Citronella Oil

Citronella oil, member of a class of naturally occurring organic substances called terpenes, which is obtained from the leaves of the oil grasses Cymbopogon nardus and C.winterianus. As the wide range of uses, Citronella oil is mindly used for medicines to perfumes for soaps. Two derivatives of citronella oil include the alcohol citronellol and the aldehyde citronellal.

Substance Identification

Synonyms
CAS 8000-29-1
EINECS 616-771-7
FEMA 2308
HS.CODE 330129
Molecular Formula N/A
Molecular Weight N/A

Application & Uses

  • used for medicines
  • used as perfumes for soaps

Sales Specification

ITEM VALUE
Appearance Colorless to pale yellow clear liquid
Refractive Index, @ n20/D 1.466 to 1.473
Relative Density, @ d20/20 0.880 to 0.900
Optical Rotation, @20°C, ° -5 to 0

Q&A

Why does citronellal content in citronella oil determine its value as feedstock for synthetic menthol production?

In menthol syntheses that proceed via the citronellal route, citronellal itself is the pivotal intermediate: under Lewis‑acid catalysis (for example ZnBr₂ or related systems) it cyclises to isopulegol, which is then hydrogenated to (−)-menthol, so the citronellal assay in citronella oil effectively maps onto the potential menthol yield from that feedstock (Dylong, 2022; Plößer et al., 2014). Java‑type citronella oil typically contains about 32–45% citronellal, whereas Ceylon‑type contains only around 5–16%, making the Java type far more economical for menthol manufacturers on a per‑tonne basis. Industrial processes developed by Takasago and BASF both route through optically enriched (+)-(R)-citronellal, usually generated from myrcene or citral via asymmetric catalysis, but for producers who use essential‑oil fractionation to obtain citronellal, the assay percentage remains the primary value driver, with optical rotation serving as a secondary check on whether the citronellal stream approximates the desired enantiomeric composition. Total alcohol content in citronella oil is of limited importance for menthol synthesis itself, yet becomes commercially relevant if the buyer also plans to recover citronellol as a co‑product, so procurement teams should prioritise citronellal content first, then weigh optical rotation and total alcohols according to whether co‑product strategies are part of their business model

Which compositional differences between Java‑type and Ceylon‑type citronella oil affect downstream citronellol recovery for perfumery applications?

Java‑type citronella oil from Cymbopogon winterianus is characterised by a higher citronellal content (about 32–45%) together with moderate‑to‑high geraniol (roughly 11–24%) and citronellol in the 11–15% range, whereas Ceylon‑type oil from C. nardus contains only about 5–15% citronellal and typically 6–8% citronellol but a relatively higher alcohol‑to‑aldehyde ratio and more methyl isoeugenol and related aromatics. For purely yield‑driven citronellol fractionation, Java‑type oil generally offers better economics in terms of recoverable citronellol tonnage per tonne of oil, given its higher absolute citronellol and total alcohol content (often 80–90% vs 55–65% for Ceylon), but perfumery teams aiming for a softer, rose‑type citronellol note and specific alcohol/aldehyde balance—and needing to manage methyl isoeugenol under regulatory limits—may prefer Ceylon‑type despite its lower citronellal. The specification set you cite (refractive index 1.466–1.473, relative density 0.880–0.900, and an optical‑rotation range around −5 to 0°) matches typical Java‑type profiles; buyers seeking Ceylon‑type should expect slightly higher density (about 0.894–0.910) and refractive index (around 1.479–1.487) and should always confirm the botanical origin and GC‑MS composition on the supplier's COA to ensure they are truly sourcing C. nardus rather than C. winterianus.

Can refractive index and optical rotation data predict the citronellol yield recoverable from citronella oil?

Refractive index and optical rotation offer indirect indicators of citronella oil composition, but they do not reliably predict the actual citronellol yield recoverable from a batch. For Java‑type oils, refractive index is typically specified around 1.466–1.474, while Ceylon‑type sits higher, around 1.479–1.485, reflecting broader differences in alcohol‑to‑aldehyde balance between chemotypes; within a single chemotype, small shifts toward the upper end of a narrow RI band often correlate with a richer total terpene‑alcohol fraction, but this correlation is driven by citronellal, citronellol, geraniol and esters together and cannot be translated directly into citronellol percentage. Optical rotation (for example, ranges like −5 to 0°) mainly captures the overall enantiomeric balance of multiple chiral constituents rather than the absolute concentration of citronellol or citronellal, making it more suitable for chemotype identification and batch‑to‑batch consistency checks than for yield prediction. In procurement, the robust approach is to request a GC composition profile with explicit assays for citronellal, citronellol and geraniol; refractive index and optical rotation should be treated as supporting quality and identity parameters, not as substitutes for full compositional analysis when evaluating new suppliers or estimating citronellol recovery economics.

Package

  • Galvanized Iron Drum, 180kg net each
  • Galvanized Iron Drum, 200kg net each

Preview all the spec of packaging

GHS Hazard Statements

H-Code H315/H317/H318/H334/H335
P-Code P261/P264/P271/P272/P273/P280
Response P302+P352 P304+P340 P305+P351+P338 P310 P333+P313 P342+P311 P362+P364
Storage P403+P233 P403+P235 P405
Disposal P501
Signal Danger
UN Number UN 1760 8/PG 2

Storage

  • flammable materials should be stored in a separate safety storage cabinet or room
  • ground all equipment containing material
  • keep away from heat
  • keep away from sources of ignition
  • keep container dry
  • keep container tightly closed. keep in a cool, well-ventilated place
  • keep in a cool place

Relation Products

Remark

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The above information is believed to be accurate and represents the best explanation currently available to us. However, no liability is assumed for any consequences arising from the use of this content. The technical standards for our products are developed and updated jointly by our customers and ourselves; where any changes occur, the latest specification shall prevail and will be confirmed in the relevant contract.All suggestions and data provided are based on information we consider to be reliable and are offered in good faith, but without any guarantee, as the conditions and methods of use of our products are beyond our control. Foreverest® makes no warranties, whether express or implied, regarding the accuracy, completeness or suitability of this information, and expressly disclaims any implied warranty of fitness for a particular purpose. Prospective users should conduct their own tests and evaluations to determine the suitability of Foreverest® materials and any recommendations for their intended applications before adoption, and, where appropriate, should obtain confirmation or approval from the relevant regulatory authorities.Any references in this page to patents or patented technologies, including descriptive material derived from patents or citations of specific patent numbers, are provided for information only. They must not be interpreted as a recommendation to use our products in a manner that could infringe any third‑party patent, nor as a grant of any licence or permission to use patents owned by Foreverest®.

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