Rosemary Therapeutic Grade Essential Oils (Rosemarinus officianlis)

Rosemary Therapeutic Grade Essential Oils
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Botanical name   Rosmarinus officinalis

Family   Lamiaceae

Source   Herb

Origin  Morocco

Processing Method  Steam Distillation

Color/Consistency  A thin, clear, colourless to pale yellow liquid.

Aroma  A top note with a strong aroma, Rosemary has a fresh, strong, woody and herbal scent.

Blends With  Basil, Bergamot, Black Pepper, Cedar Atlas, Cinnamon, Eucalyptus-Lemon, Clary Sage, Elemi, Eucalyptus-Radiata, Frankincense, Geranium, Grapefruit, Cistus / Labdanum, Lavender, Lemon, May Chang, Mandarin, Sweet Marjoram, Niaouli, Myrrh, Oregano, Peppermint, Petitgrain, Pine, Ravensara aromatica, Tea Tree, and Thyme.

Product Abstract

Rosemary oil is very good for the skin because of its astringent properties.  This essential oil is rich in nutrients and has been used as a favorite ingredient to many skin care products.  Below are some of the benefits Rosemary oil can do to your skin.  The plant is very rich in polyphenols and flavonoids. These have with high antioxidant properties and are used for problems involving the central nervous system, cardio vascular system, liver treatments, and respiratory systems among many others. Rosemary leaves have been traditionally used to treat a variety of conditions including dyspepsia, headache and nervous tension.


Rosemary history contains an interesting bit of folklore from the 14th Century. Rosemary root was “seethed in wine vinegar” and the lotion was then used to wash the feet of a thief. The lotion was thought to sap the strength of the robber so that he would not longer commit robbery, steal or do any further harm. In a humorous aside, our original source for this bit of folklore questions their own source with, “How the potential or suspected thief is to be persuaded to wash his feet, the manuscript does not divulge.

Harvesting/Extraction Information

Rosemary oil is obtained by steam distillation of the fresh leaves and flowering tops of the plant. It is a colorless to pale yellow liquid having the characteristic odor of the herb and camphoraceous taste. The volatile oil consists of borneol, camphene, bornyl acetate, cineol, pinene and camphor.

Common Usage

  • Relief From Anxiety
  • Improves Memory And Learning
  • Stop Headaches
  • Relieves Joint Pain And Muscle Aches
  • Instant Relief From Coughs and Colds
  • Stop Dandruff In Its Tracks
  • Reduce The Appearance Of Stretch Marks
  • The Perfect Insecticide
  • All-Purpose Cleaning Spray
  • Stop Wrinkles With This Recipe
  • Superior Stress Relief
  • Supports The Immune System


Rosemary oil may, at times, cause allergic reactions, so it should only be used if prescribed or after thorough consultation with your medical specialist. Since rosemary oil is volatile in nature, the oil occasionally causes vomiting and spasms. Therefore, it should never be ingested. It is strongly suggested that rosemary essential oil should not be used by pregnant, breastfeeding or nursing women. Excessive use of the oil may even lead to miscarriage or a disability in the fetus.

Key constituents

1,8-Cineole 20.0%

Borneol 15.6%

Camphor 15.3%

Verbenone 8.4%

a-Pinene 8.3%

Bornyl acetate 4.9%

Linalool 3.5%

Camphene 3.1%

b-Caryophyllene 2.2%

a-Terpineol 2.0%

p-Cymene 1.8%

ar-Curcumene 1.3%

1-Nonanol 1.2%

Terpinen-4-ol 1.0%

Quality  Rosemary oil may be adulterated with eucalyptus oil, white camphor oil, turpentine oil and  fractions thereof

Safety summary
Hazards  May be neurotoxic, based on camphor content
Contraindications  Do not apply to or near the face of infants or children.
Maximum use levels Camphor CT 16.5% ; 513 mg

Our safety advice
The maximum doses recommended above for the camphor and a-pinene CT oils are based on camphor contents of 27.3% and 20.7%, respectively, and dermal and oral limits of 4.5% and 2 mg/kg/day. The verbenone chemotype limits are based on 14.9% camphor and 2.9% isopinocamphone, with limits of 0.24% and 0.1 mg/ kg/day for isopinocamphone.
Regulatory guidelines  Has GRAS status.

Organ-specific effects
Adverse skin reactions  Undiluted rosemary oil was moderately irritating to rabbits; tested at 10% on 25 volunteers it was neither irritating nor sensitizing; it is non-phototoxic. In a study of 200 consecutive dermatitis patients, none were sensitive to 2% rosemary oil on patch testing.

Cardiovascular effects In normal rabbits, 25 mg/kg im rosemary oil produced 20–55% increases in plasma glucose levels after 60–120 minutes, and a 30% decrease in serum insulin levels. In spite of being contraindicated for people with high blood pressure in several aromatherapy books there is no evidence that rosemary oil is hypertensive.

Reproductive toxicity  The low reproductive toxicity of camphor, 1,8-cineole, a-pinene, b-myrcene and (þ)-limonene suggest that most rosemary oils are not hazardous in pregnancy. However, bornyl acetate and verbenone have not been studied.

Systemic effects
Acute toxicity  Rosemary oil acute oral LD50 in rats 5 mL/kg; acute dermal LD50 in rabbits >10 mL/kg. Rosemary oil was not significantly cytotoxic to cultured human umbilical vein endothelial cells. Camphor is potentially neurotoxic and may be more toxic in humans than in rodents. Camphor minimum LD50 is1.7 g/kg in rats. 1,8-Cineole has been reported to cause serious poisoning in young children when accidentally instilled into the nose.

Antioxidant/pro-oxidant activity  Rosemary oil showed high antioxidant activity as a DPPH radical scavenger and against lipid peroxidation. A rosemary oil showed high antioxidant activity in the same two assays.

Carcinogenic/anticarcinogenic potential  Orally administered rosemary oil  was hepatoprotective in rats and antimutagenic in Swiss mice. The antimutagenic dose of 1,100 mg/kg/day for seven days prevented the formation of micronuclei. In a similar study, there was a significant increase in micronuclei in Swiss mice given a single dose of 1,000 or 2,000 mg/kg, but there was no genotoxicity in a group on 300 mg/kg. However, a comet assay found all three doses to be genotoxic. Rosemary oil induced apoptosis in human liver cancer cells.

Drug interactions  Given to male rats in their diet at 0.5% for two weeks, rosemary oil selectively induced CYP2B1 and CYP2B2 in rat liver. This high-dose regimen does not suggest a significant risk of drug interaction.

Many of the above studies do not specify which chemotype was used. Rosemary oil is produced in many parts of the world, and this summary of chemotypes may not represent every type of commercial oil. 1,8-Cineole chemotypes tend to be Moroccan or Tunisian, a-pinene chemotypes are often from Spain bornyl acetate chemotypes may be French, myrcene chemotypes are probably Portuguese and verbenone chemotypes are generally Egyptian. Rosemary oils are also  produced in England, Russia, Germany, Romania and the Balkans. Most research papers do not identify the type of rosemary oil used.

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