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Benzalacetone

Benzalacetone Structure
CAS No.
122-57-6
Chemical Name:
Benzalacetone
Synonyms
(E)-4-Phenylbut-3-en-2-one;4-PHENYL-3-BUTEN-2-ONE;benzylidene;BENZYLIDENEACETONE;4-Phenylbut-3-en-2-one;(3E)-4-phenylbut-3-en-2-one;Benzalaceton;3-Buten-2-one, 4-phenyl-;ACETOCINNAMONE;Benzilidine Acetone
CBNumber:
CB3119480
Molecular Formula:
C10H10O
Molecular Weight:
146.19
MOL File:
122-57-6.mol
MSDS File:
SDS
Modify Date:
2024/6/5 16:50:33

Benzalacetone Properties

Melting point 39-42 °C(lit.)
Boiling point 260-262 °C(lit.)
Density 1.038
vapor pressure 0.01 mm Hg ( 25 °C)
FEMA 2881 | 4-PHENYL-3-BUTEN-2-ONE
refractive index 1.5836
Flash point 150 °F
storage temp. Store at <= 20°C.
solubility Soluble in alcohol, chloroform, diethyl ether.
form Low Melting Solid
color Pale yellow to yellow
Odor Sweet, but rather pungent odor with a creamy-floral note.
Odor Type spicy
Water Solubility 1.398g/L(25 ºC)
Sensitive Light Sensitive
Merck 14,1137
JECFA Number 820
BRN 742046
Stability Light Sensitive
InChIKey BWHOZHOGCMHOBV-BQYQJAHWSA-N
LogP 2.04
CAS DataBase Reference 122-57-6(CAS DataBase Reference)
NIST Chemistry Reference 3-Buten-2-one, 4-phenyl-(122-57-6)
EPA Substance Registry System Benzylideneacetone (122-57-6)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H317
Precautionary statements  P280
Hazard Codes  Xn,Xi
Risk Statements  36/37/38-43-42/43
Safety Statements  7-26-36/37/39-45-37/39-24-36/37-22
WGK Germany  3
RTECS  EN0330050
8
TSCA  Yes
HS Code  29143900
Toxicity LD50 orally in Rabbit: 2031 mg/kg
NFPA 704
1
3 1

Benzalacetone price More Price(12)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) W288101 Benzylideneacetone ≥98%, FG 122-57-6 1SAMPLE-K ₹5141.88 2022-06-14 Buy
Sigma-Aldrich(India) W288101 Benzylideneacetone ≥98%, FG 122-57-6 1KG ₹9937.35 2022-06-14 Buy
Sigma-Aldrich(India) W288101 Benzylideneacetone ≥98%, FG 122-57-6 10KG ₹53367.25 2022-06-14 Buy
Sigma-Aldrich(India) W288101 Benzylideneacetone ≥98%, FG 122-57-6 25KG ₹96353.33 2022-06-14 Buy
Sigma-Aldrich(India) 68381 Benzalacetone analytical standard 122-57-6 100MG ₹5260.95 2022-06-14 Buy
Product number Packaging Price Buy
W288101 1SAMPLE-K ₹5141.88 Buy
W288101 1KG ₹9937.35 Buy
W288101 10KG ₹53367.25 Buy
W288101 25KG ₹96353.33 Buy
68381 100MG ₹5260.95 Buy

Benzalacetone Chemical Properties,Uses,Production

Chemical Properties

Yellow Solid

Occurrence

Occasionally Benzalacetone is used in perfumery for Sweet Pea (used to be a “must” in this type of fragrance), in Appleblossom, etc., often in combination with Neroli and Hyacinth bases. Also used in flavors, particularly in Chocolate, Cocoa, Cherry, Fruit, Nut, Vanilla, etc. - but usually at very low concentration. Concentration in finished product will rarely exceed 0.2 to 0.5 ppm.

Uses

brightener in acid zinc electroplating,also used as an organic synthesis intermediate in flavor and fragrance, pharmaceutical industries

Preparation

By condensing benzaldehyde and acetone in the presence of an alkaline condensing agent.

Definition

ChEBI: Trans-benzylideneacetone is the trans-isomer of benzylideneacetone. It acts as an inhibitor of the enzyme phospholipase A2 (EC 3.1.1.4) of insects like diamond back moth. It has a role as a flavouring agent, a fragrance, a bacterial metabolite and an EC 3.1.1.4 (phospholipase A2) inhibitor.

Application

Benzalacetone is an endogenous metabolite. It acts as a flavouring agent, a spice, a bacterial metabolite and an inhibitor of EC 3.1.1.4 (phospholipase A2). It is mainly used in food additives, flavours and fragrances, and as an intermediate in chemical synthesis or reaction reagents. In addition, the novel hydrophobic benzazepine acetone can also be used to modify lead dioxide electrodes for electrocatalytic degradation of coal tar wastewater.

General Description

trans- 4-Phenyl-3-buten-2-one is substrate for glutathione transferase. It reacts with methyl- and benzylguanidine to yield aromatic N2-substituted 2-pyrimidinamines.

Safety Profile

Poison by intravenous route. Moderately toxic by intraperitoneal route. A skin irritant. A flammable liquid. When heated to decomposition it emits acrid smoke and irritating fumes. See also KETONES.

Purification Methods

Crystallise it from pet ether (b 40-60o), or distil it (b 137-142o /16mm). [Beilstein 7 IV 1003.]

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