Black Haw

Botanical Overview

Black Haw (Viburnum prunifolium) belongs to the Caprifoliaceae family. While not among the most extensively documented medicinal plants, this species has recorded uses that warrant attention from researchers and practitioners. This species belongs to the Caprifoliaceae family, a group of flowering plants.

General Description

Viburnum prunifolium (known as blackhaw or black haw, blackhaw viburnum, sweet haw, and stag bush) is a species of Viburnum native to eastern North America, from Connecticut west to eastern Kansas, and south to Alabama and Texas.

ⓘ Information
Description adapted from Wikipedia (CC BY-SA 4.0).

Family Context

The Caprifoliaceae family is widely distributed. Notable medicinal members include:

Geographic Distribution

Black Haw has been recorded in 10 countries and territories worldwide, including Austria, Belgium, Canada, China, Germany, and others.

Traditional Uses

Black Haw has been traditionally used for respiratory conditions, urinary tract health, and nervous system disorders, among other applications.

Respiratory conditions.

  • Asthma

Respiratory conditions are addressed through steam inhalation of the herb’s vapors or internal use as a warm tea. The hot infusion acts as an expectorant, helping to loosen phlegm and clear congestion. Some traditions combine it with honey for coughs.

Urinary tract health.

  • Diuretic

Urinary tract applications typically involve drinking the herb as a mild tea, which increases urine production and helps flush the urinary system. It may be combined with other demulcent herbs to soothe irritated tissues.

Nervous system disorders.

  • Nervine
  • Sedative
  • Spasm

Nervous system support involves taking the herb as a warm tea, often in the evening or before bed. The calming compounds interact with neurotransmitter systems to promote relaxation and restful sleep.

Active Compounds

Phytochemical research has identified 30 compounds in this species, including a diverse array of phytochemical classes (see the Complete Chemical Inventory below for the full list).

The identified compounds include the following categories:

  • Flavonoid: antioxidant compounds that protect cells from oxidative damage
  • Phenolic: antioxidant compounds that neutralize free radicals
  • Sterol: cholesterol-like compounds with anti-inflammatory properties
ⓘ Information
Information on this page is compiled from Dr. Duke’s Phytochemical and Ethnobotanical Databases (USDA ARS), a public domain resource. Consult a healthcare professional before using any herbal preparation.
⚠ Caution
Traditional records: This plant has documented uses including Abortifacient. Self-medication with herbs carries risks including allergic reactions, drug interactions, and toxicity. Only use under the supervision of a qualified healthcare professional.

Distribution and Conservation

Reported distribution: Austria, Belgium, Canada, China, Germany, France, Mexico, Poland, United States, Unknown.

Complete Use Records

CategoryCultural Context
DiureticElsewhere, US
NervineTurkey, US
SedativeElsewhere, Turkey
SpasmElsewhere, Turkey
AbortifacientUS
AstringentUS
MedicineUS(Appalachia)
TonicUS
UterosedativeUS
UterotonicTurkey
UteritisElsewhere
AsthmaTurkey

Complete Chemical Inventory

CompoundFormulaMW
1-METHYL-2,3-DIBUTYL-HEMIMELLITATE
ACETIC-ACIDC₂H₄O₂60.05 Da
ACETYL-OLEANOLIC-ACIDC₃₂H₅₀O₄498.7 Da
ACETYLURSOLIC-ACIDC₃₂H₅₀O₄498.7 Da
AESCULETINC₉H₆O₄178.14 Da
ALPHA-AMYRINC₃₀H₅₀O426.7 Da
AMENTOFLAVONEC₃₀H₁₈O₁₀538.5 Da
ARBUTINC₁₂H₁₆O₇272.25 Da
BETA-AMYRINC₃₀H₅₀O426.7 Da
BETA-SITOSTEROLC₂₉H₅₀O414.7 Da
CAPRONIC-ACIDC₆H₁₂O₂116.16 Da
CAPRYLIC-ACIDC₈H₁₆O₂144.21 Da
CHLOROGENIC-ACIDC₁₆H₁₈O₉354.31 Da
CITRIC-ACIDC₆H₈O₇192.12 Da
D-CATECHINC₁₅H₁₄O₆290.27 Da
DEXTRINC₁₈H₃₂O₁₆504.4 Da
ESCULETINC₉H₆O₄178.14 Da
FORMIC-ACIDCH₂O₂46.025 Da
GLUCOSEC₆H₁₂O₆180.16 Da
HEPTACOSANEC₂₇H₅₆380.7 Da
ISOCHLOROGENIC-ACIDC₁₆H₁₈O₉354.31 Da
ISOVALERIANIC-ACIDC₅H₁₀O₂102.13 Da
ISOVALERIC-ACIDC₅H₁₀O₂102.13 Da
LINOLEIC-ACIDC₁₈H₃₂O₂280.4 Da
MALIC-ACIDC₄H₆O₅134.09 Da
MYRISTIC-ACIDC₁₄H₂₈O₂228.37 Da
N-HEPTACOSANEC₂₇H₅₆380.7 Da
OLEANOLIC-ACIDC₃₀H₄₈O₃456.7 Da
OLEANOLIC-ACID-ACETATEC₃₂H₅₀O₄498.7 Da
OLEIC-ACIDC₁₈H₃₄O₂282.5 Da

Data from PubChem (NIH/NLM, public domain).


References & Further Reading

External Research Links

Data Sources