Carvacrol

Carvacrol is also called isothymol, a natural monoterpene derivative of cymene. It is a colorless to pale yellow liquid with a spicy odor as Thymol. Carvacrol is naturally found in many essential oils especially in thyme oil. It is prepared by the sulfonation reaction of p-Cymene. With a special aroma, Carvacrol is widely used in fragrance formulation, oral product, spice, medicine etc. It’s used as a disinfectant and fungicide due to its capability of killing bacteria and intestinal parasites.

Substance Identification

Synonyms Cymenol | Isothymol | 2-Methyl-5-isopropylphenol
CAS 499-75-2
EINECS 207-889-6
FEMA N/A
HS.CODE 294200
Molecular Formula C10H14O
Molecular Weight 150.22

Toxicological Information

LD50 oral, rat >810mg/kg
LD50 dermal, rabbit 5g/kg

Application & Uses

  • used as antioxidant component
  • used as feed additive ingredients
  • used as food flavoring ingredients
  • used as a disinfectant, astringent ingredients
  • used as insect repellent ingredient
  • used as pharmaceutical intermediate
  • used as natural bacteriostatic ingredients
  • used in the fragrance of daily necessities such as soap

Sales Specification

ITEM VALUE TEST METHOD & UNIT
Odor Character Thyme
Assay 99.5 min @G.C., %
Refractive Index 1.523 @n20D
Specific Gravity 0.972 to 0.980 @d2020

Q&A

How does carvacrol inhibit bacteria and fungi at the molecular and cellular levels, and which performance and regulatory factors matter when evaluating it as a disinfectant or antifungal formulation-active candidate?

Carvacrol primarily acts by entering bacterial or fungal lipid membranes and disturbing membrane organization, increasing ion permeability and disrupting H+ and K+ gradients, proton motive force, and cellular ATP reserves; this mechanism has been experimentally demonstrated in Bacillus cereus (Ultee et al., 1999, Applied and Environmental Microbiology; Ultee et al., 2002, Applied and Environmental Microbiology). In Alternaria alternata, carvacrol can also interfere with chitin- and β-1,3-glucan-related metabolism, weaken cell-wall integrity, and affect glycolysis and stress-related carbohydrate metabolism (Zhao et al., 2024, Postharvest Biology and Technology). It can therefore be evaluated as an active candidate in research formulations for food preservation, feed hygiene, surface mould control, or postharvest protection, but practical efficacy depends on concentration, contact time, pH, substrate, organic load, solubilisation or emulsification system, and the target organism rather than on in-vitro MIC data alone. Its status as a food flavouring or feed flavouring substance does not authorise disinfectant, hygiene biocide, or crop-fungicide claims; in the United States, products claiming to kill or control pathogens will generally fall under FIFRA registration requirements, while EU use requires active-substance approval for the relevant product type and product authorisation (U.S. EPA, 2026, Pesticide Registration Manual; ECHA, 2026, Biocides Supplier or User).

What evidence shows that carvacrol can inhibit neuromuscular function in parasitic nematodes, and what are its known molecular target and application limits?

Available evidence indicates that carvacrol can inhibit neuromuscular activity in selected parasitic nematode models, with muscle nicotinic acetylcholine receptors (nAChRs) as its best-supported functional target; this should not be interpreted as confirmed killing activity against all intestinal parasites. In Parascaris sp. body-muscle flap preparations and Xenopus oocyte expression systems, 300 µM carvacrol completely and irreversibly abolished acetylcholine-induced contractions and antagonised nicotine-sensitive and morantel-sensitive nAChR subtypes (Trailović et al., 2021, Pharmaceuticals). In the pig roundworm Ascaris suum, carvacrol showed predominantly non-competitive nAChR antagonism and enhanced monepantel-mediated inhibition of worm contraction, supporting investigation as an anthelmintic lead but not demonstrating effective or safe combination therapy (Marjanović et al., 2020, Veterinary Parasitology). Carvacrol also inhibited egg hatching, larval development, and adult motility of Haemonchus contortus in vitro, whereas the 65.9% faecal egg-count reduction reported in sheep was obtained with its acetylated derivative, carvacryl acetate, not carvacrol itself (André et al., 2016, Veterinary Parasitology). Carvacrol should therefore not be presented as an established veterinary anthelmintic active ingredient; host safety, effective delivery, residues, interactions with existing anthelmintics, and field resistance risk require systematic evaluation for each target species and indication.

What are the main natural sources of carvacrol, and how should carvacrol content and commercial relevance be compared across plant sources?

Carvacrol is a monoterpenoid phenol found mainly in volatile oils of aromatic Lamiaceae plants, with high-carvacrol chemotypes of Origanum and Thymus as common botanical sources; it also occurs in plants such as Mexican oregano, Lippia graveolens. Carvacrol content should not be assigned as a fixed range from the botanical name alone, because chemotype, origin, harvest stage, plant development, and distillation conditions can substantially change the composition; for example, one Moroccan Origanum compactum oil contained 75.70% carvacrol, whereas Thymus zygis oil from the same study was thymol-dominant and contained only 3.01% carvacrol (Chroho et al., 2024, Antibiotics). Buyers requiring a natural high-carvacrol material should therefore specify species or subspecies, plant part, origin, batch GC result, and a minimum carvacrol specification instead of treating “oregano oil” or “thyme oil” as interchangeable materials. In plants, carvacrol biosynthesis starts from γ-terpinene and proceeds through CYP71D and short-chain dehydrogenase/reductase activity; when the SDR is absent, p-cymene can form, so it is not an obligatory biosynthetic intermediate to carvacrol (Krause et al., 2021, Proceedings of the National Academy of Sciences). For natural positioning, confirm that carvacrol is obtained from a botanical essential oil or a physically separated fraction and obtain process and naturality documentation, because chemically synthesised or chemically modified material does not meet the ISO 9235 concept of a natural aromatic raw material.

What evidence supports carvacrol as a feed additive for production performance, and can it replace antibiotic growth promoters?

Carvacrol and carvacrol-containing phytogenic blends can be evaluated as functional ingredients in antibiotic-free feeding systems, with some broiler studies reporting improvements in growth performance, feed conversion, intestinal morphology, or caecal microbial indicators; however, responses depend on dose, delivery form, basal diet, hygiene challenge, and production conditions (Irawan et al., 2021, Poultry Science). In a 240-broiler study, a phytosome-conjugated carvacrol essential-oil preparation at 100 mg/kg feed improved growth performance, feed efficiency, and intestinal morphology, but the preparation was specified as containing 16.6% carvacrol and should not be interpreted as a 100 mg/kg pure-carvacrol result (Jawale et al., 2024, The Indian Journal of Animal Sciences). Blends containing carvacrol, cinnamaldehyde, and capsicum oleoresin have also shown potential to improve energy utilisation and performance in broilers, but these results apply to the complete blend and cannot be attributed to carvacrol alone (Bravo et al., 2014, Journal of Animal Science). EU authorisations relevant to carvacrol or carvacrol-containing botanical oils place them in the sensory-additive, flavouring-compound category, supporting feed safety and flavouring use under defined conditions rather than authorising a growth-promotion claim (EFSA FEEDAP Panel, 2023, EFSA Journal). Carvacrol may therefore form part of a validated strategy to reduce reliance on AGPs, but current evidence does not support a universal, one-to-one replacement claim across species, farms, and production conditions.

Package

  • Steel Drum, 180kg net each, plastic lining

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GHS Hazard Statements

H-Code H302/H314/H411
P-Code P260/P264/270/273/280
Response P301+P312+P330 P301+P330+P331 P303+P361+P353 P304+P340+P310 P305+P351+P338+P310 P363 P391
Storage P405
Disposal P501
Signal Word Danger
Pictograms GHS05, GHS07, GHS09

Storage

  • air and moisture sensitive
  • containers which are opened must be carefully resealed and kept upright to prevent leakage
  • handle and store under inert gas
  • keep container tightly closed in a dry and well-ventilated place
  • store in cool place

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