| Identification | More | [Name]
Benzalacetone | [CAS]
122-57-6 | [Synonyms]
1-PHENYL-1-BUTEN-3-ONE
4-PHENYL-3-BUTEN-2-ONE
ACETOCINNAMONE
BENZALACETONE
BENZALAOETONE
BENZYLIDENEACETONE
CINNAMYL METHYL KETONE
FEMA 2881
METHYL STYRYL KETONE
TRANS-4-PHENYL-3-BUTEN-2-ONE
TRANS-4-PHENYL-3-BUTENE-2-ONE
TRANS-BENZALACETONE
TRANS-BENZYLIDENEACETONE
(3E)-4-Phenyl-3-buten-2-one
1-Buten-3-one-1-phenyl
2-Phenylvinyl methyl ketone
4-phenyl-3-buten-2-on
4-Phenyl-but-3-en-2-one
4-Phenylbut-3-en-2-one
4-Phenylbutenone | [EINECS(EC#)]
204-555-1 | [Molecular Formula]
C10H10O | [MDL Number]
MFCD00008779 | [Molecular Weight]
146.19 | [MOL File]
122-57-6.mol |
| Chemical Properties | Back Directory | [Appearance]
Yellow Solid | [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 | [refractive index ]
1.5836 | [Fp ]
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]
at 1.00 % in dipropylene glycol. sweet spice cinnamon balsam rhubarb creamy floral | [Odor Type]
spicy | [Water Solubility ]
1.398g/L(25 ºC) | [Sensitive ]
Light Sensitive | [JECFA Number]
820 | [Merck ]
14,1137 | [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]
122-57-6(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin .
R43:May cause sensitization by skin contact.
R42/43:May cause sensitization by inhalation and skin contact . | [Safety Statements ]
S7:Keep container tightly closed .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S37/39:Wear suitable gloves and eye/face protection .
S24:Avoid contact with skin .
S36/37:Wear suitable protective clothing and gloves .
S22:Do not breathe dust . | [WGK Germany ]
3 | [RTECS ]
EN0330050 | [F ]
8 | [TSCA ]
Yes | [HS Code ]
29143900 | [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. |
| Questions And Answer | Back Directory | [Flavorants]
Our GB2760-1996 provisions temporarily allow benzalacetone as a food spice, it is used to modulate sweet pea, cocoa, nuts, cherries, fruit flavor aroma, also used as floral flavor variable swap and anti-propellant, because of the stimulating effect on the skin, it is generally not used in cosmetics. Also benzalacetone can also be used as a mordant, fixing agent and preparation galvanized credit agent in dyeing industry. Credit agent is an organic compound capable of producing bright and leveling effect. Usually it contains aromatic aldehydes or ketones and certain heterocyclic aromatic aldehydes, ie coumarin, vanillin, benzalacetone, its molecular structure contains a carbonyl group, just keeps this structure intact, substituting various substituents, it can produce many kinds of compounds having light effects. Among these, benzalacetone displays best effects, domestic commercial additives are mostly based on such benzalacetone predominating brightener. The most commonly used method is based on the preparation of benzaldehyde and acetone as raw materials, to carry out the Claisen reaction, in the presence of a base (sodium hydroxide or sodium carbonate), aldehydes and ketones condensate, after completing the reaction, diluted hydrochloric acid is added and adjusted to pH = 6-7, set still for stratification, the upper yellow oil is separated, in order to maximize the yield, the lower layer is extracted with benzene, the extract is dried after recovery of benzene, and the oil is combined, then washed with water, separate the oil , bleached with activated carbon, filtered, and purified by vacuum steam distillation, cooled and crystallized, to get crude benzalacetone .
Benzalacetone is also known as 4-phenyl-3-butene-2-one, dibenzylideneacetone, cinnamyl methyl ketone, benzal acetone, methyl styryl ketone. The product abtained by vacuum distillation system is colorless to pale yellow shiny lamellae. It owns sweet pea fragrance and spicy and pungent flavor, changes to deep color exposed in light, combustible, prolonged heat leading to decomposition. Naturally it presents in hydrolyzed soy protein. The formations include cis and trans. Relative molecular mass is 146.19. The relative density is 1.0076 (47.3 ℃). The freezing point is 39 ℃, the melting point is 42 ℃. The boiling point is 261 ℃, 211 ℃ (26.664 × 103Pa), 187.8 ℃ (13.332 × 103Pa), 161.3 ℃ (5.333 × 103Pa), 143.8 ℃ (2.666 × 103Pa), 127.4 ℃ (1.333 × 103Pa), 112.2 ℃ (0.666 × 103Pa ), 81.7 ℃ (0.133 × 103Pa). The refractive index is 1.5836 (45.9 ℃). It is slightly soluble in water and petroleum ether, slightly soluble in benzene, soluble in ethanol, benzene, ether, chloroform and sulfuric acid. It displays a reddish color while reacting with sulfuric acid, this feature can be used to detect the product.
The above information is edited by the Chemicalbook of Tian Ye.
| [Toxicity]
LD50 orally in Rabbit: 2031 mg/kg | [Application limitation]
FEMA (mg/kg): Soft drinks 0.82 ; cold drinks 0.84; confectionery 3.7; bakery 4.5;jelly and pudding 2.1 ; shortening 0.20.
| [Chemical Properties]
It is colorless crystals. It has a coumarin odor. It is soluble in alcohol, ether, benzene and chloroform, slightly soluble in water and petroleum ether.
| [Uses]
1. It is used for the preparation of spices and galvanized brightener.
2. GB 2760--1996 allows it used as food with spices. Formulated balm, cherries, grapes, berries, anise-based and other flavors for temporary .
3. This product is used as galvanized additives, coating materials to increase the brightness. The dyeing industry uses it as a mordant in dyeing agent to improve the uniformity and firmness, also it can be used for the preparation of spices and flavoring agents.
4. 4-phenyl-butene (3)one-2 is one rodenticide warfarin intermediates.
5. As an aromatic organic substance, it is the most widely superior light additive in acid zinc plating process , in the potassium chloride, ammonium plating process, it can get bright coating in a very wide current density and the temperature range, play a good effect on the coating of the internal stress, anti-corrosion ability. This product is also available anti volatile agent for spices, mordant and fixing agent in dyeing industry, it can also be used to prepare spices flavoring agent.
6. Organic synthesis intermediates. It can be used as a spice anti propellant. In dyeing industry,it is used as mordant , fixing agent, it is used for the preparation of spices or flavoring agents, and preparation for galvanized credit agent.
| [Production method]
Using Benzaldehyde for raw materials, and carrying out condensation reaction with acetone . Benzaldehyde and acetone, mixed with water, cooled slowly, added 10% sodium hydroxide solution, the temperature controlled at 25-31°C, After the addition, the stirring was continued for 1h. Then diluted hydrochloric acid was added to pH 6-7, set still for 1h, isolated as a yellow oil. Lower layer was extracted with benzene, the extract and oil were combined, washed twice with water, after the separation the layer of water, recovered benzene, and then dried over calcium chloride, dry decolorizing charcoal was added , filtered and the filtrate vacuum distillation derived products. . Fixed material consumption : benzaldehyde 1700kg/t, acetone 2900kg/t, caustic soda (40%) 500kg/t.
|
| Hazard Information | Back Directory | [Occurrence]
Reported found in hydrolyzed soy protein, soybeans and Virginia tobacco. | [Application]
Benzalacetone(122-57-6) 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.
| [Definition]
ChEBI: An enone in which a phenyl ring is attached to the beta-carbon atom of but-3-en-2-one. Although both cis- and trans-isomers are possible for the alpha,beta-unsaturated ket
ne, only the trans-isomer is observed. | [Preparation]
By condensing benzaldehyde and acetone in the presence of an alkaline condensing agent. | [Aroma threshold values]
Aroma characteristics at 1.0%: sweet, fruity and jamy cherry-like, aldehydic cinnamon spicy, herbal,
anisic, balsamic, toasted almond nutty and woody with slight powdery vanilla nuances. | [Taste threshold values]
Taste characteristics at 5 to 10 ppm: aldehydic, coumarinic and balsamic, slightly nutty, floral and fruity
with woody nuances. | [Synthesis Reference(s)]
The Journal of Organic Chemistry, 58, p. 5595, 1993 DOI: 10.1021/jo00073a011
Tetrahedron Letters, 28, p. 913, 1987 DOI: 10.1016/S0040-4039(00)95872-6 | [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. | [Biochem/physiol Actions]
Taste at 5-10 ppm | [storage]
Store at -20°C | [Purification Methods]
Crystallise it from pet ether (b 40-60o), or distil it (b 137-142o /16mm). [Beilstein 7 IV 1003.] |
|
|