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Safety Information

SMB00093

Sigma-Aldrich

Pipernonaline

≥95% (LC/MS-ELSD)

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About This Item

Empirical Formula (Hill Notation):
C21H27NO3
CAS Number:
88660-10-0
Molecular Weight:
341.44
MDL number:
MFCD24849304
UNSPSC Code:
12352205
PubChem Substance ID:
329824771
NACRES:
NA.25

Assay

≥95% (LC/MS-ELSD)

form

solid

application(s)

metabolomics
vitamins, nutraceuticals, and natural products

storage temp.

−20°C

SMILES string

O=C(\C=C\CCCC\C=C\c1ccc2OCOc2c1)N3CCCCC3

InChI

1S/C21H27NO3/c23-21(22-14-8-5-9-15-22)11-7-4-2-1-3-6-10-18-12-13-19-20(16-18)25-17-24-19/h6-7,10-13,16H,1-5,8-9,14-15,17H2/b10-6+,11-7+

InChI key

PKLGRWSJBLGIBF-JMQWPVDRSA-N

General description

Natural product derived from plant source.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H413

Precautionary Statements

P273 - P301 + P312 + P330

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 4

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

SMB00093-1MG:

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Certificates of Analysis (COA)

Lot/Batch Number
122228319V
12222877V
122228-77V

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Zhuang Jin et al.
Phytotherapy research : PTR, 23(8), 1194-1196 (2009-01-28)
A bioassay-guided isolation of an ethanol extract of the fruit of Piper longum L. yielded piperlonguminine, piperine and pipernonaline, as the main antihyperlipidemic constituents. They exhibit appreciable antihyperlipidemic activity in vivo, which is comparable to that of the commercial antihyperlipidemic
Seung Woong Lee et al.
Bioorganic & medicinal chemistry letters, 18(16), 4544-4546 (2008-08-02)
Eight alkamides 1-8 were isolated by bioassay-guided isolation of EtOH extracts of the fruits of Piper longum and Piper nigum (Piperaceae). Their structures were elucidated by spectroscopic analysis ((1)H, (13)C NMR, and ESI-MS) as follows: guineensine (1), retrofracamide C (2)

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