Blue Chamomile

Matricaria recutita

Chemotype: bisabolol oxide / beta-farnesene / chamazulene type

sweetfruityherbaceous

PLANT PART: flowers and buds
EXTRACTION: steam distillation
AROMA NOTE: mid

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LEARN AS YOU COMPARE

What’s inside this oil?

Constituents are the natural chemicals that give an oil its character. See the main ones, learn what they do, and explore differences between batches.

I’m interested in

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FOLLOW YOUR SENSES

Aroma & character

A closer look at this oil's scent, strength, and staying power.

sweetfruityherbaceous

Aroma intensity: 50 / 100

Soft & subtleBold & expressive

Note layer: mid

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A LITTLE CARE GOES A LONG WAY

Using it thoughtfully

Read the full safety context before bringing this oil into your routine.

Cited dermal maximum · leave-on: 4%
Phototoxicity: Not flagged in this profile
Oxidation risk: medium

A cited maximum is a limit, not a suggested dilution. Missing restrictions do not establish safety.

No furocoumarin-driven phototoxic restriction was identified for the steam-distilled flower oil in the consulted sources.

Contraindications & cautions

moderateA public AromaWeb safety summary citing Tisserand and Young states that German chamomile oil may interact with drugs metabolized by CYP2D6.
moderatePatch-test literature reviewed by CIR found positive reactions in a minority of sensitized patients, so Asteraceae-sensitive users should use caution.

Read the complete safety guide

Explore measured chemistry from supplier batches

A supplier report describes a particular sample. Open this workspace to investigate measured constituents and their original documents.

THE SCIENCE BEHIND THE SCENT

Inside the oil

26 constituents

An oil's character comes from its natural chemical composition. Explore each constituent to understand the connections.

About this composition

Public composition sources for German blue chamomile vary between beta-farnesene-rich and bisabolol-oxide-rich lots, but they consistently place bisabolol oxides, beta-farnesene, chamazulene, alpha-bisabolol, bisabolone oxide A, and spiroether/en-yn-dicycloether among the major constituents. This record anchors the quantitative profile to the open Estonian GC/FID-GC/MS paper, then cross-checks the broad German-chamomile pattern against current public supplier summaries.

Constituent	Typical amount	Reported range	Chemical family	Source
alpha-Bisabolol oxide A	26.5%	20–33%	sesquiterpene oxide	View source Volatile Constituents of Matricaria recutita L. from Estonia; alpha-bisabolol oxide A entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (pp.1,6 / lines 9-12 and 198-200: bisabolol oxide A 20-33%); https://www.thegoodscentscompany.com/data/rw1445511.html (CAS 22567-36-8)
en-yn-dicycloether (spiroether)	19.5%	17–22%	spiroether	View source Volatile Constituents of Matricaria recutita L. from Estonia; trans-spiroether entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (pp.1,6 / lines 11-12 and 199-200: en-yn-dicycloether 17-22%); https://www.thegoodscentscompany.com/data/rw1560291.html ((E)-en-yn-dicycloether synonym / no CAS listed)
(E)-beta-Farnesene	8.5%	4–13%	sesquiterpene hydrocarbon	View source Volatile Constituents of Matricaria recutita L. from Estonia; (E)-beta-farnesene entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (pp.1,6 / lines 10-11 and 198-199: (E)-beta-farnesene 4-13%); https://www.thegoodscentscompany.com/data/rw1053891.html (CAS 18794-84-8)
alpha-Bisabolol	5.5%	3–8%	sesquiterpene alcohol	View source Volatile Constituents of Matricaria recutita L. from Estonia; alpha-bisabolol entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (p.6 / lines 198-199: alpha-bisabolol 3-8%); https://webbook.nist.gov/cgi/cbook.cgi?ID=C515695&Mask=200 (CAS 515-69-5)
Chamazulene	6%	5–7%	sesquiterpene hydrocarbon	View source Volatile Constituents of Matricaria recutita L. from Estonia; Chamazulene entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (pp.1,6 / lines 11-12 and 199-204: chamazulene 5-7%); https://comptox.epa.gov/dashboard/chemical/synonyms/DTXSID70200939 (CAS 529-05-5)
alpha-Bisabolone oxide A	10.5%	7–14%	sesquiterpene oxide	View source Volatile Constituents of Matricaria recutita L. from Estonia; alpha-bisabolone oxide A entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (pp.1,6 / lines 10-11 and 198-199: bisabolone oxide A 7-14%); https://www.arctomsci.com/hy-n8120-1 (CAS 22567-38-0)
alpha-Bisabolol oxide B	10%	8–12%	sesquiterpene oxide	View source Volatile Constituents of Matricaria recutita L. from Estonia; alpha-bisabolol oxide B entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (pp.1,6 / lines 10-11 and 198-199: bisabolol oxide B 8-12%); https://www.thegoodscentscompany.com/data/rw1467641.html (CAS 26184-88-3)
Spathulenol	3.03%	2.3–3.6%	oxygenated sesquiterpene alcohol	View source Volatile Constituents of Matricaria recutita L. from Estonia; Spathylenol entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: Spathylenol 3.6/2.3/3.2% for Samples 1/2/3, mean 3.03%); https://pubchem.ncbi.nlm.nih.gov/compound/Spathulenol (CAS 6750-60-3)
Decanoic acid	1.63%	1.1–2.1%	saturated fatty acid	View source Volatile Constituents of Matricaria recutita L. from Estonia; Decanoic acid entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: Decanoic acid 2.1/1.1/1.7% for Samples 1/2/3, mean 1.63%); https://pubchem.ncbi.nlm.nih.gov/compound/Decanoic-acid (CAS 334-48-5)
Germacrene D + gamma-Muurolene (combined peak)	0.93%	0.5–1.7%	sesquiterpene hydrocarbon	View source Volatile Constituents of Matricaria recutita L. from Estonia; Germacrene D / gamma-Muurolene combined entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: Germacrene D + gamma-Muurolene reported as one co-eluting peak, 1.7/0.6/0.5% for Samples 1/2/3, mean 0.93%); https://www.thegoodscentscompany.com/data/rw1007561.html (Germacrene D, CAS 23986-74-5); https://www.thegoodscentscompany.com/data/rw1465981.html (gamma-Muurolene, CAS 30021-74-0)
alpha-Farnesene	0.53%	0.3–0.9%	sesquiterpene hydrocarbon	View source Volatile Constituents of Matricaria recutita L. from Estonia; alpha-Farnesene entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: alpha-Farnesene 0.9/0.4/0.3% for Samples 1/2/3, mean 0.53%); https://www.thegoodscentscompany.com/data/rw1000221.html (CAS 502-61-4)
beta-Caryophyllene	0.1%	0.1–0.1%	sesquiterpene hydrocarbon	View source Volatile Constituents of Matricaria recutita L. from Estonia; beta-Caryophyllene entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: beta-Caryophyllene 0.1% across all three samples); https://www.thegoodscentscompany.com/data/rw1005771.html (CAS 87-44-5)
beta-Bisabolene	0.28%	0.05–0.7%	sesquiterpene hydrocarbon	View source Volatile Constituents of Matricaria recutita L. from Estonia; beta-Bisabolene entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: beta-Bisabolene 0.7% (Sample 1), trace (<0.05%, Sample 2), 0.1% (Sample 3), mean 0.28%); https://www.thegoodscentscompany.com/data/rw1004651.html (CAS 495-61-4)
Artemisia ketone	0.33%	0.2–0.4%	monoterpene ketone	View source Volatile Constituents of Matricaria recutita L. from Estonia; Artemisia ketone entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: Artemisia ketone 0.2/0.4/0.4% for Samples 1/2/3, mean 0.33%); https://www.thegoodscentscompany.com/data/rw1003211.html (CAS 546-49-6)
Caryophyllene oxide	0.12%	0.05–0.2%	oxygenated sesquiterpene	View source Volatile Constituents of Matricaria recutita L. from Estonia; Caryophyllene oxide entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: Caryophyllene oxide trace(<0.05%)/0.2/0.1% for Samples 1/2/3, mean 0.12%); https://www.thegoodscentscompany.com/data/rw1005791.html (CAS 1139-30-6)
tau-Cadinol	0.2%	0.2–0.2%	sesquiterpene alcohol	View source Volatile Constituents of Matricaria recutita L. from Estonia; T-Cadinol entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: T-Cadinol 0.2% across all three samples); https://www.thegoodscentscompany.com/data/rw1493741.html (tau-Cadinol, CAS 5937-11-1)
(E)-Nerolidol	0.1%	0.1–0.1%	sesquiterpene alcohol	View source Volatile Constituents of Matricaria recutita L. from Estonia; (E)-Nerolidol entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: (E)-Nerolidol 0.1% across all three samples); https://www.thegoodscentscompany.com/data/rw1053871.html (CAS 7212-44-4)
Sabinene	0.08%	0.05–0.1%	monoterpene hydrocarbon	View source Volatile Constituents of Matricaria recutita L. from Estonia; Sabinene entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: Sabinene trace(<0.05%)/0.1/0.1% for Samples 1/2/3); https://www.thegoodscentscompany.com/data/rw1444601.html (CAS 3387-41-5)
Myrcene	0.08%	0.05–0.1%	monoterpene hydrocarbon	View source Volatile Constituents of Matricaria recutita L. from Estonia; Myrcene entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: Myrcene trace(<0.05%)/0.1/0.1% for Samples 1/2/3); https://www.thegoodscentscompany.com/data/rw1053241.html (CAS 123-35-3)
p-Cymene	0.07%	0.05–0.1%	monoterpene hydrocarbon	View source Volatile Constituents of Matricaria recutita L. from Estonia; p-Cymene entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: p-Cymene trace(<0.05%)/trace(<0.05%)/0.1% for Samples 1/2/3); https://www.thegoodscentscompany.com/data/rw1053741.html (CAS 99-87-6)
gamma-Terpinene	0.08%	0.05–0.1%	monoterpene hydrocarbon	View source Volatile Constituents of Matricaria recutita L. from Estonia; gamma-Terpinene entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: gamma-Terpinene trace(<0.05%)/0.1/0.1% for Samples 1/2/3); https://www.thegoodscentscompany.com/data/rw1053081.html (CAS 99-85-4)
Terpinolene	0.08%	0.05–0.1%	monoterpene hydrocarbon	View source Volatile Constituents of Matricaria recutita L. from Estonia; Terpinolene entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: Terpinolene trace(<0.05%)/0.1/0.1% for Samples 1/2/3); https://www.thegoodscentscompany.com/data/rw1055011.html (CAS 586-62-9)
(E)-beta-Ocimene	0.08%	0.05–0.1%	monoterpene hydrocarbon	View source Volatile Constituents of Matricaria recutita L. from Estonia; (E)-beta-Ocimene entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: (E)-beta-Ocimene trace(<0.05%)/0.1/0.1% for Samples 1/2/3); https://www.thegoodscentscompany.com/data/rw1560331.html (CAS 3779-61-1)
Cadinene isomers (gamma- and delta-cadinene)	0.1%	0.05–0.2%	sesquiterpene hydrocarbons	View source Volatile Constituents of Matricaria recutita L. from Estonia; gamma-Cadinene / delta-Cadinene entries https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: gamma-Cadinene 0.1%/trace/trace and delta-Cadinene 0.1%/trace/trace for Samples 1/2/3, combined mean approx. 0.1%)
Terpinen-4-ol	0.07%	0.05–0.1%	monoterpene alcohol	View source Volatile Constituents of Matricaria recutita L. from Estonia; Terpinen-4-ol entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: Terpinen-4-ol trace(<0.05%)/0.1/trace(<0.05%) for Samples 1/2/3); https://www.thegoodscentscompany.com/data/rw1054971.html (CAS 562-74-3)
alpha-Terpineol	0.07%	0.05–0.1%	monoterpene alcohol	View source Volatile Constituents of Matricaria recutita L. from Estonia; alpha-Terpineol entry https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf (Table 2, p.43: alpha-Terpineol trace(<0.05%)/0.1/trace(<0.05%) for Samples 1/2/3); https://www.thegoodscentscompany.com/data/rw1055301.html (CAS 98-55-5)

Profile source: Volatile Constituents of Matricaria recutita L. from Estonia; German Chamomile Essential Oil profile (AromaWeb); Chamomile German Essential Oil (Hungary) (New Directions Aromatics) · https://kirj.ee/wp-content/plugins/kirj/pub/chem-1-2001-39-45_20230303105939.pdf ; https://www.aromaweb.com/essential-oils/german-chamomile-essential-oil.php ; https://www.newdirectionsaromatics.com/oils/essential-oils/chamomile-german-essential-oil-hungary

A TRADITION OF BOTANICAL CURIOSITY

Traditional & reported uses

These uses reflect the profile's reported traditions and literature. They are not established treatment recommendations.

traditionally used in aromatherapy for calming and relaxation
reported to support easing of occasional skin irritation and redness in topical blends
used in massage blends for soothing muscle and joint comfort
traditionally associated with easing occasional tension and promoting restful sleep
used in skincare formulations for its calming, azulene-blue reputation

Explore related intentionsSleep & Rest ↗Relaxation & Calming ↗Stress Relief ↗

For aromatherapy and wellness use only — not medical advice. Effect statements are traditional/reported associations, not treatment claims. The Synergy Rating scores blend craft, harmony and safety, not medical efficacy. Read the safety framework.

What we're still learning · 5 data gaps

Good decisions start with knowing what is — and isn't — in the evidence.

The public 4% max dermal figure used here comes from a live secondary compilation that explicitly attributes its chamomile maximum dilution list to Tisserand and Young; a directly inspectable primary/public profile page from Tisserand or IFRA was not available in this pass.
No public source reviewed in this pass provided a native 0-100 odor-intensity score; the stored value normalizes qualitative aroma-strength language from public profiles.
No public source reviewed in this pass provided verified volatility-rate data.
No open chemical registry with a confirmed CAS number was verified for the generic combined en-yn-dicycloether entry, so CAS remains null instead of guessed.
Closure raised from 0.865 to 0.9446 by adding all remaining GC/MS-identified minor constituents from the Estonia Table 2 source (Orav et al. 2001); the paper totals only 97-99% per sample with ~1-3% left as chromatographically unidentified peaks, so 0.95 could not be reached without inventing unsupported figures.