Basic information Description References Safety Supplier Related
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Nonivamide

Basic information Description References Safety Supplier Related

Nonivamide Basic information

Product Name:
Nonivamide
Synonyms:
  • Nonivamide(Synthetic Capsaicin)
  • N-((Hydroxy-3-methoxyphenyl)methyl)4-nonanamide
  • N-Nonanoyl vanillylamide
  • Nonanamide, N-((4-hydroxy-3-methoxyphenyl)meth
  • SYNTHETIC CAPSAICIN
  • PELARGONYL VANILLYLAMIDE
  • PELARGONIC ACID VANILLYLAMIDE
  • N-PELARGONIC ACID VANILLYLAMIDE
CAS:
2444-46-4
MF:
C17H27NO3
MW:
293.4
EINECS:
219-484-1
Product Categories:
  • Anilines, Aromatic Amines and Nitro Compounds
  • INORGANIC & ORGANIC CHEMICALS
  • Plant extract
  • Herb extract
  • Inhibitors
  • API
  • 2444-46-4
Mol File:
2444-46-4.mol
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Nonivamide Chemical Properties

Melting point:
54°C
Boiling point:
200-210 °C(Press: 0.05 Torr)
Density 
1,1 g/cm3
FEMA 
2787 | NONANOYL 4-HYDROXY-3-METHOXYBENZYLAMIDE
Flash point:
190°C
storage temp. 
Sealed in dry,2-8°C
solubility 
methanol: 100 mg/mL, clear to slightly hazy
form 
powder
pka
9.76±0.20(Predicted)
color 
white to off-white
Odor
bland odorless
Odor Type
bland
JECFA Number
1599
BRN 
2144300
Stability:
Stable. Incompatible with strong oxidizing agents.
InChIKey
RGOVYLWUIBMPGK-UHFFFAOYSA-N
LogP
3.43
CAS DataBase Reference
2444-46-4(CAS DataBase Reference)
EPA Substance Registry System
Nonanamide, N-[(4-hydroxy-3-methoxyphenyl)methyl]- (2444-46-4)
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Safety Information

Hazard Codes 
T,Xi
Risk Statements 
25-36/37/38-43
Safety Statements 
26-45-37/39-36/37
RIDADR 
UN 3462 6.1/PG 2
WGK Germany 
3
RTECS 
RA5998000
19
HazardClass 
6.1
PackingGroup 
II
HS Code 
29242990
Toxicity
mouse,LD50,intraperitoneal,8mg/kg (8mg/kg),Journal of Medicinal Chemistry. Vol. 36, Pg. 2595, 1993.

MSDS

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Nonivamide Usage And Synthesis

Description

Nonivamide is also called pelargonic acid vanillylamide or PAVA. It is a capsaicinoid. Nonivamide, isolated from peppers, is a naturally occurring analog of capsaicin (sc-3577). Similar to capsaicin, nonivamide can activate the TRPV1 receptor, thus, stimulate the firing rate of dopaminergic neurons in the ventral tegmental area of the brain and to increase the expression of the serotonin receptor gene HTR2A. Nonivamide is with lower TRPV1 binding affinity, thus, a reduced pungency (9 200 000 scoville heat units) compared to capsaicin (16 000 000 scoville heat units).
Nonivamide is used in the food production to add a hot sensation to flavoring agents and spice mixtures. It is also used in the sweets and confectionary industries to add hot sensation into products. In pharmaceutical industries, nonivamide is used as a cheaper alternative for capsaicin. Warming or heating ointment of nonivamide is used for temporary relief of pain from conditions such as rheumatism, arthritis, lumbao, muscular aches, sprains and strains, sporting injuries and other conditions where local warmth is beneficial. Finalgon is one of the common product utilizing nonivamide for this purpose. Nonivamide is also used as an incapacitant spray, affecting the assailed person’s eyes, causing intense pain and swelling.

References

[1] https://www.scbt.com/scbt/product/nonivamide-2444-46-4
[2] https://pubchem.ncbi.nlm.nih.gov/compound/N-Vanillylnonanamide#section=Clinical-Trials
[3] https://cot.food.gov.uk/sites/default/files/cot/cotsection.pdf

Description

Nonanoyl-4-hydroxy-3-methoxybenzylamide is odorless with a pungent, burning taste. Synthesized from nonanyl chloride and vanillylamine.

Chemical Properties

n-Nonanyl-4-hydroxy-3-methoxybenzyl-amide is an odorless compound, but has a pungent, burning taste

Chemical Properties

solid

Uses

analgesic (topical), depletes Substance P

Uses

N-Vanillylnonanamide is a synthetic analogue of Capsaicin (175680) with similar bioactivity.

Definition

ChEBI: A capsaicinoid that is the carboxamide resulting from the formal condensation of the amino group of 4-hydroxy-3-methoxybenzylamine with the carboxy group of nonanoic acid. It is the active ingredient in many pepper sprays.

Preparation

From nonanyl chloride and vanillylamine.

References

1. m. j. caterina, m. a. schumacher, m. tominaga, t. a. rosen, j. d. levine and d. julius, nature 1997, 389, 816-824. 2. y. g. gil and m. k. kang, life sci 2008, 82, 997-1003. 3. y. s. lee, d. h. nam and j. a. kim, cancer lett 2000, 161, 121-130. 4. h. c. chang, s. t. chen, s. y. chien, s. j. kuo, h. t. tsai and d. r. chen, hum exp toxicol 2011, 30, 1657-1665. 5. k. c. brown, t. r. witte, w. e. hardman, h. luo, y. c. chen, a. b. carpenter, j. k. lau and p. dasgupta, plos one 2010, 5, e10243.>

Nonivamide Preparation Products And Raw materials

Preparation Products

NonivamideSupplier

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