ChemicalBook >> CAS DataBase List >>Piperine

Piperine

CAS No.
94-62-2
Chemical Name:
Piperine
Synonyms
Bioperine;(2E,4E)-5-(benzo[d][1,3]dioxol-5-yl)-1-(piperidin-1-yl)penta-2,4-dien-1-one;Piperin;FEMA 2909;Piperine Powder;1-PIPERYLPIPERIDINE;1-PIPEROYLPIPERIDINE;(E,E)-1-[5-(1,3-Benzodioxol-5-yl)-1-oxo-2,4-pentadienyl]-piperidine;PIPERINE;Piperine
CBNumber:
CB1249813
Molecular Formula:
C17H19NO3
Lewis structure
c17h19no3 lewis structure
Molecular Weight:
285.34
MDL Number:
MFCD00005839
MOL File:
94-62-2.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-27 23:15:50
Product description Number Pack Size Price
Piperine ≥95%, FG W290904 1 each $76.6
Piperine European Pharmacopoeia (EP) Reference Standard Y0001217 30 mg $167
Piperine ≥95%, FG W290904 100g $279
Piperine ≥95%, FG W290904 1kg $1590
Piperine Pharmaceutical Secondary Standard; Certified Reference Material PHR2211 50mg $182
More product size

Piperine Properties

Melting point 131-135 °C(lit.)
Boiling point 427.77°C (rough estimate)
Density 1.0864 (rough estimate)
refractive index 1.5400 (estimate)
FEMA 2909 | PIPERINE
FLAVIS Number 14.003 | Piperine
storage temp. Sealed in dry,Room Temperature
solubility Slightly soluble in water, 10% soluble in alcohol, soluble only in certain oils
form Crystalline Powder
pka 12.22(at 18℃)
color Off-white to tan or yellow-tan
Odor at 1.00 % in propylene glycol. pepper animal
Odor Type spicy
Water Solubility 40 mg/L (18 ºC)
JECFA Number 1600
Merck 14,7472
BRN 90741
Stability Stable. Incompatible with strong oxidizing agents.
Cosmetics Ingredients Functions SKIN CONDITIONING - MISCELLANEOUS
InChI 1S/C17H19NO3/c19-17(18-10-4-1-5-11-18)7-3-2-6-14-8-9-15-16(12-14)21-13-20-15/h2-3,6-9,12H,1,4-5,10-11,13H2/b6-2+,7-3+
InChIKey MXXWOMGUGJBKIW-YPCIICBESA-N
SMILES O=C(\C=C\C=C\c1ccc2OCOc2c1)N3CCCCC3
LogP 2.66
CAS DataBase Reference 94-62-2(CAS DataBase Reference)
Substances Added to Food (formerly EAFUS) PIPERINE
EWG's Food Scores 1
FDA UNII U71XL721QK
NCI Drug Dictionary Bioperine
NIST Chemistry Reference Piperine(94-62-2)
EPA Substance Registry System 2,4-Pentadien-1-one, 5-(1,3-benzodioxol-5-yl)-1-(1-piperidinyl)-, (2E,4E)- (94-62-2)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)Environment (GHS09)
GHS07,GHS09
Signal word  Warning
Hazard statements  H302-H411
Precautionary statements  P264-P270-P273-P301+P312-P391-P501
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xn,Xi,N
Risk Statements  22-21/22-20/21/22-51/53
Safety Statements  22-24/25-36/37-36-61
RIDADR  UN 3077 9 / PGIII
WGK Germany  3
RTECS  TN2321500
Hazard Note  Irritant
TSCA  TSCA listed
HS Code  29399990
Storage Class 11 - Combustible Solids
Hazard Classifications Acute Tox. 4 Oral
Aquatic Chronic 2
Toxicity LD50 orally in Rabbit: 514 mg/kg
NFPA 704
0
1 0

Piperine price More Price(131)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich W290904 Piperine ≥95%, FG 94-62-2 1 each $76.6 2026-04-30 Buy
Sigma-Aldrich Y0001217 Piperine European Pharmacopoeia (EP) Reference Standard 94-62-2 30 mg $167 2026-04-30 Buy
Sigma-Aldrich W290904 Piperine ≥95%, FG 94-62-2 100g $279 2026-04-30 Buy
Sigma-Aldrich W290904 Piperine ≥95%, FG 94-62-2 1kg $1590 2026-04-30 Buy
Sigma-Aldrich PHR2211 Piperine Pharmaceutical Secondary Standard; Certified Reference Material 94-62-2 50mg $182 2026-04-30 Buy
Product number Packaging Price Buy
W290904 1 each $76.6 Buy
Y0001217 30 mg $167 Buy
W290904 100g $279 Buy
W290904 1kg $1590 Buy
PHR2211 50mg $182 Buy

Piperine Chemical Properties,Uses,Production

Description

Piperine is an alkaloid responsible for the taste and fl avor of pepper. In pure form it exists as a yellow to pale-yellow crystal, with a burning taste and pungent order. It is found naturally in plants in the Piperaceae family, particularly Piper nigrum (black pepper) and Piper longum (Indian long pepper). Piper nigrum is a perennial woody vine that grows to approximately 30 feet. It produces spikelike flowers that hold berries called peppercorns.

Chemical Properties

Piperine is odorless. It is tasteless at first, but develops a burning aftertaste of pepper.

Chemical Properties

light yellow powder

Occurrence

Reported found in black pepper; also in Piper longum, Piper officinarum, Piper lowong BI., Piper famechoni, Piper chaba and the leaves of Rhododendron fauriae var. rupescens.

History

Hans Christian Oersted (1777 1851) isolated piperine from black pepper in 1819 and published his findings in 1820. Oersted extracted a resin from pepper plants with alcohol, formed a soluble saltby adding hydrochloric acid with alcohol, and then separated piperine from solution by precipitation and distillation. In 1882, Leopold Rügheimer (1850 1917) synthesized piperine from piperinic acid chloride and piperidine. The complete synthesis of piperine was reported in 1894 by Albert Ladenburg (1842 1911) and M. Scholtz. Ladenburg and Scholtz used piperonal (C8H6O3) and acetaldehyde (CH3CHO) to produce piperinic acid (C12H10O4), which was then reacted with thionyl chloride (COCl2) and piperidine (C5H11N) to produce piperine.

Uses

Piperine is used in granular formulations as a pesticide against small animals such as dogs, cats, skunks, raccoons, and squirrels. Piperine pesticides are nontoxic and operate as a repellant when animals smell or test them. Piperine is also incorporated with other compounds to make insecticides; it is effective against houseflies, lice, and various other pests.
Piperine has been used medicinally for thousands of years and this continues today. It is used to treat asthma and chronic bronchitis. It also has putative analgesic and antiinfl ammatory properties that stem from its antioxidant properties. Research is examining the use of piperine in treating malaria. Antiepilepsirine is a derivative of piperine that is used to treat different types of epilepsy, especially in China. A current area of interest is the efficacy of piperine in increasing the bioavailability of certain nutrients and drugs. It is thought to possibly aid digestion and increase the absorption in the digestive tract of numerous drugs used as cancer treatments, antihistamines, steroidal inflammation reducers, and antibiotics.

Uses

The alkaloid which gives pepper its spiciness, and has been used as an organic insecticide.

Uses

analeptic, antibacterial

Uses

A black pepper extract TRPV1 activator.
It finds use in flavor compositions, not only as ingredient in artificial Black Pepper, but also in various spice blends, and as an additive to the flavor composition used in "Celery Soda" (a carbonated beverage of sweet, but pungent Celery flavor, sometimes used as an appetizer).

Preparation

From piperoyl chloride and piperidine.

Definition

ChEBI: Piperine is a N-acylpiperidine that is piperidine substituted by a (1E,3E)-1-(1,3-benzodioxol-5-yl)-5-oxopenta-1,3-dien-5-yl group at the nitrogen atom. It is an alkaloid isolated from the plant Piper nigrum. It has a role as a NF-kappaB inhibitor, a plant metabolite, a food component and a human blood serum metabolite. It is a member of benzodioxoles, a N-acylpiperidine, a piperidine alkaloid and a tertiary carboxamide. It is functionally related to an (E,E)-piperic acid.

Safety Profile

Poison by ingestion and intraperitoneal routes. An experimental teratogen. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of NOx.

Purification Methods

Piperine crystallises as light yellow crystals from EtOH or EtOAc (m 132o), aqueous EtOH (m 128-129o), Et2O (m129o), or*benzene/ligroin. [Beilstein 20 H 79, 20 I 23, 20 II 53, 20 III/IV 1341, 20/3 V 469.]

References

Oersred., Schweigger's Journal, 29, 80 (1819)
Fliickiger, Hanbury., Pharmacographica, 584 London (1879)
Stenhouse., Pharm. J., 14,363 (1855)
Cazeneuve, Caillot., Bull. Soc. Chim. Fr., 27,291 (1877)
Riigheimer., Ber., 15, 1391 (1882)
Peinemann., Arch. Pharm., 234, 245 (1896)
Newman., Chem. Products, 16,379 (1953)

110-89-4
136-72-1
94-62-2
Synthesis of Piperine from Piperidine and 5-(3,4-METHYLENEDIOXYPHENYL)-2,4-PENTADIENOIC ACID

Piperine Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 549)Suppliers
Supplier Tel Email Country ProdList Advantage
PNP Biotech Co. Ltd
+8618516098983 sales@pnpbiotech.com China 1001 58
Nantong Guangyuan Chemicl Co,Ltd
+undefined17712220823 admin@guyunchem.com China 615 58
Hebei Zhuanglai Chemical Trading Co.,Ltd
+8613343047651 admin@zlchemi.com China 3692 58
Shaanxi Xianhe Biotech Co., Ltd
+86-17709210191; +8617709210191 Jerry@xhobio.com China 906 58
Lianyungang Kaiyu Environmental Tech Co., Ltd.
+86-0086-19851820538 +8619851820538 carlos@khonorchem.com China 314 58
Hefei Lbao Physical & Chemical Science Co.,Ltd
+15184799099 lbaochemicals@gmail.com China 670 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806 sales@capot.com China 29640 60
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21587 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
Shanghai Zheyan Biotech Co., Ltd.
18017610038 zheyansh@163.com CHINA 3619 58

View Lastest Price from Piperine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Piperine pictures 2026-06-06 Piperine
94-62-2
0.99 RongNa Biotechnology Co.,Ltd
Piperine; Sichuan?Pepper oil pictures 2026-06-06 Piperine; Sichuan?Pepper oil
1KG >99% HPLC 1000KG Changsha Staherb Natural Ingredients Co., Ltd.
Piperine pictures 2026-06-02 Piperine
94-62-2
1kg 0.99 1000kg Shaanxi Xianhe Biotech Co., Ltd
  • Piperine pictures
  • Piperine
    94-62-2
  • 0.99
  • RongNa Biotechnology Co.,Ltd
  • Piperine pictures
  • Piperine
    94-62-2
  • $0.00
  • 0.99
  • Shaanxi Xianhe Biotech Co., Ltd
(E,E)-1-[5-(1,3-Benzodioxol-5-yl)-1-oxo-2,4-pentadienyl]-piperidine 5-BENZO[1,3]DIOXOL-5-YL-1-PIPERIDIN-1-YL-PENTA-2,4-DIEN-1-ONE PIPERINE N-PIPEROYLPIPERIDIN 1-PIPERONYLPIPERIDINE 1-PIPEROYLPIPERIDINE 1-PIPERYLPIPERIDINE 1-[5-(1,3-BENZODIOXOL-5-YL)-2,4-PENTADIENOYL]PIPERIDINE 1-(5-(1,3-benzodioxol-5-yl)-1-oxo-2,4-pentadienyl)-,(e,e)-piperidin 1,3-Benzodioxol-5-yl-1-oxo-2,4-pentadienyl-piperidine 5-(1,3-BENZODIOXOL-5-YL)-1-OXO-2E,4E-PENTADIENYL-PIPERD. PIPERIDINE,1-PIPERONYL- Natural piperine (1-piperidinyl)-,(2E, 4E)- 2,4-Pentadien-1-one,5-(1,3-benzodioxol-5-yl)-1- (E,E)-1-[5-(1,3-Benzodioxol-5-yl)-2,4-pentadienoyl]piperidine (E,E)-5-(3,4-Methylenedioxyphenyl)-2,4-pentadienoylpiperidide 2,4-Pentadien-1-one, 5-(1,3-benzodioxol-5-yl)-1-(1-piperidinyl)-, (2E,4E)- (2E,4E)-1-(1-Piperidinyl)-5-(1,3-benzodioxole-5-yl)-2,4-pentadiene-1-one 1-[(2E,4E)-5-(1,3-Benzodioxol-5-yl)-1-oxo-2,4-pentadienyl]piperidine Piperine,99% (E,E)-1-Piperoylpiperidine Piperylpiperidine Piperine(1-Piperoylpiperidine) (2E,4E)-5-(1,3-Benzodioxol-5-yl)-1-(1-piperidinyl)-2,4-pentadien-1-one NSC 21727 1-[5-(1,3-Benzodioxol-5-yl)-2,4-pentadienoyl]piperidine 1-Piperoylpiperidine 1-Piperylpiperidine 1,3-benzodioxol-5-yl-1-oxo-2,4-pentadienyl-piperine 1-[(2E,4E)-5-(1,3-Benzodioxol-5-yl)-2,4-pentadienoyl]piperidine 1-[5-(1,3-benzodioxol-5-yl)-1-oxo-2,4-pentadienyl]-,(e,e)-piperidin 1-[5-(1,3-benzodioxol-5-yl)-1-oxo-2,4-pentadienyl]-,(E,E)-Piperidine 1-piperoyl-,(e,e)-piperidin 1-trans,trans-piperinoyl-piperidine Piperidine, 1-[5-(1,3-benzodioxol-5-yl)-1-oxo-2,4-pentadienyl]-, (E,E)- Piperidine, 1-piperoyl-, (E,E)- PIPERINE 97+% Piperine,98% Piperidine, 1-(2E,4E)-5-(1,3-benzodioxol-5-yl)-1-oxo-2,4-pentadienyl- 1-piperinoylpiperidine PIPERINE(P) PIPERINE(RG) PIPERLINE Piperine SynonyMs (E,E)-1-[5-(1,3-Benzodioxol-5-yl)-1-oxo-2,4-pentadienyl]-piperidine Piperine (E,E)-1-[5-(1,3-Benzodioxol-5-yl)-1-oxo-2,4-pentadienyl]-piperidine Hot sale Piperine 90%min CAS NO.94-62-2 Piperine 94-62-2 Piperine> Piperine CRS Piperine USP/EP/BP Black Pepper Extract 95% Piperine (E,E)-piperine Piperin-d10Q: What is Piperin-d10 Q: What is the CAS Number of Piperin-d10 Piperine (Y0001217) PiperineQ: What is Piperine Q: What is the CAS Number of Piperine Q: What is the storage condition of Piperine (2E,4E)-5-(1,3-benzodioxol-5-yl)-1-piperidin-1-ylpenta-2,4-dien-1-one Piperine (1543200) Autophagy,Piperine,Endogenous Metabolite,Cluster of differentiation 243,Inhibitor,Multidrug resistance protein 1,CD243,ABCB1,P-gp,P-glycoprotein,inhibit,Pgp,MDR1 Piperine, 98% (Custom work)