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MilliporeSigma

V9130

N-Vanillylnonanamide

≥97%, nicotinamide adenine dinucleotide phosphate inhibitor, powder

Synonym(s):

Capsaicin synthetic, N-(4-Hydroxy-3-methoxybenzyl)nonanamide, N-Vanillylpelargonamide, Nonanoic acid vanillylamide, Nonylvanylamide, Pelargonic acid vanillylamide, Pseudocapsaicin

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$75.20

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$210.00

$75.20


Estimated to ship onFebruary 24, 2026Details


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About This Item

Empirical Formula (Hill Notation):
C17H27NO3
CAS Number:
Molecular Weight:
293.40
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
219-484-1
MDL number:
Beilstein/REAXYS Number:
2144300
Assay:
≥97%
Form:
powder
Quality level:

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Product Name

N-Vanillylnonanamide, ≥97%, powder

form

powder

InChI

1S/C17H27NO3/c1-3-4-5-6-7-8-9-17(20)18-13-14-10-11-15(19)16(12-14)21-2/h10-12,19H,3-9,13H2,1-2H3,(H,18,20)

InChI key

RGOVYLWUIBMPGK-UHFFFAOYSA-N

SMILES string

CCCCCCCCC(=O)NCc1ccc(O)c(OC)c1

assay

≥97%

color

white to off-white

solubility

methanol: 100 mg/mL, clear to slightly hazy, colorless to deep brown-yellow

storage temp.

2-8°C

Quality Level

Gene Information

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This Item
15971PHL89820SML2637
form

powder

form

-

form

solid

form

powder

assay

≥97%

assay

≥98.0% (HPLC)

assay

≥95.0% (HPLC)

assay

≥98% (HPLC)

Quality Level

200

Quality Level

100

Quality Level

-

Quality Level

-

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

solubility

methanol: 100 mg/mL, clear to slightly hazy, colorless to deep brown-yellow

solubility

-

solubility

-

solubility

DMSO: 2 mg/mL, clear

color

white to off-white

color

-

color

-

color

white to beige

Application

N-Vanillylnonanamide has been used for the preparation of spicules.[1] It has also been used to reduce the firing of most extrinsic sensory axons.[2]

General description

N-Vanillylnonanamide has antifouling properties.[3] It acts as an nicotinamide adenine dinucleotide phosphate (NADPH) inhibitor.[4]

Other Notes

Synthetic analogue of capsaicin with similar bioactivity.

signalword

Danger

Hazard Classifications

Eye Dam. 1 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Coping with Biological Growth on Stone Heritage Objects: Methods, Products, Applications, and Perspectives (2017)
Measurement of strains experienced by viscerofugal nerve cell bodies during mechanosensitive firing using digital image correlation
Palmer G, et al.
American Journal of Physiology. Heart and Circulatory Physiology (2016)
Sphingolipids in Disease (2013)
R W Foster et al.
Pain, 25(2), 269-278 (1986-05-01)
The chemical irritants o-chlorobenzylidene malononitrile (CS), n-nonanoylvanillylamine (VAN) and dibenzoxazepine (CR) and several of its derivatives have been assayed using the human blister base. The relative potencies found by this method, CR greater than VAN greater than CS, conflicted with
Federica Villa et al.
Biotechnology letters, 31(9), 1407-1413 (2009-06-03)
The potential on N-vanillylnonanamide (NVN) in preventing the attachment of Pseudomonas stutzeri and a Bacillus cereus-group strain was investigated. NVN up to 852 microM was not toxic, nor was it an energy source for either organism. Microbial attachment assays were

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