Nordihydrocapsaicin

Nordihydrocapsaicin
Nordihydrocapsaicin
Heat	Above peak; (pure Nordihydrocapsaicin is highly toxic)
Scoville scale	9,100,000 SHU

Nordihydrocapsaicin
Names
	Preferred IUPAC name N-[(4-Hydroxy-3-methoxyphenyl)methyl]-7-methyloctanamide
	Other names N-Vanillyl-7-methyloctanamide; Vanillylamide of 7-methyloctanoic acid; NDHC
Identifiers
CAS Number	28789-35-7 ;
3D model (JSmol)	Interactive image;
ChemSpider	147689 ;
ECHA InfoCard	100.208.673
PubChem CID	168836;
UNII	RF657P8DA8 ;
CompTox Dashboard (EPA)	DTXSID3042217 ;
	InChI InChI=1S/C17H27NO3/c1-13(2)7-5-4-6-8-17(20)18-12-14-9-10-15(19)16(11-14)21-3/h9-11,13,19H,4-8,12H2,1-3H3,(H,18,20) Key: VQEONGKQWIFHMN-UHFFFAOYSA-N ; InChI=1/C17H27NO3/c1-13(2)7-5-4-6-8-17(20)18-12-14-9-10-15(19)16(11-14)21-3/h9-11,13,19H,4-8,12H2,1-3H3,(H,18,20) Key: VQEONGKQWIFHMN-UHFFFAOYAS;
	SMILES CC(C)CCCCCC(=O)NCC1=CC(=C(C=C1)O)OC;
Properties
Chemical formula	C17H27NO3
Molar mass	293.407 g·mol−1
Solubility in water	Negligible
Solubility	Soluble in DMSO, chloroform
Hazards
	GHS labelling:
Pictograms
Hazard statements	H300, H315, H319, H335
Precautionary statements	P264, P270, P280, P302+P352, P305+P351+P338, P321, P330, P362+P364, P405, P501
NFPA 704 (fire diamond)	4 0 0
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Nordihydrocapsaicin is a capsaicinoid and analog and congener of capsaicin in chili peppers (Capsicum).

Properties[edit]

Like capsaicin, it is an irritant. Nordihydrocapsaicin accounts for about 7% of the total capsaicinoids mixture^[2] and has about half the pungency of capsaicin. Pure nordihydrocapsaicin is a lipophilic colorless odorless crystalline to waxy solid. On the Scoville scale it has 9,100,000 SHU (Scoville heat units),^[1] significantly higher than pepper spray.

References[edit]

^ ^a ^b Govindarajan, Sathyanarayana (1991). "Capsicum — Production, Technology, Chemistry, and Quality. Part V. Impact on Physiology, Pharmacology, Nutrition, and Metabolism; Structure, Pungency, Pain, and Desensitization Sequences". Critical Reviews in Food Science and Nutrition. 29 (6): 435–474. doi:10.1080/10408399109527536. PMID 2039598.
^ Bennett DJ, Kirby GW (1968). "Constitution and biosynthesis of capsaicin". J. Chem. Soc. C: 442. doi:10.1039/j39680000442.

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[Govindarajan_Sathyanarayana_1991-1] Govindarajan, Sathyanarayana (1991). "Capsicum — Production, Technology, Chemistry, and Quality. Part V. Impact on Physiology, Pharmacology, Nutrition, and Metabolism; Structure, Pungency, Pain, and Desensitization Sequences". Critical Reviews in Food Science and Nutrition. 29 (6): 435–474. doi:10.1080/10408399109527536. PMID 2039598.

[2] Bennett DJ, Kirby GW (1968). "Constitution and biosynthesis of capsaicin". J. Chem. Soc. C: 442. doi:10.1039/j39680000442.

[1]

[2]

Properties[edit]

See also[edit]

References[edit]