Dibenzoyl methane

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Category:Paint chemicals   MOQ:100KG  Shipped directly from China

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Introduction

CAS No. 120-46-7

Content 99%

Packing 25kg/bag

Names and Identifiers

Name Dibenzoylmethane
Synonyms DBM
Dppd-H
rhodiastab83
Dibenzoylmethane
phenylphenacylketone
1,3-Diphenylpropanedione
Phenyl-hydroxystyrylketone
1,3-diphenyl-3-propanedione
1,3-Diphenyl-1,3-propanedione
,3-Diphenyl-propane-1,3-dione
1,3-Diphenylpropane-1,3-dione
1,3-Diphenyl-1,3-propanediamine
(2Z)-3-hydroxy-1,3-diphenylprop-2-en-1-one
CAS 120-46-7
EINECS 204-398-9
InChI InChI=1/C15H12O2/c16-14(12-7-3-1-4-8-12)11-15(17)13-9-5-2-6-10-13/h1-11,16H/b14-11-
InChIKey NZZIMKJIVMHWJC-UHFFFAOYSA-N

120-46-7 – Physico-chemical Properties

Molecular Formula C15H12O2
Molar Mass 224.25
Density 0.800 g/cm3
Melting Point 77-79°C(lit.)
Boling Point 219-221°C18mm Hg(lit.)
Flash Point 219-221°C/18mm
Water Solubility It is Soluble in ether, chloroform, and aqueous sodium hydroxide. Insoluble in water.
Solubility Chloroform (Slightly), Methanol (Slightly, Sonicated)
Vapor Presure 0.01Pa at 20℃
Appearance White to yellow powder or crystal
Color Light yellow to yellow
Merck 14,3009
BRN 514910
pKa 8.95±0.10(Predicted)
Storage Condition Store below +30°C.
Stability Stable. Incompatible with strong oxidizing agents.
Refractive Index 1.6600 (estimate)
MDL MFCD00003085
Physical and Chemical Properties Melting Point: 76-80 ℃
Appearance: white, light yellow crystalline powder
Use As a co-stabilizer for the calcium/zinc hydroxy acid salt stabilization system, used in the manufacture of PVC mineral water bottles
In vitro study Dibenzoylmethane (10, 20, 30, 40, 50 μM; 6 hours) treatment concentration-dependently increases the mRNA level of HO-1 but has no effect on the mRNA level of Nrf2 in HepG2 cells. Dibenzoylmethane induces HO-1 and Nrf2 protein expression, and the induction diminishes after 12 h. Dibenzoylmethane (10, 20, 30, 40, 50 μM; 2 hours) concentration-dependently increases the phosphorylated protein levels of Erk1/2, p38MAPK, JNK, AMPK, and Akt in HepG2 cells. Dibenzoylmethane does not show significant cytotoxicity.
In vivo study Dibenzoylmethane (200, 500 mg/kg/day; ip; for three consecutive days) pretreatment significantly reduces both the area and the severity of necrosis, as well as the leukocyte infiltration, at a dose of 200 mg/kg in wild-type and Nrf2 knockout mice. Dibenzoylmethane protectes against CCl4-induced (1:49,v/v, 10 ml/kg) liver damage in wild-type mice.

120-46-7 – Risk and Safety

Hazard Symbols Xi – Irritant
Risk Codes 36/37/38 – Irritating to eyes, respiratory system and skin.
Safety Description S22 – Do not breathe dust.
S24/25 – Avoid contact with skin and eyes.
WGK Germany 3
RTECS TZ1930000
TSCA Yes
HS Code 29143900
Hazard Note Irritant

Reference Information

LogP 4.59 at 25℃
biological activity Dibenzoylmethane is a minor component in licorice, which can activate Nrf2 and prevent various cancers and oxidative damage. Dibenzoylmethane is an analog of curcumin that causes the dissociation of Keap1 and the nuclear translocation of Nrf2.
use analytical reagent, verification of carbon disulfide and thallium, weight determination of uranium, photometric determination of U 4, extraction of silver, aluminum, barium, beryllium, calcium, cadmium, cobalt, copper, iron, gallium, mercury, lanthanum, magnesium, manganese, nickel, lead, palladium, scandium, thorium, titanium, zinc, zirconium, etc.
As a co-stabilizer of calcium/zinc hydroxy salt stabilization system, used to make PVC mineral water bottles
Production method It is obtained by bromination and hydrolysis from benzylidene acetyl benzene as raw material.

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