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ACETOACETIC-o-ANISIDIDE | ||
PRODUCT IDENTIFICATION |
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CAS NO. | 92-15-9 | |
EINECS NO. | 202-131-0 | |
FORMULA | C11H13N1O3 | |
MOL WT. | 207.23 | |
H.S. CODE | 2924.29 | |
TOXICITY | Oral mouse LD50: 2 gm/kg | |
SYNONYMS | O-Acetoacetaniside; o-Methoxyacetoacetanilide | |
N-(2-methoxyphenyl)-3-oxobutanamide; N-(2-methoxyphenyl)-3-oxo-Butanamide; 2'-Methoxyacetoacetanilid (German); 2'-metoxiacetoacetanilida (Spanish); 2'-méthoxyacétoacétanilide (French); | ||
SMILES | 2-Oxetanone, 4-Methylene- Diketene ( 674-82-8) | |
CLASSIFICATION |
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PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE | white crystals | |
MELTING POINT |
85 C | |
BOILING POINT |
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SPECIFIC GRAVITY | 1.13 | |
SOLUBILITY | 3 g/L in water | |
pH | ||
VAPOR DENSITY | ||
AUTOIGNITION |
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NFPA RATINGS | Health: 1; Flammability: 1; Reactivity: 0 | |
REFRACTIVE INDEX |
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FLASH POINT | 157 C | |
STABILITY | Stable under normal temperatures and conditions | |
APPLICATIONS |
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Acetoacetic acid derivatives with
heterocycles have
versatile applications including making agrochemicals, dyes,
pigments, pharmaceuticals including vitamins, and
stabilizers for PVC and polyester. They
are used as solvents for fragrances. Acetoacetic acid
and its esters contain
active methylene groups which have relatively acidic alpha-protons due to H
atoms adjacent to two carbonyl groups. The reactivity of its methylene group
provide the sequence of reactions of alkylation, hydrolysis of the esters and
decarboxylation resulting in substituted ketones. The
methylene group can be reacted to form amino-carbonyl compounds.
Acetoacetates
are important aliphatic parts adjoining azo dyes and pigments. Acetoacetic acid is unstable and
decompose to acetone and carbon dioxide at room temperature.
Aacetoacetate is one
of ketone bodies which are the end-products of rapid or excessive fatty acid
breakdown in the human body.
Acetoacetates have a reactive hydrogen atom on the carbon alpha to both carbonyl groups. It undergoes Knoevenagel condensation reaction as a reactant to forms a large class of target products including amino acids, drugs, colorants, lacquers, perfumes, and plastics. Alone, it is used as a flavoring agent and a solvent. Knoevenagel condensation is a nucleophilic addition of a reactive hydrogen atom at 1,3-diketone compounds to a carbonyl group, followed by an dehydration reaction. 1,3-Diketone compounds (beta-ketones) include malonic acid, diethyl malonate, Meldrum's acid, and acetoacetic acid derivatives. AAOT is used in manufacturing agricultural chemicals, coating materials, dyes and pigments, pharmaceuticals, co-promoters for polymers. Anilide is a amide in which one or more hydrogens are replaced by phenyl; having the C6H5NH2-group. Acetoacetaniside is an intermediate for organic yellow pigments, diazo pigment complex with bisdiazonium salt compounds. Anisic acid, p-methoxybenzoic acid, is a part of cresol class antiseptic compounds. It is also used as an insect repellent and ovicide. Anisole, anisic acid, and their deivatives are also widely used in chemical reaction as intermediates to obtain target materials such as dyes, pharmaceuticals, perfumes, photoinitiators and agrochemcials. |
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SALES SPECIFICATION | ||
APPEARANCE |
White to Off-White Powder | |
ASSAY | 99.0% min | |
WATER |
0.2% max | |
MELTING POINT | 83 C min | |
TRANSPORTATION | ||
PACKING | 50 kgs in Fiber drum, 25kgs in Bag | |
HAZARD CLASS | ||
UN NO. | ||
OTHER INFORMATION | ||
Hazard Symbols: XN, Risk Phrases: 22, Safety Phrases: 23-24/25-28A-36-37-45 |
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