Dihydrocapsaicin

  • CasNo:19408-84-5
  • purity:99%
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Details

Factory Sells Best Quality Dihydrocapsaicin 19408-84-5 with USP

  • Molecular Formula: C18H29NO3
  • Molecular Weight: 307.433
  • Appearance/Colour: White to off-white solid 
  • Vapor Pressure: 1.61E-10mmHg at 25°C 
  • Melting Point: 62-65 °C(lit.) 
  • Refractive Index: 1.51 
  • Boiling Point: 497.4 °C at 760 mmHg 
  • PKA: 9.76±0.20(Predicted) 
  • Flash Point: 254.6 °C 
  • PSA: 58.56000 
  • Density: 1.026 g/cm3 
  • LogP: 4.40450 

Dihydrocapsaicin(Cas 19408-84-5) Usage

Biochem/physiol Actions

VR1 vanilloid receptor agonist.

General Description

Dihydrocapsaicin belongs to the capsaicinoid group of compounds which are responsible for the pungency of capsicum fruits.

InChI:InChI=1/C18H29NO3/c1-14(2)8-6-4-5-7-9-18(21)19-13-15-10-11-16(20)17(12-15)22-3/h10-12,14,20H,4-9,13H2,1-3H3,(H,19,21)

19408-84-5 Relevant articles

Preparation method of capsaicin and capsaicin prepared by using method

-

Paragraph 0037; 0127-0140, (2021/06/26)

The invention relates to a capsaicin pre...

Preparation method of capsaicine and capsaicine prepared by method

-

Paragraph 0124-0128, (2021/04/07)

The invention provides a preparation met...

Regioselective hydroxylation and dehydrogenation of capsaicin and dihydrocapsaicin by cultured cells of Phytolacca americana

Hamada, Hiroki,Ono, Tsubasa,Shimoda, Kei

, p. 103 - 107 (2022/03/18)

The biotransformations of capsaicin and ...

Vanilla amide synthesis method

-

Paragraph 0049-0052; 0074-0076, (2021/06/13)

The invention discloses a vanilla amide ...

19408-84-5 Process route

Vanillylamin
1196-92-5

Vanillylamin

8-methylnonanoic acid
5963-14-4

8-methylnonanoic acid

dihydrocapsaicin
19408-84-5

dihydrocapsaicin

Conditions
Conditions Yield
With triethyl borate; In toluene; for 4h; Reagent/catalyst; Dean-Stark; Reflux; Green chemistry;
88%
In ethanol; at 50 ℃;
83%
With SiO2-H3BO3; In toluene; for 6h; Reflux;
82%
With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In octane; at 90 ℃; for 15h; Temperature; Reagent/catalyst; Solvent; Inert atmosphere;
1-iodo-7-methyloctane
10266-06-5

1-iodo-7-methyloctane

carbon monoxide
201230-82-2

carbon monoxide

vanillylamine hydrochloride
7149-10-2

vanillylamine hydrochloride

dihydrocapsaicin
19408-84-5

dihydrocapsaicin

Conditions
Conditions Yield
1-iodo-7-methyloctane; carbon monoxide; vanillylamine hydrochloride; With potassium carbonate; 1,1,1,3,3,3-hexamethyl-disilazane; tetrakis(triphenylphosphine) palladium(0); In benzene; for 16h; under 34200 Torr; Photolysis;
With tetrabutyl ammonium fluoride; In tetrahydrofuran; chloroform; at 20 ℃; for 3h;
82%

19408-84-5 Upstream products

  • 1196-92-5
    1196-92-5

    Vanillylamin

  • 205651-88-3
    205651-88-3

    8-methyl-nonanoyl chloride

  • 404-86-4
    404-86-4

    capsaicin

  • 25775-90-0
    25775-90-0

    cis-capsaicin

19408-84-5 Downstream products

  • 103906-29-2
    103906-29-2

    8-methylnonanamide

  • 2555-98-8
    2555-98-8

    3-(4-formyl-2-methoxyphenoxy)-4-hydroxy-5-methoxybenzaldehyde

  • 121-33-5
    121-33-5

    vanillin

  • 1224428-95-8
    1224428-95-8

    2-(4-isobutyl-phenyl)-propionic acid 2-methoxy-4-[(8-methylnonanoylamino)-methyl]-phenyl ester

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