity of monoterpenoids to western corn rootworm (Coleoptera: Chrysomelidae), twospotted spider mite (Acari: Tetranychidae), and house fly (Diptera: Muscidae).
Isoprenoids suppress the growth of murine B16 melanomas in vitro and in vivo.
cDNA cloning, characterization, and functional expression of 4S-(-)-limonene synthase from Perilla frutescens.
Genetic analysis of essential oil variants in Perilla frutescens.
Absolute configuration of a new mosquito repellent, (+)-eucamalol and the repellent activity of its epimer.
[Constituents of essential oils from leaves, stems, and fruits of Perilla frutescens (L.) Britt].
Olfactory sensitivity of two sympatric species of rice leaf folders (Lepidoptera: Pyralidae) to plant volatiles.
Hepatic microsomal oxygenation of aldehydes to carboxylic acids.
Terpenoid biotransformation in mammals. V. Metabolism of (+)-citronellal, (+-)-7-hydroxycitronellal, citral, (-)-perillaldehyde, (-)-myrtenal, cuminaldehyde, thujone, and (+-)-carvone in rabbits.
[Pharmacological studies on Perillae Herba. I. Neuropharmacological action of water extract and perillaldehyde (author's transl)].

Other Information

(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
FDA Substances Added to Food (formerly EAFUS):View
CHEBI:View
CHEMBL:View
Golm Metabolome Database:Search
UM BBD:Search
KEGG (GenomeNet):C02576
HMDB (The Human Metabolome Database):HMDB03647
FooDB:FDB014789
Export Tariff Code:2912.49.0000
Typical G.C.
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
Wikipedia:View

PhysChem Properties

Material listed in food chemical codex No
Molecular weight 150.22077941895
Specific gravity @ 25 °C
Pounds per Gallon 7.822 to 7.955
Refractive Index 1.504 to 1.513 @ 20 °C
Optical Rotation -125 to -118
Boiling Point 238 to 240°C @ 760 mm Hg
Vapor Pressure 0.043 mmHg @ 25 °C
Flash Point TCC Value 93.33 °C TCC
logP (o/w) 3.053 est
Solubility
alcohol Yes
oils Yes
water, 160.7 mg/L @ 25 °C (est) Yes
water No

Organoleptic Properties

Odor Type: Herbal
fresh, green, herbal, grassy, sweet, minty, cumin, spicy, citrus, cinnamon, pungent, clove, orange, lime
Odor strength high , recommend smelling in a 10.00 % solution or less
Substantivity 8 hour(s) at 100.00 %
Luebke, William tgsc, (1986) At 10.00 % in dipropylene glycol. fresh green herbal grassy sweet mint cumin spicy citrus
Mosciano, Gerard P&F 22, No. 5, 67, (1997) Spicy, cumin, cinnamon, pungent, clove, citrus, orange and lime
Flavor Type: Spicy
aromatic, woody, spicy, waxy, cinnamyl, orange, lime, sweet, citrus, aldehydic
Luebke, William tgsc, (1986) Aromatic sweet woody spicy waxy aldehydic cinnamyl orange lime
Mosciano, Gerard P&F 22, No. 5, 67, (1997) At 25.00 ppm. Woody, spicy, waxy, sweet, citrus, lime and aldehydic

Occurrences

Safety Information

Safety information

European information :
Most important hazard(s):
Xi - Irritant
R 36/37/38 - Irritating to eyes, respiratory system, and skin.
S 02 - Keep out of the reach of children.
S 24/25 - Avoid contact with skin and eyes.
S 26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
S 37/39 - Wear suitable gloves and eye/face protection.
Hazards identification
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
Pictogram
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
oral-mouse LD50 1720 mg/kg
Food and Chemical Toxicology. Vol. 20, Pg. 799, 1982.

Dermal Toxicity:
skin-guinea pig LD50 > 5000 mg/kg
Food and Chemical Toxicology. Vol. 20, Pg. 799, 1982.

Inhalation Toxicity:
Not determined

Safety in use information

Category:
cosmetic, flavor and fragrance agents
RIFM Fragrance Material Safety Assessment: Search
IFRA Code of Practice Notification of the 49th Amendment to the IFRA Code of Practice
IFRA Critical Effect:
Dermal sensitization
IFRA fragrance material specification:
Should not be used such that the level in finished cosmetic products exceeds 0.1%. Based on test results showing sensitisation (IFRA guidelines).
View the IFRA Standard
View IFRA Standards Library for complete information.
Please review Amendment 49 IFRA documentation for complete information.
IFRA RESTRICTION LIMITS IN THE FINISHED PRODUCT (%):
Category 1: Products applied to the lips
0.054 %
Category 2: Products applied to the axillae
0.016 %
Category 3: Products applied to the face/body using fingertips
0.32 %
Category 4: Products related to fine fragrance
0.30 %
Category 5: Products applied to the face and body using the hands (palms), primarily leave-on
Category 5A: Body lotion products applied to the body using the hands (palms), primarily leave-on
0.076 %
Category 5B: Face moisturizer products applied to the face using the hands (palms), primarily leave-on
0.076 %
Category 5C: Hand cream products applied to the hands using the hands (palms), primarily leave-on
0.076 %
Category 5D: Baby Creams, baby Oils and baby talc
0.076 %
Category 6: Products with oral and lip exposure
0.18 %
Category 7: Products applied to the hair with some hand contact
Category 7A: Rinse-off products applied to the hair with some hand contact
0.61 %
Category 7B: Leave-on products applied to the hair with some hand contact
0.61 %
Category 8: Products with significant anogenital exposure
0.032 %
Category 9: Products with body and hand exposure, primarily rinse off
0.59 %
Category 10: Household care products with mostly hand contact
Category 10A: Household care excluding aerosol products (excluding aerosol/spray products)
2.10 %
Category 10B: Household aerosol/spray products
2.10 %
Category 11: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate
Category 11A: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate without UV exposure
1.20 %
Category 11B: Products with intended skin contact but minimal transfer of fragrance to skin from inert substrate with potential UV exposure
1.20 %
Category 12: Products not intended for direct skin contact, minimal or insignificant transfer to skin
No Restriction
Notes:
IFRA FLAVOR REQUIREMENTS:

Due to the possible ingestion of small amounts of fragrance ingredients from their use in products in Categories 1 and 6, materials must not only comply with IFRA Standards but must also be recognized as safe as a flavoring ingredient as defined by the IOFI Code of Practice (www.iofi.org). For more details see chapter 1 of the Guidance for the use of IFRA Standards.

Maximised Survey-derived Daily Intakes (MSDI-EU): 2.10 (μg/capita/day)
Maximised Survey-derived Daily Intakes (MSDI-USA): 2.00 (μg/capita/day)
Structure Class: I
Use levels for FEMA GRAS flavoring substances on which the FEMA Expert Panel based its judgments that the substances are generally recognized as safe (GRAS).
The Expert Panel also publishes separate extensive reviews of scientific information on all FEMA GRAS flavoring substances and can be found at FEMA Flavor Ingredient Library
publication number: 11
Click here to view publication 11
average usual ppmaverage maximum ppm
baked goods: -4.50000
beverages(nonalcoholic): -4.00000
beverages(alcoholic): -6.00000
breakfast cereal: --
cheese: --
chewing gum: --
condiments / relishes: --
confectionery froastings: --
egg products: --
fats / oils: --
fish products: --
frozen dairy: -6.30000
fruit ices: --
gelatins / puddings: -4.50000
granulated sugar: --
gravies: --
hard candy: --
imitation dairy: --
instant coffee / tea: --
jams / jellies: --
meat products: -20.00000
milk products: --
nut products: --
other grains: --
poultry: --
processed fruits: --
processed vegetables: --
reconstituted vegetables: --
seasonings / flavors: --
snack foods: --
soft candy: -9.70000
soups: --
sugar substitutes: --
sweet sauces: --

Safety references

European Food Safety Athority(EFSA):Flavor usage levels; Subacute, Subchronic, Chronic and Carcinogenicity Studies; Developmental / Reproductive Toxicity Studies; Genotoxicity Studies...

European Food Safety Authority (EFSA) reference(s):

List of apha, beta-Unsaturated Aldehydes and Ketones representative of FGE.19 substances for Genotoxicity Testing [1] - Statement of the Panel on Food Contact Materials, Enzymes, Flavourings and Processing Aids (CEF)
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 208 Revision 1 (FGE.208Rev1): Consideration of genotoxicity data on representatives for 10 alicyclic aldehydes with the a,ß-unsaturation in ring / side-chain and precursors from chemical subgroup 2.2 of
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 208 Revision 2 (FGE.208Rev2): Consideration of genotoxicity data on alicyclic aldehydes with a,ß-unsaturation in ring/side-chain and precursors from chemical subgroup 2.2 of FGE.19
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 208 Revision 2 (FGE.208Rev2): Consideration of genotoxicity data on alicyclic aldehydes with a,ß-unsaturation in ring/side-chain and precursors from chemical subgroup 2.2 of FGE.19
View page or View pdf

Scientific Opinion on Flavouring Group Evaluation 208 Revision 3 (FGE.208Rev3): consideration of genotoxicity data on alicyclic aldehydes with a,ß-unsaturation in ring/side-chain and precursors from chemical subgroup 2.2 of FGE.19
View page or View pdf

EPI System: View
Chemical Carcinogenesis Research Information System:Search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):2111-75-3
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :16441
National Institute of Allergy and Infectious Diseases:Data
SCCNFP:opinion
WGK Germany:3
4-prop-1-en-2-ylcyclohexene-1-carbaldehyde
Chemidplus:0002111753