ChemicalBook > CAS DataBase List > Citronellol

Citronellol

Product Name
Citronellol
CAS No.
106-22-9
Chemical Name
Citronellol
Synonyms
β-Citronellol;BETA-CITRONELLOL;(S)-Citronellol;CITRONELLOL 96;DL-CITRONELLOL;3,7-DIMETHYL-6-OCTEN-1-OL;FEMA 2309;CITRONELLOL EXTRA;2,6-DIMETHYL-2-OCTEN-8-OL;3,7-DIMETHYL-OCT-6-EN-1-OL
CBNumber
CB0377986
Molecular Formula
C10H20O
Formula Weight
156.27
MOL File
106-22-9.mol
More
Less

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
biological source
synthetic
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)
More
Less

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).
More
Less

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.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
W230915
Product name
Citronellol
Purity
mixture of isomers, natural, ≥95%, FG
Packaging
1 unit
Price
$57.47
Updated
2025/07/31
Sigma-Aldrich
Product number
W230915
Product name
Citronellol
Purity
mixture of isomers, natural, ≥95%, FG
Packaging
1 unit
Price
$57.47
Updated
2025/07/31
Sigma-Aldrich
Product number
W230915
Product name
Citronellol
Purity
mixture of isomers, natural, ≥95%, FG
Packaging
100g
Price
$90.82
Updated
2025/07/31
Sigma-Aldrich
Product number
W230915
Product name
Citronellol
Purity
mixture of isomers, natural, ≥95%, FG
Packaging
1kg
Price
$252
Updated
2025/07/31
Sigma-Aldrich
Product number
W230915
Product name
Citronellol
Purity
mixture of isomers, natural, ≥95%, FG
Packaging
10Kg
Price
$1280
Updated
2025/07/31
More
Less

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

More
Less

Citronellol Suppliers

Alfa Chemistry
Tel
+1-5166625404;
Fax
1-516-927-0118
Email
Info@alfa-chemistry.com
Country
United States
ProdList
20405
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354; +17819995354
Email
marketing@targetmol.com
Country
United States
ProdList
32435
Advantage
58
Aladdin Scientific
Tel
Email
tp@aladdinsci.com
Country
United States
ProdList
57505
Advantage
58
Eastar Chemical Corp
Tel
+86-024-25362369-8022 +8613998281317
Email
angelameng@chinaeastar.com
Country
United States
ProdList
376
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354;
Email
support@targetmol.com
Country
United States
ProdList
39035
Advantage
58
AccuStandard Inc
Tel
--
Fax
--
Email
info@bester.nl
Country
United States
ProdList
5300
Advantage
76
Citrus and Allied Essences Ltd.
Tel
--
Fax
--
Email
galloca@citrusandallied.com
Country
United States
ProdList
90
Advantage
58
International Flavors & Fragrances Inc. (IFF)
Tel
--
Fax
--
Email
info@lucasmeyercosmetics.com
Country
United States
ProdList
55
Advantage
58
Fluorochem Ltd.
Tel
--
Fax
--
Email
enquiries@fluorochem.co.uk
Country
United States
ProdList
4583
Advantage
58
Fleurchem Inc.,
Tel
--
Fax
--
Country
United States
ProdList
119
Advantage
58
Augustus Oils Ltd
Tel
--
Fax
--
Email
essentials@augustus-oils.ltd.uk
Country
United States
ProdList
1404
Advantage
58
Lluch Essence S.L.
Tel
--
Fax
--
Email
web@lluche.com
Country
United States
ProdList
2352
Advantage
58
Alichem Inc.
Tel
--
Fax
--
Email
sales@alichem.com
Country
United States
ProdList
6167
Advantage
58
Redox Scientific
Tel
--
Fax
--
Email
info@redoxsci.com
Country
United States
ProdList
2380
Advantage
58
Selleck Chemicals LLC
Tel
--
Fax
--
Email
sales@selleckchem.com
Country
United States
ProdList
1848
Advantage
58
Advanced Biotech - ABT
Tel
--
Fax
--
Country
United States
ProdList
260
Advantage
58
Prodasynth
Tel
--
Fax
--
Email
info@prodasynth.com
Country
United States
ProdList
423
Advantage
58
Frutarom (F&F Ingredients)
Tel
--
Fax
--
Email
info@frutarom.com
Country
United States
ProdList
280
Advantage
58
Elan Chemical Inc.
Tel
--
Fax
--
Email
sales@elan-chemical.com
Country
United States
ProdList
114
Advantage
65
First Continental International (FCI)
Tel
--
Fax
--
Email
sales@fci-nj.com
Country
United States
ProdList
178
Advantage
58
PRIVI Organics Ltd.
Tel
--
Fax
--
Email
sales@privi.co.in
Country
United States
ProdList
43
Advantage
62
Vigon International, Inc.
Tel
--
Fax
--
Email
jpassamonte@vigoninternational.com
Country
United States
ProdList
1268
Advantage
64
MedChemExpress
Tel
--
Fax
--
Email
sales@medchemexpress.com
Country
United States
ProdList
6398
Advantage
58
Riedel-de Haen AG
Tel
--
Fax
--
Country
United States
ProdList
6773
Advantage
87
TCI America
Tel
--
Fax
--
Email
sales@tciamerica.com
Country
United States
ProdList
6909
Advantage
75
Frontier Scientific, Inc.
Tel
--
Fax
--
Email
sales@frontiersci.com
Country
United States
ProdList
6222
Advantage
86
Interchim Inc.
Tel
--
Fax
--
Email
web@interchiminc.com
Country
United States
ProdList
301
Advantage
50
Spectrum Chemical Mfg. Corp.
Tel
--
Fax
--
Email
marketing@spectrumchemical.com
Country
United States
ProdList
3113
Advantage
60
Waterstone Technology, LLC
Tel
--
Fax
--
Email
sales@waterstonetech.com
Country
United States
ProdList
6786
Advantage
30
Penta Manufacturing Company
Tel
--
Fax
--
Email
sales@pentamfg.com
Country
United States
ProdList
5076
Advantage
65
Advanced Synthesis Technologies
Tel
--
Fax
--
Email
sales@advancedsynthesis.com
Country
United States
ProdList
4775
Advantage
61
Chiral Management
Tel
--
Fax
--
Email
sales@chiralmanagement.com
Country
United States
ProdList
1332
Advantage
30
SRS Aromatics Ltd
Tel
--
Fax
--
Email
info@srsaromatics.co.uk
Country
United States
ProdList
2315
Advantage
46
INDOFINE Chemical Company, Inc.
Tel
--
Fax
--
Email
chemical@indofinechemical.com
Country
United States
ProdList
6176
Advantage
69
City Chemical LLC
Tel
--
Fax
--
Email
sales@citychemical.com
Country
United States
ProdList
6708
Advantage
72
3B Scientific Corporation
Tel
--
Fax
--
Email
sales@3bsc.com
Country
United States
ProdList
6718
Advantage
47
HONEST JOY HOLDINGS LIMITED
Tel
--
Fax
--
Email
sales@honestjoy.cn
Country
United States
ProdList
6675
Advantage
54
AK Scientific, Inc.
Tel
--
Fax
--
Email
sales@aksci.com
Country
United States
ProdList
6347
Advantage
65
Varian, Inc.
Tel
--
Fax
--
Email
custserv@varianinc.com
Country
United States
ProdList
224
Advantage
85
Sciencelab.com, Inc.
Tel
--
Fax
--
Email
accounting@sciencelab.com
Country
United States
ProdList
4159
Advantage
82
Advance Scientific & Chemical
Tel
--
Fax
--
Email
sales@advance-scientific.com
Country
United States
ProdList
6419
Advantage
71
Moore Ingredients, Ltd.
Tel
--
Fax
--
Email
sdagnillo@amtodd.com
Country
United States
ProdList
126
Advantage
64
Fine Chem Trading LTD
Tel
--
Fax
--
Email
chemfinder@chemfinder.co.uk
Country
United States
ProdList
1609
Advantage
64
Pfaltz & Bauer, Inc.
Tel
--
Fax
--
Email
sales@pfaltzandbauer.com
Country
United States
ProdList
6828
Advantage
72
Eastern Chemical Corp.
Tel
--
Fax
--
Email
eastern@u-g.com
Country
United States
ProdList
2786
Advantage
34
BASF Corporation
Tel
--
Fax
--
Country
United States
ProdList
573
Advantage
86
Spectrum Chemicals & Laboratory Products
Tel
--
Fax
--
Email
sales@spectrumchemical.com
Country
United States
ProdList
6699
Advantage
77
Bedoukian Research, Inc.
Tel
--
Fax
--
Email
customerservice@bedoukian.com
Country
United States
ProdList
737
Advantage
68
Fisher Scientific
Tel
--
Fax
--
Email
sales@fishersci.com
Country
United States
ProdList
2337
Advantage
86
Lyondell Chemical Company
Tel
--
Fax
--
Country
United States
ProdList
79
Advantage
81
More
Less

View Lastest Price from Citronellol manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
Citronellol 106-22-9
Price
US $0.00/kg
Min. Order
1000kg
Purity
98.0%
Supply Ability
100ton/month
Release date
2023-01-14
Hebei Chuanghai Biotechnology Co., Ltd
Product
Citronellol 106-22-9
Price
US $1.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
10 mt
Release date
2024-11-06
HebeiShuoshengImportandExportco.,Ltd
Product
Citronellol 106-22-9
Price
US $6.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
2000KG/Month
Release date
2024-08-02

106-22-9, CitronellolRelated Search:


  • 2,6-DIMETHYL-2-OCTEN-8-OL
  • (+/-)-CITRONELLOL
  • CITRONELLOL
  • CITRONELLOL PRIME
  • CITRONELLOL EXTRA
  • CITRONELLOL 80
  • CITRONELLOL 90/92
  • CITRONELLOL 96
  • CITRONELLOL 96/98
  • CITRONELLOL AJ
  • CITRONELLOL, DL-B-
  • DL-B-CITRONELLOL
  • DL-CITRONELLOL
  • FEMA 2309
  • 6-OCTEN-1-OL, 3,7-DIMETHYL
  • 3,7-DIMETHYL-6-OCTEN-1-OL
  • 3,7-DIMETHYL-OCT-6-EN-1-OL
  • (26489-01-0) citronellol
  • 2,6-Dimethyl-2-coten-8-ol
  • 3,7-dimethyl-6-octanol
  • 3,7-dimethyl-6-octen-1-o
  • 3,7-dimethyl-6-octen-1-ol (citronellol)
  • 3,7-Dimethyl-6-octen-l-ol
  • Cephrol
  • Elenol
  • Rodinol
  • CITRONELLOL 96 FCC
  • CITRONELLOL AJ FCC
  • (S)-Citronellol
  • citronellol,3,7-dimethyl-6-octen-1-ol,β-citronellol,(+)-citronellol,rodinol,DL-citronellol
  • 1-CITRONELLOL
  • CITRONELLOL, NATUERLICH
  • 2,3-Dihydrogeraniol
  • (+/-)-B-CITRONELLOL WITH GC
  • CITRONELLOL BRI FCC
  • FEMA 2307
  • (+/-)-BETA-CITRONELLOL
  • BETA-CITRONELLOL
  • CitroneIlol
  • 5-Vinylpicoline
  • [R,(+)]-3,7-Dimethyl-7-octen-1-ol
  • [R,(+)]-3,7-Dimethyl-7-octene-1-ol
  • 2,6-Dimethyl-2-octene-8-ol
  • NSC-8779
  • CITRONELLOL FOR SYNTHESIS 5 ML
  • CITRONELLOL FOR SYNTHESIS 250 ML
  • β-Citronellol,(±)-β-Citronellol, 3,7-Dimethyl-6-octen-1-ol
  • Citronellol, 95% 100ML
  • Citronellol, 95% 500ML
  • beta-Citronellol 95%
  • (±)-b-Citronel
  • β-Citronello
  • Citronellol beta-Citronellol
  • CITRONELLOL FCC
  • CITRONELLOL, NATURAL
  • (±)-β-Citronellol, 3,7-Dimethyl-6-octen-1-ol
  • CITRONELLOL SOLUTION
  • Dihydrog eranio