ChemicalBook > Product Catalog >Flavors and fragrances >Synthetic fragrances >Aldehydes spices >Terpene aldehyde >Citronellal

Citronellal

Citronellal Structure
CAS No.
106-23-0
Chemical Name:
Citronellal
Synonyms
Citronella;RHODINAL;3,7-dimethyl-6-octena;3,7-dimethyloct-6-enal;3,7-DIMETHYL-6-OCTENAL;Citronellel;CITRONELLAL NATURAL;CitroneL;FEMA 2307;d-rhodinal
CBNumber:
CB3715673
Molecular Formula:
C10H18O
Molecular Weight:
154.25
MOL File:
106-23-0.mol
MSDS File:
SDS
Modify Date:
2024/7/26 15:15:06

Citronellal Properties

Melting point -16°C (estimate)
alpha D25 +11.50°
Boiling point 207 °C(lit.)
Density 0.857 g/mL at 25 °C(lit.)
vapor pressure 14 hPa (88 °C)
refractive index n20/D 1.451(lit.)
FEMA 2307 | CITRONELLAL
Flash point 169 °F
storage temp. Store below +30°C.
solubility Chloroform (Soluble), Methanol (Sparingly)
form Liquid
color Clear light yellow
Specific Gravity 0.858 (20/4℃)
PH 7 (H2O)
Odor at 10.00 % in dipropylene glycol. sweet dry floral herbal waxy aldehydic citrus
Odor Type floral
explosive limit 1.2-4.5%(V)
Water Solubility Slightly miscible with water and ethanol.
Sensitive Air Sensitive
Merck 14,2329
JECFA Number 1220
BRN 1720789
Stability Hygroscopic
InChIKey NEHNMFOYXAPHSD-UHFFFAOYSA-N
LogP 3.62 at 25℃
CAS DataBase Reference 106-23-0(CAS DataBase Reference)
NIST Chemistry Reference 6-Octenal, 3,7-dimethyl-(106-23-0)
EPA Substance Registry System Citronellal (106-23-0)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H317-H319
Precautionary statements  P261-P264-P272-P280-P302+P352-P305+P351+P338
Hazard Codes  Xn,Xi,N
Risk Statements  38-43-51/53-36/37/38-22
Safety Statements  36/37-61-37/39-26-36
RIDADR  UN 3082 9/PG 3
WGK Germany  3
RTECS  RH2140000
8
Autoignition Temperature 202 °C
TSCA  Yes
HS Code  29121900
Toxicity LD50 orally in Rabbit: 2420 mg/kg LD50 dermal Rabbit > 2500 mg/kg
NFPA 704
2
0 0

Citronellal price More Price(11)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) W230715 (±)-Citronellal natural, ≥85%, FCC, FG 106-23-0 1SAMPLE-K ₹5196 2022-06-14 Buy
Sigma-Aldrich(India) W230715 (±)-Citronellal natural, ≥85%, FCC, FG 106-23-0 1KG ₹15328.2 2022-06-14 Buy
Sigma-Aldrich(India) W230715 (±)-Citronellal natural, ≥85%, FCC, FG 106-23-0 4KG ₹45638.2 2022-06-14 Buy
Sigma-Aldrich(India) W230707 (±)-Citronellal ≥85%, FG 106-23-0 1SAMPLE-K ₹5141.88 2022-06-14 Buy
Sigma-Aldrich(India) W230707 (±)-Citronellal ≥85%, FG 106-23-0 1KG ₹15414.8 2022-06-14 Buy
Product number Packaging Price Buy
W230715 1SAMPLE-K ₹5196 Buy
W230715 1KG ₹15328.2 Buy
W230715 4KG ₹45638.2 Buy
W230707 1SAMPLE-K ₹5141.88 Buy
W230707 1KG ₹15414.8 Buy

Citronellal Chemical Properties,Uses,Production

Chemical Properties

(?)-Citronellal occurs in Java citronella oil at a concentration of 35%. Racemic citronellal is the main constituent of E. citriodora oil with a content of up to 85%.
Pure citronellal is a colorless liquid with a refreshing odor, reminiscent of lemon balm. Upon catalytic hydrogenation, citronellal yields dihydrocitronellal, citronellol, or dihydrocitronellol, depending on the reaction conditions. Protection of the aldehyde group, followed by addition of water to the double bond in the presence of mineral acids or ion-exchange resins results in the formation of 3,7-dimethyl-7-hydroxy-octan-l-al (hydroxydihydrocitronellal). Acid-catalyzed cyclization to isopulegol is an important step in the synthesis of (?)-menthol.

Occurrence

The d-form of citronellal has been reported in the oil of citronella (Ceylon, Jammus, Kaschmis), in the oil from leaves of Barosma pulchella, in the oil from roots of Phebalium nudum and in the oils of Eucalyptus citriodora, Leptospermum citratum and Baeckea citriodora. The /-form is present in the oils of Backhousia citriodora var. A, E. citriodora, Litsea cubeba (fruits) and lemongrass. Citronellal is generally present also in the oils of lemon, mandarin, Lavandula delphinensis, Ocimum canum f. citrata and many others (Fenarolis Handbook of Flavor Ingredients, 1971).

Uses

rac-Citronellal is a monoterpenoid and the major isolate in citronella oil. Citronella oil is an essential oil bearing insecticidal properties. rac-Citronellal is also often used as a fragrance ingred ient.

Preparation

Citronellal is still isolated from essential oils in considerable quantities; it is also produced synthetically.
1) Isolation from essential oils:(+)-Citronellal is obtained from citronella oils by fractional distillation. Racemic citronellal is isolated from E. citriodora oil; when necessary, it is purified by using an addition compound, for example, the bisulfite derivative.
2) Synthesis from geraniol or nerol: Racemic citronellal can be obtained by vaporphase rearrangement of geraniol or nerol in the presence of, for example, a barium-containing copper–chromium oxide catalyst.
3) Synthesis from citronellol: Racemic citronellal can also be obtained by dehydrogenation of citronellol under reduced pressure with a copper chromite catalyst.
4) Synthesis from citral: Selective hydrogenation of citral to citronellal can be accomplished in the presence of a palladium catalyst in an alkaline alcoholic reaction medium. A continuously operating process for the hydrogenation on a palladium catalyst in the presence of trimethylamine has been developed.
5) Synthesis from myrcene: (+)- and (?)-Citronellal are available from myrcene via geranyldiethylamine, which is enantioselectively isomerized to (+)- or (?)-citronellalenamine. Hydrolysis yields pure (+)- or (?)-citronellal; see monograph menthol.

Definition

ChEBI: A monoterpenoid, the main component of citronella oil which gives it its distinctive lemon aroma.

Essential oil composition

Citronella oil contains a number of fragrant fractions of which citronellal, geraniol and citronellol are the major components. Ceylon citronella oil contains 55 to 65% total acetylizable alcohols (calculated as citronellol) and 7 to 15% total aldehyde (calculated as citronellal). The main constituents are geraniol (18 to 20%), citronellol (6.4 to 8.4%), citronellal (5 to 15%), geranyl acetate (2%); limonene (9 to 11%) and methyl isoeugenol (7.2 to 11.3%). Other constituents are camphene, caryophyllene, linalool, citral (neral and geranial), methylheapenone, methyleugenol, l-borneol, nerol, eugenol and farnesol.* Java citronella oil contains not less than 35% alcohols (calculated as citronellol) and not less than 35% aldehydes (calculated as citronellal). The Java type appears to have higher concentrations of citronellol (35%) and geraniol (21%) than does the Ceylon type (citronellol 10% and geraniol 18%).

General Description

(±)-Citronellal was studied for its fumigant antifungal activity against Pyricularia (Magnaporthe) grisea.

Metabolism

Feeding 50 g citronellal to rabbits was followed by the isolation of 13 g of a crystalline glucuronide, which proved to be p-menthane-3.8-diol-D-glucuronide. The citronellal appeared to have been cyclized and the glucuronide obtained was identical with that obtained on feeding p-menthane-3,8-diol (menthoglycol) (Kühn & Low, 1938). However, evidence was produced to show that the cyclization was not, strictly speaking, a biological reaction, but a chemical one which took place in the stomach under the influence of the gastric hydrochloric acid. The conjugation of the menthoglycol with glucuronic acid was, of course, a purely biological reaction. It was found that on shaking 20 g citronellal with 200 ml 0-5% HCl for 48 hr at 37 C, 12 g menthoglycol was formed (Kühn & Low, 1938).

Global( 445)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Jayshree Aromatics Pvt.Ltd. +91-9925031256 +91-9925031256 Gujarat, India 89 58 Inquiry
HJ AROCHEM +91-8690768060 +91-9724420086 Ahmedabad, India 171 58 Inquiry
Salasar Aromatics +91-9810053845 +91-9811438451 Uttar Pradesh, India 14 58 Inquiry
Privi Speciality Chemicals Ltd. +91-2233043500 +91-2233043500 Mumbai, India 63 58 Inquiry
Neeru Menthol Pvt Ltd +91-8884114465 +91-9837322285 New Delhi, India 70 58 Inquiry
Neelam Aqua & Speciality Chem. (P) Ltd. +91-9829069545 +91-9829060543 Rajasthan, India 38 58 Inquiry
Gyan Flavours Export Pvt. Ltd. 91-11-22814681 Delhi, India 19 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
Central Drug House(P) Ltd. 91-11-49404040 New Delhi, India 6160 58 Inquiry
2,3-Dihydrocitral d-rhodinal Levo-citronellal 3,7-DIMETHYL-6-OCTEN-1-AL (+/-)-3,7-DIMETHYL-6-OCTENAL (+/-)-CITRONELLAL CITRONELLAL CITRONELLAL 80 FEMA 2307 CITRONELLAL NATURAL 85+% FCC (+/-)-CITRONELLAL, 80-90% Citronellal, pract., 93% citronellal,3,7-dimethyl-6-octenal,rhodinal CITRONELLAL FCC, NATURAL CITRONELLAL SYNTHETIC CITRONELLAL, (-)-(SG) Citronellal,85+%,tech. Citronellal,93%,pract. CITRONELLAL FOR SYNTHESIS 100 ML rac-Citronellal (+/-)-Citronellal >=95.0% (GC) Citronellal 3,7-Dimethyl-6-octenal 6-ocetnal,3,7-dimethyl- 6-octenal,3,7-dimethyl- 6-Octenal,3,7-dimethyl-,(±)- b-citronellal dl-Citronellal CITRONELLAL FOR SYNTHESIS 500 ML Citronellal for synthesis CitroneL Rhodinal (Citronellal) Methoprene Impurity 6 Citronellal USP/EP/BP RHODINAL 3,7-dimethyl-6-octena 3,7-dimethyloct-6-enal 3,7-DIMETHYL-6-OCTENAL CITRONELLAL NATURAL Citronella Citronellel 3,7-dimethyloct-6-en-1-al GLY-HIS-LYS ACETATE SALT 72957-37-0 Citronellal and Citronellal 106-23-0 5949-05-03 5949-5-3 C9H17CHO CH32CCHCH2CH2CHCH3CH2CHO Organic Building Blocks Building Blocks Analytical Standards Alphabetic Analytical Chromatography Product Catalog Carbonyl Compounds C10 to C21 CI - CL Aldehydes Furans ,Coumarins