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DODECYL ACETATE

CAS No.112-66-3
Chemical Name:DODECYL ACETATE
CBNumber:CB1481796
Molecular Formula:C14H28O2
Formula Weight:228.37
MOL File:112-66-3.mol

DODECYL ACETATE Property

Melting point 1.3℃
Boiling point 150 °C15 mm Hg(lit.)
Density 0.865 g/mL at 25 °C(lit.)
refractive index n20/D 1.432(lit.)
FEMA 2616 | LAURYL ACETATE
Flash point >230 °F
storage temp. Sealed in dry,Room Temperature
solubility Acetone (Slightly), Chloroform (Slightly), Hexanes (Slightly)
form Oil
color Colourless
Odor at 100.00 %. sweet fresh laundared cloths clean waxy
Odor Type waxy
biological source synthetic
JECFA Number 133
LogP 6.02
CAS DataBase Reference 112-66-3(CAS DataBase Reference)
Substances Added to Food (formerly EAFUS) LAURYL ACETATE
FDA 21 CFR 172.515
EWG's Food Scores 1
FDA UNII 76J36KE44B
EPA Substance Registry System Acetic acid, dodecyl ester (112-66-3)
UNSPSC Code 12352100
NACRES NA.22

Safety

Risk Statements :53
WGK Germany :2
RTECS :AH3525000
HS Code :2915.39.4000

NFPA 704:

	1
0		0

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal wordWarning
Hazard statements H227-H315
Precautionary statements P210-P280-P370+P378-P403+P235-P501

DODECYL ACETATE Price More Price(6)

Brand: Sigma-Aldrich(India)
Product number: W261602
Product name : Lauryl acetate
Purity: ≥98%, FG
Packaging: 1SAMPLE-K
Price: ₹4990.33
Updated: 2022/06/14
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Brand: Sigma-Aldrich(India)
Product number: W261602
Product name : Lauryl acetate
Purity: ≥98%, FG
Packaging: 1KG
Price: ₹14970.98
Updated: 2022/06/14
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Brand: Sigma-Aldrich(India)
Product number: W261602
Product name : Lauryl acetate
Purity: ≥98%, FG
Packaging: 4KG
Price: ₹45367.58
Updated: 2022/06/14
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Brand: Sigma-Aldrich(India)
Product number: D221953
Product name : Dodecyl acetate
Purity: 97%
Packaging: 25G
Price: ₹6202.73
Updated: 2022/06/14
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Brand: TCI Chemicals (India)
Product number: A0902
Product name : Dodecyl Acetate
Purity: min. 97.0 %
Packaging: 25ML
Price: ₹2300
Updated: 2022/05/26
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DODECYL ACETATE Chemical Properties,Usage,Production

Description Lauryl acetate has a characteristic citrus-rose odor. The corre sponding flavor develops only on dilution. May be prepared by acetylation of lauryl alcohol.
Chemical Properties Lauryl acetate has a characteristic citrus–rose odor. The corresponding flavor develops only on dilution.
Occurrence Reported found in sour cherry, cardamom, bitter orange, lime, lemon and mandarin peel oils.
Uses 1-Dodecanol Acetate can be used as a foaming agent in the purification process of quartz sand. Furthermore, it is a main component of the essential oil from the flowers of Etlingera elatior (Jack) R. M. Smith, which is found to be active against Staphylococcus aureus, Bacillus cereus, Candida albicans and Cryptococcus neoformans.
Definition ChEBI: Dodecyl acetate is a carboxylic ester.
Application Dodecyl acetate is useful in perfume formulations, particularly as a topnote ingredient - in spite of its high boiling point. In fact, the performance of odor, shown by this chemical, is quite remarkable. A lasting odor from the very topnote throughout the various stages of evaporation of the fragrance. However, it needs blending with other materials to become more attractive, especially Citrus oils, light, fruity notes or light woody notes. It will also impart a pleasant freshness to sophisticated Pine fragrances, and in Carnation bases. Dodecyl acetate is also used in flavor compositions for imitation Butter, Lemon, Orange, Peach, Pineapple, etc. and in various meat flavor bases. The concentration in the finished product will normally be about 1 to 6 ppm.
Preparation By acetylation of lauryl alcohol.
Synthesis Reference(s) The Journal of Organic Chemistry, 38, p. 764, 1973 DOI: 10.1021/jo00944a031
Synthesis, p. 309, 1971
Toxicity evaluation Both the acute oral LD₅₀ value in rats and the acute dermal LD₅₀ value in rabbits exceeded 5 g/kg (Moreno, 1974). In a study of toxicity to fish, the toxic concentration of lauryl acetate to Carassius auratus and Salmo gairdnerii during a 6-hr observation period at 15°C was found to be 5.20 mg/litre.The surface tension (50.1) was not related directly to the toxicity (Marchetti, 1964).