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ChemicalBook >> CAS DataBase List >>Vanillylidenacetone

Vanillylidenacetone

CAS No.
1080-12-2
Chemical Name:
Vanillylidenacetone
Synonyms
DEHYDROZINGERONE;feruloylmethane;VANILLYLIDINE ACETONE;4-(4-HYDROXY-3-METHOXYPHENYL)BUT-3-EN-2-ONE;4-(4-HYDROXY-3-METHOXYPHENYL)-3-BUTEN-2-ONE;mhsk;FEMA 3738;vanillalacetone;Dehydrogingerone;Vanillideneacetone
CBNumber:
CB2126546
Molecular Formula:
C11H12O3
Molecular Weight:
192.21
MDL Number:
MFCD00012210
MOL File:
1080-12-2.mol
MSDS File:
SDS
Last updated:2026-05-27 23:54:55
Product description Number Pack Size Price
Vanillylidenacetone ≥98.5% 07551 5G-F $102
Vanillylidenacetone ≥98.5% 07551 5G $102
Vanillylidenacetone analytical standard 90609 100mg $69.5
Vanillylideneacetone FV07091 50g $253.5
Vanillylideneacetone FV07091 100g $362
More product size

Vanillylidenacetone Properties

Melting point 125-130 °C
Boiling point 268.19°C (rough estimate)
Density 1.1503 (rough estimate)
refractive index 1.4600 (estimate)
FEMA 3738 | VANILLYLIDENE ACETONE
FLAVIS Number 07.046 | Vanillylidene acetone
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
solubility Soluble in DMSO (up to 25 mg/ml) or in Ethanol (up to 20 mg/ml).
form solid
pka 9.94±0.31(Predicted)
color Pale yellow
Odor at 100.00 %. sweet powdery vanilla creamy balsam
Odor Type vanilla
JECFA Number 732
Stability Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 1 month.
InChI 1S/C11H12O3/c1-8(12)3-4-9-5-6-10(13)11(7-9)14-2/h3-7,13H,1-2H3/b4-3+
InChIKey AFWKBSMFXWNGRE-ONEGZZNKSA-N
SMILES COc1cc(\C=C\C(C)=O)ccc1O
LogP 1.40
CAS DataBase Reference 1080-12-2(CAS DataBase Reference)
Substances Added to Food (formerly EAFUS) VANILLYLIDENE ACETONE
EWG's Food Scores 1
FDA UNII 8CJX5I27B7
EPA Substance Registry System 3-Buten-2-one, 4-(4-hydroxy-3-methoxyphenyl)- (1080-12-2)
UNSPSC Code 12352200
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
PPE Eyeshields, Gloves, type N95 (US)
Risk Statements  36/37/38
Safety Statements  26-36/37/39
WGK Germany  3
RTECS  EM9960000
10-23
TSCA  TSCA listed
HS Code  29145090
Storage Class 11 - Combustible Solids
Toxicity LD50 intraperitoneal in mouse: 610mg/kg

Vanillylidenacetone price More Price(51)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 07551 Vanillylidenacetone ≥98.5% 1080-12-2 5G-F $102 2023-06-20 Buy
Sigma-Aldrich 07551 Vanillylidenacetone ≥98.5% 1080-12-2 5G $102 2023-01-07 Buy
Sigma-Aldrich 90609 Vanillylidenacetone analytical standard 1080-12-2 100mg $69.5 2022-05-15 Buy
Biosynth FV07091 Vanillylideneacetone 1080-12-2 50g $253.5 2026-06-04 Buy
Biosynth FV07091 Vanillylideneacetone 1080-12-2 100g $362 2026-06-04 Buy
Product number Packaging Price Buy
07551 5G-F $102 Buy
07551 5G $102 Buy
90609 100mg $69.5 Buy
FV07091 50g $253.5 Buy
FV07091 100g $362 Buy

Vanillylidenacetone Chemical Properties,Uses,Production

Description

Dehydrozingerone (1080-12-2) is a structural half analog of curcumin (Cat.# 10-1243) and is isolated from ginger rhizomes. Dehydrozingerone displays antioxidant, antibacterial and antifungal properties.1 It has also been shown to possess various antitumor effects2,3 and inhibit growth factor/peroxide-stimulated vascular smooth muscle function4.

Chemical Properties

Vanillylidene acetone has a very sweet, warm and tenacious odor.

Physical properties

Yellowish, needlelike crystals. Slightly soluble in water, soluble in alcohol and oils.

Uses

Vanillylidenacetone is one of ferulic acid derivatives. Studies have shown that vanillyl acetone has a certain inhibitory effect on Amaranthus, barnyardgrass, matang, dogwood and rape, among which the best inhibitory effect is on rape and Amaranthus.

Definition

ChEBI: Dehydrozingerone is a hydroxycinnamic acid.

Taste threshold values

Taste characteristics at 200 ppm: balsamic vanilla, with sweet aromatic spicy nuances.

Synthesis

Vanillin

121-33-5

Acetone

67-64-1

Vanillylidenacetone

1080-12-2

General method: 20% (w/v) aqueous NaOH solution was slowly added to an ethanol solution of vanillin (6a1-d1,6e,6f) and acetone (10-25 eq., excess) at 0-5 °C. The reaction mixture was stirred at room temperature and the progress of the reaction was monitored by thin layer chromatography (TLC). When the vanillin was completely consumed, the excess acetone was evaporated under reduced pressure; subsequently, cold water was added and the resulting mixture was acidified with 3M HCl solution to pH < 7. The precipitated solid product was collected by filtration, washed with cold water and dried under vacuum. The crude product can be purified by column chromatography or recrystallized from a suitable solvent system to afford the target compound 4-(4-hydroxy-3-methoxyphenyl)but-3-en-2-one (7a1-d1,7e and 7f).

References

[1] ISMAIL RAHATH KUBRA. Structure-function activity of dehydrozingerone and its derivatives as antioxidant and antimicrobial compounds[J]. Journal of Food Science and Technology, 2011, 51 2: 245-255. DOI:10.1007/s13197-011-0488-8
[2] NORIKO MOTOHASHI . Inhibitory effects of dehydrozingerone and related compounds on 12-O-tetradecanoylphorbol-13-acetate induced Epstein–Barr virus early antigen activation[J]. Cancer letters, 1998, 134 1: Pages 37-42. DOI:10.1016/s0304-3835(98)00239-0
[3] SHINGO YOGOSAWA. Dehydrozingerone, a Structural Analogue of Curcumin, Induces Cell-Cycle Arrest at the G2/M Phase and Accumulates Intracellular ROS in HT-29 Human Colon Cancer Cells[J]. Journal of Natural Products , 2012, 75 12: 2088-2093. DOI:10.1021/np300465f
[4] YIZHEN LIU. Inhibitory effect of dehydrozingerone on vascular smooth muscle cell function.[J]. Journal of Cardiovascular Pharmacology, 2008, 52 5: 422-429. DOI:10.1097/fjc.0b013e31818aed93

Vanillylidenacetone Preparation Products And Raw materials

Global( 135)Suppliers
Supplier Tel Email Country ProdList Advantage
Shaanxi Xianhe Biotech Co., Ltd
+86-17709210191; +8617709210191 Jerry@xhobio.com China 906 58
ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
+86-13017695106 +86-13676922317 jiuyitime@fdachem.com China 16512 58
Xiamen Shindano Biotechnology Co.,ltd
0592-6266840 15750707980 sales@chemsdano.com China 291 58
BOC Sciences
+1-631-485-4226 inquiry@bocsci.com United States 19936 58
Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
+8613580539051 joe@yuhengpharm.com CHINA 21142 58
TargetMol Chemicals Inc.
+1-781-999-5354; +17819995354 marketing@targetmol.com United States 32466 58
Career Henan Chemica Co
+86-0371-86658258 +8613203830695 laboratory@coreychem.com China 30225 58
Hefei TNJ Chemical Industry Co.,Ltd.
+86-0551-65418671 +8618949823763 sales@tnjchem.com China 34563 58
Win-Win chemical CO., Limited
+86-0086-577-64498589 +86-15355981851 sales@win-winchemical.com China 14304 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9996 58

View Lastest Price from Vanillylidenacetone manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Dehydrozingerone pictures 2026-06-02 Dehydrozingerone
1080-12-2
1kg 0.99 1000kg Shaanxi Xianhe Biotech Co., Ltd
Dehydrozingerone pictures 2026-05-20 Dehydrozingerone
1080-12-2
100% 10g TargetMol Chemicals Inc.
Dehydrozingerone pictures 2026-05-20 Dehydrozingerone
1080-12-2
100% 10g TargetMol Chemicals Inc.
VANILLYLIDENACETONE VANILLYLIDENEACETONE FEMA 3738 4-(4-hydroxy-3-methoxyphenyl)-3-buten-2-on dehydro(o)-paradol 4-(4-HYDROXY-3-METHOXYPHENYL)-3-BUTENE-2-ONE methyl-3-methoxy-4-hydroxystyrylketone mhsk vanillalacetone Vanillideneacetone 3-Buten-2-one, 4-(4-hydroxy-3-methoxyphenyl)- 4-(3-Methoxy-4-hydroxyphenyl)-3-butene-2-one Dehydrogingerone Ferulic methyl ketone Vanillylideneacetone ,98% Dehydrozingerone Vanillylideneacetone 4-(4- hydroxy-3-Methoxyphenyl)-3- butene-2- ketone 4-(4-Hydroxy-3-methoxyphenyl)-3-buten-2-one,predominantly trans Vanillylidenacetone >=98.5% 4-(4-Hydroxy-3-methoxyphenyl)-3-buten-2-one> 4-(4-HYDROXY-3-METHOXYPHENYL)-3-BUTEN-2-ONE USP/EP/BP Vanilllylideneacetone 98%(Pre-trans) 4-(-HYDROXY-3-METHOXYPHENYL)-3-BUTEN-2-ONE 4-(4-HYDROXY-3-METHOXYPHENYL)BUT-3-EN-2-ONE 4-(4-HYDROXY-3-METHOXYPHENYL)-3-BUTEN-2-ONE DEHYDROZINGERONE feruloylmethane VANILLYLIDINE ACETONE 1080-12-2 1080-12-02 CH3COCHCHC6H3OCH3OH C11 to C12 Carbonyl Compounds Building Blocks Ketones Organic Building Blocks Aromatic Ketones (substituted)
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