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Tinh dầu Cây trinh nữ Địa Trung Hải

Chaste Tree

Vitex agnus castus L.

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Thảo mộc đồi Địa Trung Hải ngập nắng gió, sắc long não mát lạnh vút lên tươi tỉnh, cay nhẹ như hạt tiêu xanh thoảng qua, nhựa cây ấm áp lặng lẽ giữ chân, trong sáng và trầm tĩnh đến lạ

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Tóm Tắt Khoa Học

Từ Thư Viện Kinh Điển
  1. Vitex agnus castus L. (Verbenaceae) — essential oil from leaves OR seeds (two source tissues → two chemotype profiles). Synonym: Monk's pepper. Historically used in traditional medicine for gynecological hormone modulation.
  2. Hazards: Drug interaction + reproductive hormone modulation + may contain methyleugenol (seed oil 0–1.5%).
  3. Contraindications (all routes): progesterone therapy + pregnancy + breastfeeding + prepubertal children. Cautions (all routes): may cause unpleasant side effects in some women.
  4. Cautions (oral): drugs metabolized by CYP2D6 (Appendix B) + estrogen replacement therapy + oral contraceptives. Farnesene + α-bisabolol inhibit CYP2D6 (Ch.14 Table 4.11B).
  5. Dopaminergic mechanism: Stimulates dopamine D2 receptors → suppresses prolactin → lowers FSH/LH/estrogen, raises progesterone. Clinical evidence of symptom exacerbation (emotional decline + hot flashes + breakthrough bleeding) in 23.2% of 52 women at 1.5% topical for 3 months (Lucks 2003). Avoid in pregnancy (Senatore 1996; Zwaving & Bos 1996; Sørensen & Katsiotis 2000).
🌿
Thận trọngNốt TopCamphoraceous-herbal-woody (cineole leaf) or fresh-terpene-herbal (sabinene seed)

Chaste Tree

Tinh dầu Cây trinh nữ Địa Trung Hải (Vitex)

Vitex agnus castus L.

Tinh dầu Cây trinh nữ Địa Trung Hải (Vitex) — Camphoraceous-herbal-woody (cineole leaf) or fresh-terpene-herbal (sabinene seed)

⚠️Tinh dầu này cần thận trọng khi sử dụng. Đọc kỹ hướng dẫn an toàn.

Tổng Quan

Danh pháp khoa học
Vitex agnus castus L.
Họ thực vật
Verbenaceae
Bộ phận dùng
Leaves / Seeds (two source tissues, two chemotype profiles)
Phương pháp chiết xuất
steam_distillation
Màu sắc
Phân loại nốt hương
Nốt Top
Hương thơm
Chemotype / Cultivar

Tình trạng tại Việt Nam

Xem chi tiết

Phân loại nốt
Top
Cường độ
3/5
Độ bền trên da
2–4 giờ
Họ hương
Camphoraceous-herbal-woody (cineole leaf) or fresh-terpene-herbal (sabinene seed)
Hương đầu (Opening)(0–15 phút)

Sun-warmed Mediterranean hillside herbs, crisp camphorous edge sharpening the air, faintly peppery green spice from shadowed seeds, soft resinous warmth rising in the dry-down, clean and quietly medicinal

Hương giữa (Heart)(15–60 phút)

Thảo mộc đồi Địa Trung Hải ngập nắng gió, sắc long não mát lạnh vút lên tươi tỉnh, cay nhẹ như hạt tiêu xanh thoảng qua, nhựa cây ấm áp lặng lẽ giữ chân, trong sáng và trầm tĩnh đến lạ

Hương nền (Drydown)(1–4 giờ)

2–4 giờ

Cường độ hương
3/5
Da khô
2/5

Da dầu/mụn
2/5

Da lão hóa
3/5

Da thường
2/5

Da nhạy cảm
1/5

Da hỗn hợp
2/5

Nhập khẩuImported

Tên gọi tại Việt Nam

Tinh dầu Cây trinh nữ Địa Trung Hải (Vitex)

Pha Chế & Hòa Hợp

Hormonal modulation — progesterone pathway

Topical application at 1.5% demonstrated measurable progesterone-mediated endocrine effects (breakthrough bleeding in 23.2% of subjects), confirming pharmacological activity; evidence reflects adverse disruption rather than validated therapeutic benefit at the studied concentration.

Ref: Lucks (2003) — n=52, 1.5% topical 3-month study; Lucks (2002) — pilot n=23

Anti-inflammatory — cutaneous

α-Bisabolol constituent inhibits inflammatory mediators via mechanisms consistent with its well-documented activity in chamomile EO; CYP2D6 inhibitory profile may additionally modulate metabolism of pro-inflammatory substrates.

Ref: class-extrapolation from German chamomile (α-bisabolol); Tisserand & Young 2014, Ch.14 (α-Bisabolol, Table 4.11B)

Anxiolytic / nervine

Sesquiterpene-rich profile (farnesene, bisabolol) may contribute mild sedative and nervous-system calming effects via olfactory and dermal pathways, consistent with general sesquiterpene class activity across Verbenaceae.

Ref: class-extrapolation from sesquiterpene-class EOs; Tisserand & Young 2014, Ch.13 p.525–527

Antimicrobial — broad spectrum

Monoterpene and sesquiterpene hydrocarbon constituents disrupt microbial membrane integrity; mechanism common across terpene-rich Verbenaceae EOs, though EO-specific MIC data for V. agnus-castus are not cited in the primary source.

Ref: class-extrapolation from Verbenaceae peer EOs; Senatore, Della Porta & Reverchon (1996) — constituent chemistry

CYP2D6 inhibition (pharmacological hazard)

Farnesene and α-bisabolol are documented CYP2D6 inhibitors per T&Y Table 4.11B, affecting metabolism of codeine, tamoxifen, and other CYP2D6 substrates; this is a drug-interaction hazard, not a therapeutic action.

Ref: Tisserand & Young 2014, Ch.14 — Table 4.11B (Farnesene; α-Bisabolol)

AI-summary

Two controlled pilot studies by Lucks examined Vitex agnus-castus EO applied topically. Lucks (2002) — n=23 pilot — documented adverse symptom responses with leaf and seed oil. Lucks (2003) — n=52, 1.5% topical, 3 months — reported 23.2% symptom exacerbation and progesterone breakthrough bleeding, confirming real endocrine activity framed as adverse rather than therapeutic. No positive-outcome RCT for the EO has been located. Caution: extensive phytotherapy evidence for Vitex berry extracts (iridoid-mediated dopaminergic and progesterone receptor activity) is NOT transferable to the steam-distilled EO; iridoid glycosides are non-volatile and absent from the distillate.

Narrative

Tâm trạng: Balancing, Calming

clarityrestraintbalancefocusrenewalequanimity

Chakra

sacral

Ngũ hành

moc

Phương phápLiều lượngGhi chú
Diffusion2–3 drops in 100 ml water or 3–4 drops per 30-min sessionSafest route — avoids dermal methyleugenol exposure. Use for emotional support, cycle-associated stress, or nervine calming. Contraindicated in rooms occupied by pregnant women or children under 12.
Topical massage — abdomen / lower back1.0–1.3% in carrier oil; strict adult max 1.3%; lower dilution preferredApply to lower abdomen or sacral area for menstrual discomfort. Strictly avoid pregnancy and children under 12. Discontinue if breakthrough bleeding occurs. Patch-test 48 h prior.
Topical spot application — pulse points0.5–1.0% in jojoba or fractionated coconut oilWrists, temples, or back of neck for inhalation-combined benefit. Conservative dilution mandatory: methyleugenol IFRA leave-on cap 0.0004% (IFRA 2009), 0.0002% (European Commission 2002).
Personal inhaler (nasal stick)4–6 drops on cotton wickOn-demand inhalation for PMS emotional symptoms or stress. No carrier needed. Do not share with pregnant users. Replace wick every 2–3 weeks.

Dầu nền phù hợp

Jojoba oilLiquid wax, near-zero comedogenic rating; stable shelf life minimizes methyleugenol oxidation risk; suits hormonal-skin blends and abdominal massage without adding sensitization load.
Fractionated coconut oilOdorless and very stable — ideal neutral carrier for this pharmacologically active EO; minimizes carrier-side variables; good absorption for abdominal or lower-back application.
Sweet almond oilGentle medium-viscosity carrier for body massage; adds mild skin-conditioning effect; low sensitization potential appropriate given EO's existing methyleugenol sensitization risk.

Kết hợp tốt với

CamphoraceousSpicyWoodyCitrusGreen

Blend kinh điển

[Tisserand & Young] Ch.13 p.525–527 (Chaste tree)
[Senatore, Della Porta & Reverchon] chemistry, leaf + seed
[Valentini, Bellomaria, Arnold & Arnold] chemistry
[Sørensen & Katsiotis] chemistry, methyleugenol-bearing chemotype
[Lucks] pilot study n=23, leaf + seed oil adverse symptoms
[Zwaving & Bos] chemistry
[Chapter 14 Constituent profiles] Methyleugenol (rodent carcinogen), Farnesene + α-Bisabolol (CYP2D6 inhibitors Table 4.11B)
[IFRA] methyleugenol 0.0004% leave-on
[European Commission] SCCNFP methyleugenol 0.0002% leave-on

An Toàn

Giới hạn da tối đa

Xem chi tiết

Giới hạn IFRA

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Thai kỳ & Cho con bú

Tam cá nguyệt 1Unknown
Tam cá nguyệt 2Unknown
Tam cá nguyệt 3Unknown

Giới hạn độ tuổi

Xem chi tiết

Bảo quản

Bảo quản nơi tối, mát

Thông tin chỉ mang tính tham khảo, không thay thế tư vấn y tế chuyên nghiệp. SYMELab v2.0

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Hồ Sơ Hoá Học Chi Tiết
§3 Chemical Profile — chemotype, constituent ranges, adulteration

Leaf oil — Senatore et al 1996; Valentini et al 1998

ConstituentRange
1,8-Cineole15.6–35.2%
Sabinene6.9–17.1%
α-Pinene1.0–13.9%
α-Terpineol1.4–9.2%
γ-Elemene0–9.1%
β-Selinene0–9.0%
β-Caryophyllene2.3–8.9%
(Z)-β-Farnesene0–8.6%
Citronellyl acetate0.3–7.8%
Citronellic acid0–6.6%
(+)-Limonene0.1–4.1%
Terpinen-4-ol1.4–3.7%
β-Myrcene0–3.5%
α-Bisabolol0–2.7%
(E)-β-Farnesene0–2.6%
(E)-Nerolidol0–2.5%
β-Pinene1.4–2.4%
(Z)-β-Ocimene0.01–2.2%
(−)-allo-Aromadendrene0–2.0%
Spathulenol0.4–1.8%
(E)-Dihydroterpineol0–1.8%
γ-Terpinene0.8–1.6%
α-Gurjunene0.4–1.6%
Guaiol0–1.3%
Manool0–1.3%
α-Guaiene0–1.2%
T-Cadinol0–1.2%
Dodecane0–1.0%
Thymol0–1.0%

Seed oil — Senatore et al 1996; Valentini et al 1998; Sørensen & Katsiotis 2000

ConstituentRange
Sabinene7.1–44.1%
1,8-Cineole8.4–23.3%
α-Pinene1.2–23.1%
γ-Elemene0–17.0%
(E)-β-Farnesene0–10.3%
β-Caryophyllene0.8–9.3%
α-Terpineol0.2–9.3%
(+)-Limonene0.5–7.4%
(Z)-β-Farnesene0–6.9%
Citronellyl acetate0.2–6.0%
β-Selinene0–6.0%
β-Myrcene0–5.6%
α-Terpinyl acetate0.1–4.6%
Linalyl acetate0–3.6%
Linalool0–3.0%
Thymol0–2.7%
Caryophyllene oxide0–2.5%
Terpinen-4-oltr–2.2%
(−)-allo-Aromadendrene0–2.1%
Spathulenol0.2–2.0%
α-Bisabolol0–1.8%
γ-Terpinene0.5–1.7%
T-Cadinol0–1.6%
β-Pinene0.8–1.5%
Methyleugenol0–1.5%
(E)-Dihydroterpineol0–1.3%
α-Gurjunene0–1.2%
Piperitone0–1.2%
Citronellol0.2–1.0%
α-Guaiene0–1.0%
Guaiol0–1.0%
(Z)-β-Ocimene0–1.0%
Germacrene D0–1.0%

Chemistry insights

  • Leaf vs seed distinction: Leaf oil is 1,8-cineole-dominant (15.6–35.2%) with oxide-heart; seed oil is sabinene-dominant (7.1–44.1%) with monoterpene-hydrocarbon-heart. Both share α-pinene + β-caryophyllene + α-terpineol in similar ranges.
  • Methyleugenol 0–1.5% in SEED oil (absent or trace in leaf per the tables): This is the regulatory flag for seed oil specifically. Worst-case 1.5% × 0.02% methyleugenol dermal limit → practical cap 1.3% for seed oil on methyleugenol basis alone — but the hormone contraindication overrides this.
  • Farnesene + α-bisabolol: CYP2D6 inhibitors per Ch.14 Table 4.11B — drug interaction rail (oral route).
  • Dopaminergic mechanism (whole oil): Alcoholic extracts of V. agnus castus plant stimulate dopamine D2 receptors → dopamine suppresses prolactin → altered FSH/LH/estrogen/progesterone balance. Mechanism documented in traditional + biomedical literature.
Công Dụng Trị Liệu Chi Tiết
§10 Therapeutic Uses — skin, emotional, physical, respiratory
  • Traditional / modern niche: Premenstrual syndrome (PMS), menstrual irregularity, corpus luteum insufficiency, amenorrhea, hyperprolactinemia — via dopamine D2 agonism → prolactin suppression → FSH/LH/estrogen/progesterone balance shift.
  • Formulations: Typically used as chaste tree fruit extract (tincture) in herbal medicine — NOT as essential oil — for these applications. Essential oil use is much rarer and the Lucks 2002/2003 studies suggest topical essential oil may cause symptom exacerbation rather than relief in some women.
  • Male use: Traditional "chaste tree" monastic context — claimed libido suppression via hormone modulation; biomedical evidence limited.
  • Aromatherapy use — with caution: Only for non-pregnant, non-lactating, post-pubertal adults. Patch-test. Avoid concurrent progesterone (cream, tablets, injections). Consider the Lucks 2003 23.2% adverse-symptom rate when evaluating risk/benefit.
Năng Lượng & Ngũ Hành
§11 Energetics — TCM, Ayurveda, aromatic energetics
  • Five-element: Mộc (Wood — menstrual/reproductive-cycle resonance; Liver-meridian context in TCM-inspired frameworks).

Dữ Liệu Kỹ Thuật Y Khoa

§14 Renderer Contract — Tisserand & Young V2.2

Thông Số Định Lượng

hazards
["drug_interaction_cyp2d6","reproductive_hormone_modulation","methyleugenol_seed_oil","clinical_symptom_exacerbation_lucks_2003"]
phototoxic
false
safety_level
caution
cap_derivation
methyleugenol_seed_1.5pct_plus_hormone_contraindication
oxidation_risk
medium
drug_interactions
["cyp2d6_inhibitor","progesterone_therapy","estrogen_replacement_therapy","oral_contraceptives"]
shelf_life_months
24
max_dilution_adult
1.3
contraindicated_all
false
max_dilution_elderly
1.3
max_oral_dose_mg_day
max_dilution_child_2_6
0
max_dilution_sensitive
1
max_dilution_adult_face
1
max_dilution_child_6_12
0
contraindicated_children
true
contraindicated_pregnancy
true
max_dilution_child_under2
0
max_dilution_pregnancy_1st
0
max_dilution_pregnancy_2nd
0
max_dilution_pregnancy_3rd
0

Tài Liệu Y Khoa Tham Khảo

  • Tisserand & Young (2014) Essential Oil Safety 2nd ed — Ch.13 p.525–527 (Chaste tree)
  • Senatore, Della Porta & Reverchon (1996) — chemistry, leaf + seed
  • Valentini, Bellomaria, Arnold & Arnold (1998) — chemistry
  • Sørensen & Katsiotis (2000) — chemistry, methyleugenol-bearing chemotype
  • Lucks (2002) — pilot study n=23, leaf + seed oil adverse symptoms
  • Lucks (2003) — main study n=52, 1.5% topical 3 months, 23.2% symptom exacerbation + progesterone breakthrough bleeding
  • Zwaving & Bos (1996) — chemistry
  • Chapter 14 Constituent profiles — Methyleugenol (rodent carcinogen), Farnesene + α-Bisabolol (CYP2D6 inhibitors Table 4.11B)
  • IFRA (2009) — methyleugenol 0.0004% leave-on
  • European Commission (2002) — SCCNFP methyleugenol 0.0002% leave-on