Citronellol Property

Melting point:

77-83 °C(lit.)

Boiling point:

225 °C(lit.)

alpha 

-0.3～+0.3°(D/20℃)(neat)

Density 

0.857 g/mL at 25 °C(lit.)

vapor density 

5.4 (vs air)

vapor pressure 

~0.02 mm Hg ( 25 °C)

refractive index 

n20/D 1.456(lit.)

FEMA 

2309 | DL-CITRONELLOL

Flash point:

209 °F

storage temp. 

2-8°C

solubility 

Chloroform, Methanol (Sparingly)

pka

15.13±0.10(Predicted)

form 

Liquid

color 

Clear almost colorless

Odor

at 100.00 %. floral leather waxy rose bud citrus

Odor Type

floral

Water Solubility 

SLIGHTLY SOLUBLE

Merck 

14,2330

JECFA Number

1219

BRN 

1721507

Stability:

Stable. Incompatible with oxidizing agents.

InChIKey

QMVPMAAFGQKVCJ-UHFFFAOYSA-N

LogP

3.41 at 25℃

CAS DataBase Reference

106-22-9(CAS DataBase Reference)

NIST Chemistry Reference

6-Octen-1-ol, 3,7-dimethyl-(106-22-9)

EPA Substance Registry System

Citronellol (106-22-9)

Safety

Hazard Codes 

Xi,N

Risk Statements 

36/37/38-51/53-43-36/38

Safety Statements 

26-36-24/25-61-37-24

WGK Germany 

1

RTECS 

RH3400000

Hazard Note 

Irritant

TSCA 

Yes

HS Code 

29052220

Hazardous Substances Data

106-22-9(Hazardous Substances Data)

Toxicity

The acute oral LD₅₀ value in rats was reported as 3.45 g/kg (3.21-3.69 g/kg) (Moreno, 1973). The acute dermal LE>50 value in rabbits was reported as 2.65 g/kg (1.78-3.52 g/kg) (Moreno, 1973). The im LD₅₀ value in mice was reported as 4 g/kg (Northover & Verghese, 1962).

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H317May cause an allergic skin reaction

H319Causes serious eye irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P272Contaminated work clothing should not be allowed out of the workplace.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

Citronellol Chemical Properties,Usage,Production

Description

Citronellol is a kind of natural occurring acyclic monoterpenoid which can be found in citronella oils such as Cymbopogon nardus ((+)-citronellol) and rose oils and Pelargonium geraniums ((-)-citronellol). In addition to be extracted from natural oils, it can also be manufactured by the hydrogenation of geraniol or nerol. It is mainly used in perfumes and insects repellents as well as being used as a mite attractant. It should be noted that it is an excellent mosquito repellent at short distances. Combination with beta-cyclodextrin can make it has an average duration time of 1.5 hour against the mosquitoes. It can also be used for the manufacture of rose oxide. One of its most common applications is for adding floral and citrus notes to perfumes, soaps and cosmetics.

Chemical Properties

colourless liquid with a characteristic, rose-like, smell

Chemical Properties

Citronellol has a characteristic rose-like odor. Because odor plays such an important part in selecting this material, there may be special grades of citronellol that do not meet the Essential Oil Association specification. These limits have been broadened enough to include best qualities of commercial citronellol and chemically pure citronellol. l-Citronellol has a sweet, peach-like flavor; d-citronellol has a bitter taste.

Occurrence

l-Citronellol has been found in the plants of the Rosaceae family; d- and dl-citronellol have been identified in Verbenaceae, Labiatae, Rutaceae, Geraniaceae and others; citronellol has been reported in about 70 essential oils and in the oil of Rosa bourbonia; the Bulgarian rose oil has been reported to contain more than 50% l-citronellol, whereas East African geranium contains more than 80% of the d-isomer; the natural product is always optically active. Reported found in guava fruit, orange, bilberry, blackcurrant, nutmeg, ginger, corn mint oil (Mentha arvensis L. var. piperascens), mustard, pennyroyal oil (Mentha pulegium L.), hop oil, tea, coriander seed, cardamom, beer, rum, and apple juice.

Uses

rac-Citronellol is a monoterpene found in the essential oil of various plants with antihypertensive properties. It possesses hypotensive actions due to its vasodilator abilities and is a phytochemical used in perfumes and insect repellents.

Uses

Perfumery, flavoring agent.

Uses

citronellol is a constituent of plant essential oils. Found abundantly in eucalyptus oil. It is used for masking odor or providing a fragrance component to a cosmetic product.

Definition

ChEBI: A monoterpenoid that is oct-6-ene substituted by a hydroxy group at position 1 and methyl groups at positions 3 and 7.

Preparation

By reduction of citronellal or geraniol or by fractional distillation of such essential oils as geranium and citronella (Bedoukian, 1967).

Aroma threshold values

Detection at 11 ppb to 2.2 ppm; l-form, 40 ppb

Taste threshold values

Taste characteristics at 20 ppm: floral, rose, sweet and green with fruity citrus nuances.

Synthesis Reference(s)

The Journal of Organic Chemistry, 60, p. 2260, 1995 DOI: 10.1021/jo00112a056
Synthesis, p. 391, 1976
Tetrahedron Letters, 30, p. 5677, 1989 DOI: 10.1016/S0040-4039(00)76168-5

General Description

Citronellol is a volatile monoterpenic primary alcohol mainly found in the essential oil of plants such as Pelargonium graveolens, Cymbopogon winterianus and Rosa damascena. It is also one of the glycosidically bound aroma compounds in ginger.

Flammability and Explosibility

Non flammable

Safety Profile

Poison by intravenous route. Moderately toxic by ingestion, skin contact, and intramuscular routes. A severe skin irritant. A combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes. See also ALCOHOLS.

Synthesis

It is generally accepted to distinguish rhodinol as the product isolated from geranium consisting of a mixture of l-citronellol and geraniol, whereas the name l-citronellol should be used to indicate the corresponding synthetic product with the highest level of purity; dl-citronellol can be prepared by catalytic hydrogenation of geraniol or by oxidation of allo-cyrnene; l-citronellol is prepared from (+) d-pinene via (+) cis-pinene to (+) 2,6-dimethyl-2,7-octadiene and, finally, isolating l-citronellol by hydrolysis of the aluminum-organo compound.

Purification Methods

Purify them bydistillation through a cannon packed (Ni) column and the main cut collected at 84o/14mm and redistilled. Also purify via the benzoate. [IR: Eschenazi J Org Chem 26 3072 1961, Naves Bull Soc Chim Fr 505 1951, Beilstein 1 IV 2188.]

References

https://eic.rsc.org/magnificent-molecules/citronellol/2000020.article
https://en.wikipedia.org/wiki/Citronellol