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Tinh dầu hạt thì là đen / hắc chủng thảo

Black Seed

Nigella sativa L.

TopGia vị

Cay hắc y dược bốc nhiệt đắng sắc, ấm nồng phenolic như cỏ xạ hương khô phơi nắng sa mạc, khói đất cằn quyện giữa cay sắc, xâm lấn quyết đoán, hơi ấm cổ xưa vương vấn lâu không tan

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Tóm Tắt Khoa Học

Từ Thư Viện Kinh Điển
  1. Nigella sativa L. (Ranunculaceae) — hạt (seeds), steam-distilled essential oil. Tên gọi đa dạng — đặc biệt cảnh báo nhầm lẫn với "black seed FIXED OIL" (cold-pressed lipid extract, vẫn bán dưới cùng tên thương mại "black seed oil" / "kalonji oil"). Fixed oil chứa ~0.5% essential oil → toxicology overlap.
  2. Primary hazard = thymoquinone-driven fetotoxicity + skin sensitization (moderate) + drug interaction (antidiabetic). Thymoquinone 26.8–54.8% là constituent dominant + signature anti-inflammatory + lý do contraindication.
  3. Chemistry: Thymoquinone 26.8–54.8% + p-cymene 14.7–38.0% + longifolene 1.2–10.2% + α-thujene 1.3–10.1% + carvacrol 0.5–4.2%. Mozaffari et al 2000 (Iranian seeds, steam distilled). Microwave-distilled oils có thymoquinone 6.2–18.4% — chemotype variation đáng kể giữa countries.
  4. Contraindicated pregnancy + breastfeeding (all routes). Cautions: oral với antidiabetic medication (cardiovascular hypoglycemic effect); dermal trên hypersensitive/diseased/damaged skin + children under 2 years.
  5. Non-phototoxic (Ranunculaceae seed steam EO ≠ furocoumarin source). Skin sensitization moderate — multiple ACD case reports (5+ confirmed in literature 1995–2012). Disambiguate carefully từ FIXED OIL khi lấy lịch sử bệnh nhân.
🌿
Thận trọngNốt TopPhenolic-spicy-medicinal (thymol-cousin, peppery, slightly bitter-resinous)

Black Seed

Tinh dầu hạt thì là đen / hắc chủng thảo (Black seed / Black cumin)

Nigella sativa L.

Tinh dầu hạt thì là đen / hắc chủng thảo (Black seed / Black cumin) — Phenolic-spicy-medicinal (thymol-cousin, peppery, slightly bitter-resinous)

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

Tổng Quan

Danh pháp khoa học
Nigella sativa L.
Họ thực vật
Ranunculaceae
Bộ phận dùng
Seeds
Phương pháp chiết xuất
steam_distillation
Màu sắc
Phân loại nốt hương
Nốt Top
Hương thơm
Chemotype / Cultivar

Tình trạng tại Việt Nam

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Phân loại nốt
Top
Cường độ
4/5
Độ bền trên da
2–4 giờ
Họ hương
Phenolic-spicy-medicinal (thymol-cousin, peppery, slightly bitter-resinous)
Hương đầu (Opening)(0–15 phút)

Pungent medicinal heat with bitter edge, wild phenolic warmth of sun-scorched thyme and cumin, dry-earth smoke threaded through sharp spice, assertive and penetrating, an ancient fieriness that lingers long

Hương giữa (Heart)(15–60 phút)

Cay hắc y dược bốc nhiệt đắng sắc, ấm nồng phenolic như cỏ xạ hương khô phơi nắng sa mạc, khói đất cằn quyện giữa cay sắc, xâm lấn quyết đoán, hơi ấm cổ xưa vương vấn lâu không tan

Hương nền (Drydown)(1–4 giờ)

2–4 giờ

Cường độ hương
4/5
Da khô
2/5

Da dầu/mụn
3/5

Da lão hóa
2/5

Da thường
3/5

Da nhạy cảm
1/5

Da hỗn hợp
3/5

Nhập khẩuImported

Tên gọi tại Việt Nam

Tinh dầu hạt thì là đen / hắc chủng thảo (Black seed / Black cumin)

Pha Chế & Hòa Hợp

Antioxidant

Thymoquinone (26.8–54.8% of EO) directly scavenges reactive oxygen species and inhibits lipid peroxidation, reducing oxidative damage at the cellular level.

Ref: Burits & Bucar (2000); Hosseinzadeh et al (2007); Abdel-Wahhab & Aly (2005)

Anti-inflammatory (topical, preclinical)

Thymoquinone modulates the arachidonic acid cascade, suppressing pro-inflammatory eicosanoid synthesis; topical bioavailability from the steam-distilled EO has not been directly measured in human studies.

Ref: Tisserand & Young 2014, Ch.13

Antimicrobial

Thymoquinone and p-cymene disrupt microbial cell membrane integrity; both constituents have independently established broad-spectrum antimicrobial activity documented in constituent-level literature.

Ref: Tisserand & Young 2014, Ch.13

Antiproliferative (in vitro / animal models)

Thymoquinone exerts antiangiogenic effects and inhibits tumor cell proliferation in murine models and colon/stomach cell lines; no direct clinical evidence for aromatherapy EO use.

Ref: Yi et al (2008); Salim & Fukushima (2003); Ait M'barek et al (2007a)

Hepatoprotective (animal model)

Thymoquinone-driven reduction of hepatic oxidative stress markers in animal models; route of administration in all cited studies was oral/systemic, not topical EO application.

Ref: Turkdogan et al (2003)

Emmenagogue / uterotonic (traditional, precautionary)

Traditional classification as a post-partum uterine herb; in vitro smooth muscle data are equivocal, but pregnancy contraindication is maintained as an absolute precautionary measure based on historical use.

Ref: Kapur (1948); Aqel & Shaheen (1996)

AI-summary

No RCT-grade clinical evidence exists for the steam-distilled EO in topical or inhalation aromatherapy. Preclinical evidence supports antioxidant activity of dominant constituent thymoquinone via free-radical scavenging and lipid peroxidation inhibition (Burits & Bucar 2000; Hosseinzadeh et al 2007). Antiproliferative and antiangiogenic effects of thymoquinone are documented in murine models and cell lines (Yi et al 2008; Salim & Fukushima 2003), but these studies used isolated constituent or fixed oil administered systemically — not the steam-distilled EO topically. Conversely, clinical evidence of skin sensitization is robust: multiple independent ACD case reports (El-Rab & Al-Sheikh 1995; Zedlitz et al 2002; Steinmann et al 1997) and bullous/EM eruption cases (Nosbaum et al 2011; Gelot et al 2012) confirm the oil as a verified contact allergen requiring mandatory patch testing before any topical use.

Narrative

Tâm trạng: Stimulating, Grounding

resilienceprotectionvitalityfocuscouragepurification

Chakra

solar

Ngũ hành

kim

Phương phápLiều lượngGhi chú
Diffusion2-3 drops in 100 ml diffuser waterLowest-risk route. Use in well-ventilated space, max 30 min per session. Avoid in presence of pregnant women. Intense spicy-medicinal aroma; blend with frankincense or sandalwood to moderate.
Topical massage0.5–1% in carrier oil (max 1% adult dermal cap)Mandatory 48h patch test at 0.5% before first use. Do not exceed 1% dermal cap. Avoid on broken or sensitized skin. Absolutely contraindicated in pregnancy at any dilution. Not for children.
Skincare — spot treatment0.5% in unscented cream or jojoba waxPatch test mandatory. Apply to localized oily or blemish-prone areas only; avoid large facial surfaces. Discontinue immediately at first sign of redness, itching, or swelling.
Steam inhalation1–2 drops in bowl of 500 ml hot waterKeep eyes closed during inhalation. Inhale max 5–10 min. Useful for upper respiratory congestion. Avoid for pregnant women and young children. Not a substitute for medical treatment.

Dầu nền phù hợp

Jojoba waxNon-comedogenic and highly stable; ideal for oily or blemish-prone skin applications; long shelf life complements the need for stable dilution of this sensitizer-risk EO.
Argan oilRich in oleic acid and tocopherols; antioxidant profile synergizes with thymoquinone's antioxidant action and adds emollient benefit within the strict 1% EO cap.
Sweet almond oilMild, versatile carrier with low sensitization potential; reduces compounded allergen burden when diluting a documented contact sensitizer such as black seed EO.
Hemp seed oilHigh linoleic acid content suits oily or acne-prone applications; its own anti-inflammatory fatty acid profile complements the EO's anti-inflammatory constituent actions.

Kết hợp tốt với

SpicyHerbaceousWoodyEarthyResinous

Blend kinh điển

[Tisserand & Young] Ch.13 p.478–479 (Black seed)
[Mozaffari, F. S. et al] chemistry profile (Iranian steam-distilled)
[Lawrence, B. M.] chemotype variation across countries (microwave-distilled)
[El-Rab, M. O. G. & Al-Sheikh, O. A.] 2 dermatitis cases Saudi Arabia
[Zedlitz, S. et al] ACD case report (eczema patient)
[Steinmann, A. et al] ACD case report (28-y-old man)
[Nosbaum, A. et al] erythema multiforme (oral capsules — fixed oil)
[Gelot, P. et al] bullous eruption (oral + dermal)
[Aqel, M. & Shaheen, R.] uterine smooth muscle spontaneous contraction inhibition
[Yi, T. et al] antiangiogenic action of thymoquinone
[Salim, E. I. & Fukushima, S.] DMH-colon antiproliferative
[Ait M'barek, L. et al] antitumor mouse models
[Islam, S. N. et al] immunotoxicity rats + cytotoxicity stomach cell lines
[Sultan, M. T. et al] subchronic toxicity 8-week dietary
[Turkdogan, M. K. et al] hepatoprotective
[Burits, M. & Bucar, F.] antioxidant
[Hosseinzadeh, H. et al] lipid peroxidation protection
[Abdel-Wahhab, M. A. & Aly, S. E.] aflatoxin protection
[Al-Hader, A. et al] hypoglycemic effect rabbits
[Kapur, R.] uterine herb survey post-childbirth
[Badary, O. A. et al] thymoquinone oral LD50 mice
[Jenner, P. M. et al] p-cymene oral LD50 rats

An Toàn

Giới hạn da tối đa

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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

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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

Essential oil — Mozaffari et al 2000 (Iranian, steam-distilled)

Constituent% range
Thymoquinone26.8–54.8%
p-Cymene14.7–38.0%
Longifolene1.2–10.2%
α-Thujene1.3–10.1%
Carvacrol0.5–4.2%
α-Cubebene0.4–3.0%
α-Pinene0.2–2.4%
(+)-Limonene0.7–2.3%
β-Pinene0.4–3.0%
Sabinene0.2–1.6%

Chemistry insights

  • Thymoquinone signature. Same para-quinone class as in select Thymus + Monarda chemotypes. Anti-inflammatory + antitumor + anticonvulsant pharmacology — but ALSO key cytotoxin + contact allergen.
  • Chemotype variation by country (huge): Microwave-distilled oils from 5 countries (Lawrence 2008) — thymoquinone range 6.2–18.4%. Iranian steam-distilled = highest thymoquinone (clinical-grade). Low-thymoquinone chemotypes commercially available BUT therapeutically less valuable.
  • p-Cymene + carvacrol pair — phenolic-monoterpene class shared with Oregano/Thyme; contributes irritation potential.
  • Longifolene 1.2–10.2% — sesquiterpene shared class with Cedarwood Chinese (autoxidation potential noted in T&Y).
  • α-Thujene (NOT thujone) — α-pinene-class isomer, low toxicity.
Công Dụng Trị Liệu Chi Tiết
§10 Therapeutic Uses — skin, emotional, physical, respiratory
  • Anti-inflammatory + immunomodulatory (thymoquinone signature) — significant body of preclinical evidence.
  • Respiratory: Inhaled thymoquinone aerosol dose-dependently protected guinea pigs against histamine-stimulated bronchospasm. Asthma + bronchitis protocols (oral + inhalation, MEDICAL SUPERVISION).
  • Antioxidant: Effective OH radical scavenger (Burits & Bucar 2000), protects against lipid peroxidation (Hosseinzadeh et al 2007), aflatoxin-protective (Abdel-Wahhab & Aly 2005).
  • Hepatoprotective: Injected EO offered protection against induced hepatotoxicity in rats (Turkdogan et al 2003).
  • Anticancer (research-stage): Antiproliferative DMH-colon carcinogenesis model; antitumor mouse models. NOT a primary clinical indication.
  • Traditional Islamic medicine ("habba al-barakah"): Wide-spectrum tonic — fixed oil + seed powder dominate use over EO.
Năng Lượng & Ngũ Hành
§11 Energetics — TCM, Ayurveda, aromatic energetics
  • Five-element: Hỏa (Fire — phenolic-warming + antimicrobial) + Thổ (Earth — seed/grounding + digestive).
  • Mojay: Not in standard Mojay materia medica (more documented in Unani/TCM/Ayurvedic frameworks).
  • Yang-warming, drying, dispersing — phenolic class.

Dữ Liệu Kỹ Thuật Y Khoa

§14 Renderer Contract — Tisserand & Young V2.2

Thông Số Định Lượng

hazards
["fetotoxic","skin_sensitization_moderate","drug_interaction"]
phototoxic
false
cap_derivation
framework_thymoquinone_sensitization
oxidation_risk
medium
drug_interactions
["antidiabetic"]
shelf_life_months
24
max_dilution_adult
1
contraindicated_all
false
max_dilution_elderly
1
max_dilution_child_2_6
0.5
max_dilution_sensitive
0.25
max_dilution_adult_face
0.5
max_dilution_child_6_12
0.5
contraindicated_children
false
contraindicated_pregnancy
true
max_dilution_child_under2
max_dilution_pregnancy_1st
max_dilution_pregnancy_2nd
max_dilution_pregnancy_3rd

Tài Liệu Y Khoa Tham Khảo

  • Tisserand & Young (2014) Essential Oil Safety 2nd ed — Ch.13 p.478–479 (Black seed)
  • Mozaffari, F. S. et al (2000) — chemistry profile (Iranian steam-distilled)
  • Lawrence, B. M. (2008) — chemotype variation across countries (microwave-distilled)
  • El-Rab, M. O. G. & Al-Sheikh, O. A. (1995) — 2 dermatitis cases Saudi Arabia
  • Zedlitz, S. et al (2002) — ACD case report (eczema patient)
  • Steinmann, A. et al (1997) — ACD case report (28-y-old man)
  • Nosbaum, A. et al (2011) — erythema multiforme (oral capsules — fixed oil)
  • Gelot, P. et al (2012) — bullous eruption (oral + dermal)
  • Aqel, M. & Shaheen, R. (1996) — uterine smooth muscle spontaneous contraction inhibition
  • Yi, T. et al (2008) — antiangiogenic action of thymoquinone
  • Salim, E. I. & Fukushima, S. (2003) — DMH-colon antiproliferative
  • Ait M'barek, L. et al (2007a) — antitumor mouse models
  • Islam, S. N. et al (2004) — immunotoxicity rats + cytotoxicity stomach cell lines
  • Sultan, M. T. et al (2009) — subchronic toxicity 8-week dietary
  • Turkdogan, M. K. et al (2003) — hepatoprotective
  • Burits, M. & Bucar, F. (2000) — antioxidant
  • Hosseinzadeh, H. et al (2007) — lipid peroxidation protection
  • Abdel-Wahhab, M. A. & Aly, S. E. (2005) — aflatoxin protection
  • Al-Hader, A. et al (1993) — hypoglycemic effect rabbits
  • Kapur, R. (1948) — uterine herb survey post-childbirth
  • Badary, O. A. et al (1998) — thymoquinone oral LD50 mice
  • Jenner, P. M. et al (1964) — p-cymene oral LD50 rats