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2-methyl decanal (aldehyde C-11 MOA)

Chemical Structure

General Material Information

Preferred name 2-methyl decanal (aldehyde C-11 MOA)
Trivial Name 2-Methyldecanal
Short Description aldehyde MOA
Formula C11 H22 O
CAS Number 19009-56-4
Deleted CAS Number 120892-77-5
Flavis Number 5.16
ECHA Number 242-745-6
FDA UNII Search
Nikkaji Number J34.879A
Beilstein Number 1753165
xLogP3-AA 4.40 (est)
Bio Activity Summary External link
NMR Predictor External link
Synonyms
  • aldehyde C-11 moa
  • aldehyde C11 MOA
  • aldehyde MOA
  • decanal, 2-methyl-
  • 1-decanal, 2-methyl-
  • 2-methyl decan-1-al
  • 2-methyl decanal
  • 2-methyl decanal (aldehyde C-11 MOA)
  • methyl octyl acetaldehyde
  • 2-methyl-1-decanal
  • 2-methyl-decanal
  • 2-methyldecan-1-al
  • 2-methyldecanal
  • methyloctylacetaldehyde
  • 2-Methyldecanal
  • α-Methyldecanal

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Literature & References

2-methyldecanal
NIST Chemistry WebBook:Search Inchi
Canada Domestic Sub. List:19009-56-4
Pubchem (cid):29381
Pubchem (sid):134992523
Publications by PubMed
Comparison of the volatile oil composition of three Atalantia species.
The effect of feed solids concentration and inlet temperature on the flavor of spray dried whey protein concentrate.
Abelmoschus esculentus (L.) Moench. and Abelmoschus moschatus Medik: seeds production and analysis of the volatile compounds.
Apple volatiles synergize the response of codling moth to pear ester.
Effect of storage time and heat processing on the volatile profile of Senegalese sole (Solea senegalensis Kaup, 1858) muscle.
Influence of processing on the volatile profile of strawberry spreads made with isomaltulose.
Aroma volatile compounds from two fresh pineapple varieties in china.
[Diurnal rhythm of Viburnum awabuki and Betula luminifera volatiles and electroantennogram response of Batocera horsfieldi].
Hot and cold water infusion aroma profiles of Hibiscus sabdariffa: fresh compared with dried.
Influence of pulsed electric field treatments on the volatile compounds of milk in comparison with pasteurized processing.
Behavioral responses of the leafhopper, Cicadulina storeyi China, a major vector of maize streak virus, to volatile cues from intact and leafhopper-damaged maize.
Electrophysiological and behavioral responses of sorghum shoot fly, Atherigona soccata, to sorghum volatiles.
An evaluation of volatile compounds released from containers commonly used in circulation of sports beverages.
Arm-in-cage testing of natural human-derived mosquito repellents.
Prolonged stimulus exposure reveals prolonged neurobehavioral response patterns.
Influence of growth phase and geographic origin on the essential oil composition of Pituranthos chloranthus from Tunisia.
Between plant and diurnal variation in quantities and ratios of volatile compounds emitted by Vicia faba plants.
Identification of volatile compounds used in host location by the black bean aphid, Aphis fabae.
Ozone-initiated chemistry in an occupied simulated aircraft cabin.
Gas chromatographic/mass spectrometric analysis of the essential oil of Houttuynia cordata Thunb by using on-column methylation with tetramethylammonium acetate.
Volatile emissions from Aesculus hippocastanum induced by mining of larval stages of Cameraria ohridella influence oviposition by conspecific females.
Comparative analysis of volatile constituents from mice and their urine.
Characterization of volatile compounds in chilled cod (Gadus morhua) fillets by gas chromatography and detection of quality indicators by an electronic nose.
Volatile constituents of redblush grapefruit (Citrus paradisi) and pummelo (Citrus grandis) peel essential oils from Kenya.
Aroma composition of red wines by different extraction methods and Gas Chromatography-SIM/MASS spectrometry analysis.
Products and mechanism of the reaction of OH radicals with 2,3,4-trimethylpentane in the presence of NO.
Production of volatile compounds by Fuji apples following exposure to high CO2 or low O2.
Sampling and analysis of volatile organic compounds in bovine breath by solid-phase microextraction and gas chromatography-mass spectrometry.
Identification of odoriferous compounds from adults of a swallowtail butterfly, Papilio machaon (Lepidoptera: Papilionidae).
Aroma of fresh oysters Crassostrea gigas: composition and aroma notes.
Reductions with lithium in low molecular weight amines and ethylenediamine
Identification of impact odorants in Bordeaux red grape juice, in the commercial yeast used for its fermentation, and in the produced wine.
Chemicals in laboratory room air stimulate olfactory neurons of female Bombyx mori.
Identification of electrophysiologically-active compounds for the malaria mosquito, Anopheles gambiae, in human sweat extracts.
Selective odor perception in the soil collembolaOnychiurus armatus.
Nonquaternary cholinesterase reactivators. 3. 3(5)-Substituted 1,2,4-oxadiazol-5(3)-aldoximes and 1,2,4-oxadiazole-5(3)-thiocarbohydroximates as reactivators of organophosphonate-inhibited eel and human acetylcholinesterase in vitro.

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
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2912.30.0000
ChemSpider:View
Wikipedia:View

PhysChem Properties

Material listed in food chemical codex No
Molecular weight 170.29554748535
Specific gravity @ 25 °C
Pounds per Gallon 6.748 to 6.881
Specific gravity @ 20 °C
Pounds per Gallon 6.84 to 6.906
Refractive Index 1.425 to 1.435 @ 20 °C
Acid Value 10 max KOH/g
Vapor Pressure 0.102 mmHg @ 25 °C
Flash Point TCC Value 81.11 °C TCC
logP (o/w) 4.324 est
Solubility
alcohol Yes
water, 16.49 mg/L @ 25 °C (est) Yes
water No
Stability
alkali mild Unspecified
antiperspirant Unspecified
deodorant Unspecified

Organoleptic Properties

Odor Type: Citrus
fresh, dry, citrus, waxy, watery
Odor strength high , recommend smelling in a 1.00 % solution or less
Substantivity 172 hour(s) at 100.00 %
Luebke, William tgsc, (1985) At 1.00 % in dipropylene glycol. powerful fresh dry citrus waxy watery
Flavor Type: Citrus
citrus, aldehydic, fatty, herbal, waxy, citrus rind, soapy, incense
Luebke, William tgsc, (1985) Citrus aldehydic fatty herbal waxy citrus rind soapy incense
General comment Citrus, aldehydic, fatty, on dilution herbal-incense note

Potential Uses

Applications
Odor purposes Aldehydic, Amber, Chypre, Citrus, Fern, Fresh and clean, Herbal
Other purposes Clean, Watery, Waxy
Cosmetic purposes Perfuming agents

Safety Information

Safety information

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.
Human Experience:
10 % solution: no irritation or sensitization.
Oral/Parenteral Toxicity:
oral-rat LD50 > 5000 mg/kg
(Moreno, 1975p)

oral-rat LD50 > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 14, Pg. 609, 1976.

Dermal Toxicity:
skin-rabbit LD50 > 5000 mg/kg
Food and Cosmetics Toxicology. Vol. 14, Pg. 609, 1976.

Inhalation Toxicity:
Not determined

Safety in use information

Category:
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
Recommendation for 2-methyl decanal (aldehyde C-11 MOA) usage levels up to:
1.0000 % in the fragrance concentrate.
Maximised Survey-derived Daily Intakes (MSDI-EU): 0.011 (μg/capita/day)
Modified Theoretical Added Maximum Daily Intake (mTAMDI): 1000 (μg/person/day)
Threshold of Concern:1800 (μg/person/day)
Structure Class: I
Food categories according to Commission Regulation EC No. 1565/2000 (EC, 2000) in FGE.06 (EFSA, 2002a). According to the Industry the "normal" use is defined as the average of reported usages and "maximum use" is defined as the 95th percentile of reported usages (EFSA, 2002i).
Note: mg/kg = 0.001/1000 = 0.000001 = 1/1000000 = ppm.
average usage mg/kgmaximum usage mg/kg
Dairy products, excluding products of category 02.0 (01.0): 3.0000015.00000
Fats and oils, and fat emulsions (type water-in-oil) (02.0): 2.0000010.00000
Edible ices, including sherbet and sorbet (03.0): 3.0000015.00000
Processed fruit (04.1): 2.0000010.00000
Processed vegetables (incl. mushrooms & fungi, roots & tubers, pulses and legumes), and nuts & seeds (04.2): --
Confectionery (05.0): 4.0000020.00000
Chewing gum (05.3): --
Cereals and cereal products, incl. flours & starches from roots & tubers, pulses & legumes, excluding bakery (06.0): 2.0000010.00000
Bakery wares (07.0): 5.0000025.00000
Meat and meat products, including poultry and game (08.0): 1.000005.00000
Fish and fish products, including molluscs, crustaceans and echinoderms (MCE) (09.0): 1.000005.00000
Eggs and egg products (10.0): --
Sweeteners, including honey (11.0): --
Salts, spices, soups, sauces, salads, protein products, etc. (12.0): 2.0000010.00000
Foodstuffs intended for particular nutritional uses (13.0): 3.0000015.00000
Non-alcoholic ("soft") beverages, excl. dairy products (14.1): --
Alcoholic beverages, incl. alcohol-free and low-alcoholic counterparts (14.2): 4.0000020.00000
Ready-to-eat savouries (15.0): 5.0000025.00000
Composite foods (e.g. casseroles, meat pies, mincemeat) - foods that could not be placed in categories 01.0 - 15.0 (16.0): 2.0000010.00000

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):

Flavouring Group Evaluation 1, Revision 1 (FGE.01Rev 1): Branched-chain aliphatic saturated aldehydes, carboxylic acids and related esters of primary alcohols and branched-chain carboxylic acids from chemical groups 1 and 2 (Commission Regulation (EC) No 1565/2000 of 18 July 2000) - Scientific Opinion of the Panel on Food Additives, Flavourings, Processing Aids and Materials in contact with Food (AFC) on a request from the Commission
View page or View pdf

Flavouring Group Evaluation 01 Rev2 (FGE.01 Rev2): Branched-chain aliphatic saturated aldehydes, carboxylic acids and related esters of primary alcohols and branched-chain carboxylic acids from chemical groups 1 and 2
View page or View pdf

EPI System: View
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):19009-56-4
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :29381
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:2
2-methyldecanal
Chemidplus:0019009564