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2-Undecanone

2-Undecanone Structure
CAS No.
112-12-9
Chemical Name:
2-Undecanone
Synonyms
METHYL NONYL KETONE;Undecan-2-one;FEMA 3093;undecan-2-;2-Undecanon;Undecan-2-on;2-UNDECANONE;2-hendecanone;Undecanone-(2);2-eleven ketone
CBNumber:
CB5285835
Molecular Formula:
C11H22O
Molecular Weight:
170.29
MOL File:
112-12-9.mol
MSDS File:
SDS
Modify Date:
2025/1/27 9:38:02

2-Undecanone Properties

Melting point 11-13 °C(lit.)
Boiling point 231-232 °C(lit.)
Density 0.825 g/mL at 25 °C(lit.)
vapor density 5.9 (vs air)
vapor pressure <1 mm Hg ( 20 °C)
refractive index n20/D 1.43(lit.)
FEMA 3093 | 2-UNDECANONE
Flash point 192 °F
storage temp. Store below +30°C.
form Liquid
color Clear colorless to light yellow
Odor at 100.00 %. waxy fruity creamy fatty orris floral
Odor Type fruity
biological source synthetic
Water Solubility INSOLUBLE
Merck 14,6104
JECFA Number 296
BRN 1749573
Dielectric constant 8.4000000000000004
Stability Stable. Combustible. Incompatible with strong oxidizing agents, strong bases.
LogP 3.69 at 25℃
CAS DataBase Reference 112-12-9(CAS DataBase Reference)
NIST Chemistry Reference 2-Undecanone(112-12-9)
EPA Substance Registry System Methyl nonyl ketone (112-12-9)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS09
Signal word  Warning
Hazard statements  H410
Precautionary statements  P273-P391-P501
Hazard Codes  N
Risk Statements  51/53-50/53
Safety Statements  23-24/25-61-60
RIDADR  UN3082
WGK Germany  2
RTECS  YQ2820000
TSCA  Yes
HazardClass  9
PackingGroup  III
HS Code  29141990
Hazardous Substances Data 112-12-9(Hazardous Substances Data)
Toxicity LD50 dermally in rabbits: >5 g/kg; LD50 orally in rats, mice: >5, 3.88 g/kg (Opdyke)
NFPA 704
2
1 0

2-Undecanone price More Price(17)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) W309311 2-Undecanone natural, FCC, FG 112-12-9 1SAMPLE-K ₹5347.55 2022-06-14 Buy
Sigma-Aldrich(India) W309303 2-Undecanone ≥98%, FCC, FG 112-12-9 1SAMPLE-K ₹5141.88 2022-06-14 Buy
Sigma-Aldrich(India) W309311 2-Undecanone natural, FCC, FG 112-12-9 100G ₹20762.35 2022-06-14 Buy
Sigma-Aldrich(India) W309303 2-Undecanone ≥98%, FCC, FG 112-12-9 250G ₹8053.8 2022-06-14 Buy
Sigma-Aldrich(India) W309311 2-Undecanone natural, FCC, FG 112-12-9 1KG ₹105532.93 2022-06-14 Buy
Product number Packaging Price Buy
W309311 1SAMPLE-K ₹5347.55 Buy
W309303 1SAMPLE-K ₹5141.88 Buy
W309311 100G ₹20762.35 Buy
W309303 250G ₹8053.8 Buy
W309311 1KG ₹105532.93 Buy

2-Undecanone Chemical Properties,Uses,Production

Chemical Properties

2-undecanone, also known as methyl nonyl ketone, is a colorless to slightly yellow liquid and has a characteristic rue odor with a sweet flavor reminiscent of peach (on dilution). It naturally exists in Houttuynia cordata, bananas, strawberries, cloves, ginger and Rutaceae plants. The FEMA number is 3093, the FDA number is 172.515, and the CoE number is 150. methyl nonyl ketone is the active ingredient of Houttuynia cordata, mainly used in the production of medicines and fragrances, and is safer and more effective than DEET for mosquito repellents.

Physical properties

Methyl nonyl ketone (MNK) is a clear mobile liquid, with a strong characteristic smell at room temperature that presents a vapour pressure of 11.8 Pascals at 20° C. It has a very low solubility in water and high solubility in organic solvents such as n-heptane, p-xylene, 1,2-dichloroethane, methanol, acetone and ethyl acetate. MNK is not considered highly flammable or explosive or oxidizing.

Occurrence

Originally reported found in the essential oils of Ruta graveolens; subsequently was identified in the essential oils of Citrus limetta Risso., Fagara xanthoxyloides Lamm. and Litsea odorifera Val. (leaves); a method for the determination of methyl nonyl ketone in various rue species (Ruta montana, Ruta bracteosa) was devised; it is also present in the essential oils of Jaborandi (leaves), Hottuynia cordata, Phellodendron anaurense, Schizandar nigra Maxim., and in coconut and palm oils; also identified as the main constituent of the essential oil of Boronia ledifolia Gai; a 92% content level was reported in the essential oil of Ruta chalepensis. Also reported found in rabbiteye, blueberry, feijoa fruit, feijoa peel, peach, raspberry, fresh black berry, heated blackberry, strawberry jam, guava, allium, cloves, raw asparagus, shallot, roasted onion, ginger, Curcuma aeruginosa Roxb., Curcuma heyneana Val., banana, grapefruit, currants, peach, asparagus, shallot, onion, leek, chive, peas, potato, clove, ginger, pepper, many cheeses, wheaten bread, butter, milk, cream, yogurt, milk powder, goat and sheep milk, caviar, raw and smoked fatty fish, roast chicken, cooked beef, beef, chicken and pork fat, hop oil, beer, cognac, rum, sparkling wine, coffee, tea, roasted filberts and peanuts, coconut meat, milk and oil, passion fruit, mushroom, wild marjoram, starfruit, Brazil nut, cardamom, rice, buckwheat, corn oil, wort, elder flower, shrimp, crayfish, clam, maté and mastic gum leaf and fruit oil.

Uses

2-Undecanone may be used as an analytical reference standard for the quantification of the analyte in milk samples and Houttuynia cordata Thunb using gas chromatography (GC) technique.

Preparation

Can be isolated from natural oils by fractional distillation; also by dry distillation of calcium acetate and calcium caprylate, or by boiling octylacetoacetic acid ethyl ester with and alcoholic KOH solution.

Definition

ChEBI: 2-Undecanone is a dialkyl ketone with methyl and nonyl as the two alkyl groups. It has a role as a rodenticide and a plant metabolite. It is a dialkyl ketone and a methyl ketone.

General Description

2-Undecanone is a naturally available nontoxic insect repellant, introduced as an alternative to insect repellants containing N,N-diethyl-meta-toluamide. It is isolated from the trichomes of wild tomatoes 2-Undecanone is also a volatile constituent, identified in milk and Houttuynia cordata Thunb?(HCT), a traditional Chinese medicine.

Safety Profile

Moderately toxic by ingestion. Combustible when exposed to heat or flame; can react with oxidizing materials. To fight fLt-e, use CO2, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes. See also KETONES.

Synthesis

2-Undecanone's three synthesis methods is as follows:1) by oxidation of Undecanol-2.2) from Decanoic acid and Acetic acid, heated over Thorium oxide to 450℃.3) The isolation from Rue oil is of no commercial importance.

2-Undecanone Preparation Products And Raw materials

Global( 464)Suppliers
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Nagar Haveli Perfumes & Aromatics +917506551149 Mumbai, India 230 58 Inquiry
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TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6768 58 Inquiry
Hebei Mujin Biotechnology Co.,Ltd +86 13288715578 +8613288715578 China 12831 58 Inquiry
FEMA 3093 METHYL N-NONYL KETONE UNDECANAL 96+% FCC 2-UNDECANONE, 1GM, NEAT 2-UNDECANONE 98+% FCC 2-UNDECANONE OEKANAL Methyl-n-nonylketone,95% 2-Undecanone, 97.50% undecanone,2-undecanone METHYLNONYLKETON REIN Undecan-2-on 2-UNDECANONE 2-hendecanone Undecanone-(2) 2-UNDECANONE, 99% NATURAL 2-UNDECANONE 98+% METHYLNONYLKETONE WITH GC METHYL NONYL KETONE, NATURAL Undecanone, 2-: (Methyl nonyl ketone) 2-eleven ketone 2-Undecanone, 98% 250ML 2-Undecanon Ketone, methyl nonyl Methyl-nonylketon Mgk dog & cat repellent Mgk dog and cat repellent mgkdogandcatrepellent Nonyl methyl ketone nonylmethylketone undecan-2- 2-UNDECANONE FOR SYNTHESIS 500 ML 2-UNDECANONE FOR SYNTHESIS 20 KG 2-UNDECANONE FOR SYNTHESIS 100 ML METHYL NONYL KETONE FCC Methyl n-nonone Undecan-2-one (Methyl-nonyl-ketone)@100 μg/mL in Acetonitrile Methyl nonyl ketone@100 μg/mL in AcCN Undecanone Undecanone Methyl nonyl ketone@100 μg/mL in Methanol 2-Undecanone USP/EP/BP METHYL NONYL KETONE Undecan-2-one Racecadotril Impurity 20 2-Undecanone Solution in Methanol/Water(90:10) C17896600 2-Undecanone Sodium caprylate EP Impurity I 2-Undecanone, 10 mM in DMSO 112-12-9 0112-12-09 CH3CH28COCH3 112129 C9H19COCH3 Building Blocks C11 to C12 Carbonyl Compounds Ketones Organic Building Blocks Building Blocks