Basic information Background Chemical Properties Preparation Uses Storage Safety Supplier Related
ChemicalBook >  Product Catalog >  Flavors and fragrances >  Synthetic fragrances >  Alcohols spices >  Acyclic aliphatic alcohols >  1-UNDECANOL

1-UNDECANOL

Basic information Background Chemical Properties Preparation Uses Storage Safety Supplier Related

1-UNDECANOL Basic information

Product Name:
1-UNDECANOL
Synonyms:
  • 1-Undecanol 0
  • alcooln-undecylique
  • Decyl carbinol
  • decylcarbinol
  • Dlcohol c-11 undecylic
  • Hendecanoic alcohol
  • hendecanoicalcohol
  • Hendecyl alcohol
CAS:
112-42-5
MF:
C11H24O
MW:
172.31
EINECS:
203-970-5
Product Categories:
  • 1-Alkanols
  • Monofunctional & alpha,omega-Bifunctional Alkanes
  • Monofunctional Alkanes
Mol File:
112-42-5.mol
More
Less

1-UNDECANOL Chemical Properties

Melting point:
11 °C (lit.)
Boiling point:
146 °C/30 mmHg (lit.)
Density 
0.83 g/mL at 25 °C (lit.)
vapor pressure 
<1 hPa (20 °C)
FEMA 
3097 | UNDECYL ALCOHOL
refractive index 
n20/D 1.44(lit.)
Flash point:
>230 °F
storage temp. 
Store below +30°C.
solubility 
0.0057g/l insoluble
form 
Liquid
pka
15.20±0.10(Predicted)
color 
Clear colorless to pale yellow
Odor
Faint alcohol.
Odor Type
waxy
Water Solubility 
Not miscible or difficult to mix with water. Soluble in chloroform and ethyl acetate.
JECFA Number
106
BRN 
1698334
Dielectric constant
5.9800000000000004
Dielectric constant
5.9800000000000004
Stability:
Stable. Combustible. Incompatible with strong oxidizing agents, strong acids.
LogP
4.9 at 20℃
CAS DataBase Reference
112-42-5(CAS DataBase Reference)
EPA Substance Registry System
1-Undecanol (112-42-5)
More
Less

Safety Information

Hazard Codes 
Xi,N
Risk Statements 
38-51/53-43
Safety Statements 
37-61-36/37
RIDADR 
UN 3082 9/PG 3
WGK Germany 
2
RTECS 
YQ3155000
TSCA 
Yes
HS Code 
2905 19 00
HazardClass 
9
PackingGroup 
III
Hazardous Substances Data
112-42-5(Hazardous Substances Data)
Toxicity
LD50 orally in Rabbit: 3000 mg/kg

MSDS

More
Less

1-UNDECANOL Usage And Synthesis

Background

1-undecanol, being an organic chemical with molecular formula C11H24O and scented with lemon, is a colorless or pale yellow , water insoluble but alcohol and ether soluble liquid. It is prepared from metal sodium reduction of Ethyl undecanoate, or pressurization and catalytic hydrogenation of ethyl ω- undecanoate , or even obtained by the Grignard reaction of nonyl magnesium bromide and with ethylene oxide. The application of this alcohol is limited. It is only used for some typical aroma oil and fragrance as the fat is solid at low temperature. The citrus rose type and the like only play a secondary and harmonious role and are taken as deodorant. In addition, it is also used to manufacture spices with the scent of acacia, polianthes tuberosa and the like.

Chemical Properties

It is colorless liquid at room temperature; scented with light sweet fat wax mixed with the scent of roses and fruity flavor of citrus, pineapple and the like. But generally the whole body smells scent of rose, as if a little bit of rue flavor. It will smell like orange after highly diluted with the soft sweet flavor of citrus fruit oil. Its concentration is less than 20 × 10-6 with fruity and sweet scent. Unpleasant fat and smell will be produced when the concentration is higher; Melting point :15 ~ 19 ℃; Flash point> 82 ℃; Density: D4250 .828 ~ 0.834; Refractive index: nD200.4370 ~ 1.4430; water insoluble, soluble in most organic solvents, 1: 4.soluble in 60% ethanol

Preparation

It is prepared from undecaethylene reduction. Put 200 ml of anhydrous toluene and 70 g of sodium into a 5-liter three-necked flask, and then heat reflux it until sodium is completely melted. Then stop heating, stir quickly to get the sodium to disperse into sand until the temperature drops to 60 ~ C. Then put 107 grams of ethyl undecanoate into 150ml absolute ethanol solution followed by adding 500ml of absolute ethanol. When the reaction is weakened, heat it in an oil bath until the sodium is completely dissolved. Next remove the ethanol and toluene through the method of steam distillation. Then wash the remaining oily substances with 200ml × 3 hot water. Then wash ether layer with a sequence of water, sodium carbonate and then water after the ethyl ether was extracted. Also dry with magnesium sulfate, boil off the ethyl ether. The product will be finally extracted from the residue after reduced pressure distillation. The yield is 70%.

Uses

Although this undecanol is among the common varieties, but it is still not widely used. It is often used together with undecylenic aldenyde or other fat and aldehydes as the integrator of fragrant volatile of aldehyde. Also it can be well integrated with floral fragrance, citrus cologne, acacia, robinia pseudoacacia, tuberose, violets, clean and grass smell, usually used for rose base. Few application is also available in such pineapple, orange, lemon, lime, orange , cassis, rose food flavors.

Storage

Be sealed and stored in a cool dry place. Also be kept away from fire.

Chemical Properties

Undecyl alcohol has a floral, citrus-like odor and fatty flavor.

Chemical Properties

Colorless liquid; citrus odor. Soluble in 60% alcohol. Combustible.

Occurrence

Reported found in citrus fruits, fresh apple, banana, sour cherry, orange juice, orange peel oil, American cranberry, Vitis vinifera L., parmesan cheese, mushroom, tamarind, coriander seed and leaf, white wine, butter, heated butter, boiled eggs, boiled or uncured pork, plum brandy, coriander leaf, crayfish and oysters.

Uses

1-Undecanol is an antifungal, antioxidant compound. As well, it is used in the synthesis

Uses

1-Undecanol can be used as a precursor in the synthesis of undecanal by chemoselective oxidation using a fluorous derivative of TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl) radical as a catalyst.
It can be also used as a solvent in homogeneous liquid-liquid microextraction method.

Definition

ChEBI: A fatty alcohol that is undecane substituted by a hydroxy group at position 1.

Preparation

By reduction of the corresponding aldehyde.

Synthesis Reference(s)

The Journal of Organic Chemistry, 60, p. 5961, 1995 DOI: 10.1021/jo00123a038

General Description

Undecyl alcohol has been reported as a key volatile constituent of Senecio tenuifolius and Flacourtia montana.

Health Hazard

Recommended Personal Protective Equipment: Goggles and face shield; Symptoms Following Exposure: Liquid can irritate eyes; General Treatment for Exposure: Wash eyes with water for at least 15 min.; Toxicity by Inhalation (Threshold Limit Value): Not pertinent; Short-Term Exposure Limits: Not pertinent; Toxicity by Ingestion: Grade 2, LD50 = 0.5-5 g/kg; Late Toxicity: Data not available; Vapor (Gas) Irritant Characteristics: None; Liquid or Solid Irritant Characteristics: No appreciable hazard. Practically harmless to the skin; Odor Threshold: Not pertinent.

Flammability and Explosibility

Non flammable

Chemical Reactivity

Reactivity with Water No reaction; Reactivity with Common Materials: No reactions; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.

Safety Profile

Moderately toxic by ingestion. A skin irritant. Combustible liquid. Mutation data reported. When heated to decomposition it emits acrid smoke and irritating fumes. See also ALCOHOLS.

Metabolism

See alcohol C-8.

Purification Methods

Purify the alcohol by repeated fractional crystallisation from its melt or by distillation in a vacuum. [Beilstein 1 H 427, 1 IV 1835.]

1-UNDECANOL Preparation Products And Raw materials

Raw materials

1-UNDECANOLSupplier

Dalian Ruiying Technology Co., Ltd. Gold
Tel
0411-86907150 15940963210
Email
609262758@qq.com
Suzhou Guide Fine Material Co.Ltd. Gold
Tel
136-16210669 13914021065
Email
sales@guide-chemicals.com
Yangzhou juhechang Technology Co., Ltd Gold
Tel
0514-0514-83662002 13073488988
Email
13073488988@163.com
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Email
jkinfo@jkchemical.com
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006608290; 18621169109
Email
market03@meryer.com