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Этил каприла
- английское имяEthyl caprylate
- CAS №106-32-1
- CBNumberCB4852670
- ФормулаC10H20O2
- мольный вес172.26
- EINECS203-385-5
- номер MDLMFCD00009552
- файл Mol106-32-1.mol
химическое свойство
Температура плавления | -48--47 °C (lit.) |
Температура кипения | 206-208 °C (lit.) |
плотность | 0.867 g/mL at 20 °C (lit.) |
давление пара | 0.02 mm Hg ( 25 °C) |
показатель преломления | n |
FEMA | 2449 | ETHYL OCTANOATE |
Fp | 167 °F |
температура хранения | Store below +30°C. |
растворимость | ethanol: soluble1ml/4ml, clear, colorless (70% ethanol) |
форма | Liquid |
цвет | Clear colorless |
Запах | at 100.00 %. fruity wine waxy sweet apricot banana brandy pear |
Odor Type | waxy |
Биологические источники | synthetic |
Пределы взрываемости | 0.7%(V) |
Растворимость в воде | insoluble |
Номер JECFA | 33 |
Мерк | 14,3778 |
БРН | 1754470 |
LogP | 4.47 at 22.7℃ |
Справочник по базе данных CAS | 106-32-1(CAS DataBase Reference) |
Вещества, добавляемые в пищу (ранее EAFUS) | ETHYL OCTANOATE |
FDA 21 CFR | 172.515 |
Рейтинг продуктов питания EWG | 1 |
FDA UNII | 81C5MOP582 |
Справочник по химии NIST | Octanoic acid, ethyl ester(106-32-1) |
Система регистрации веществ EPA | Ethyl octanoate (106-32-1) |
UNSPSC Code | 85151701 |
NACRES | NA.24 |
больше
Коды опасности | Xi | |||||||||
Заявления о рисках | 38 | |||||||||
Заявления о безопасности | 26-36 | |||||||||
WGK Германия | 2 | |||||||||
RTECS | RH0680000 | |||||||||
Температура самовоспламенения | 325 °C | |||||||||
TSCA | Yes | |||||||||
кода HS | 29159080 | |||||||||
Токсичность | LD50 orally in rats: 25,960 mg/kg, P. M. Jenner et al., Food Cosmet. Toxicol. 2, 327 (1964) | |||||||||
NFPA 704: |
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рисовальное письмо(GHS)
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рисовальное письмо(GHS)
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сигнальный язык
предупреждение
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вредная бумага
H411:Токсично для водных организмов с долгосрочными последствиями.
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оператор предупредительных мер
P273:Избегать попадания в окружающую среду.
P391:Ликвидировать просыпания/проливы/утечки.
P501:Удалить содержимое/ контейнер на утвержденных станциях утилизации отходов.
Этил каприла химические свойства, назначение, производство
Описание
Ethyl caprylate (ethyl octanoate) is a kind of fatty acid ester formed from caprylic acid and ethanol. It is a kind of natural fruit flavoring agent. It is usually included in the alcohol beverage. Among the main flavoring components of None-flavor liquor, the absolute content of ethyl caprylate is not high but its flavoring contributions is higher than ethyl acetate, ethyl lactate, and ethyl butyrate, only lower than ethyl caproate. Only small amount of ethyl caprylate could produce obvious fruit aroma in Nong-flavor liquor. However, excessive content of ethyl caprylate would inhibit the performance of other flavoring components.Химические свойства
CLEAR COLOURLESS LIQUIDВхождение
Reported found in apple, apricot, orange juice, grapefruit juice, guava, pineapple, cheddar cheese, other cheeses, butter, beer, cognac, rum, whiskey, cider, grape wines, cocoa, coconut meat, passion fruit, mango, pawpaw and mastic gum leaf oil.Использование
Ethyl caprylate is a flavoring and fragrance agent.Подготовка
Usually prepared by esterification of caprylic acid with ethyl alcohol and sulfuric acid as catalyst; also by alcoholysis of coconut oil in the presence of HCl.Определение
ChEBI: A fatty acid ethyl ester resulting from the formal condensation of octanoic acid with ethanol.Общее описание
Ethyl octanoate is a powerful odourant found in mead (a traditional drink that contains alcohol).Профиль безопасности
Mddly toxic by ingestion. A skin irritant. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS.Канцерогенность
Not listed by ACGIH, California Proposition 65, IARC, NTP, or OSHA.Метаболизм
Aliphatic esters including ethyl caprylate are thought to be readily hydrolysed to the corresponding alcohol and acid, which are then further metabolized (Fassett, 1963). Oral adminis tration of ethyl caprylate to rats produced a ketonuria twice as great as that from acetoacetate, indicating the formation of two fragments for the production of ketone bodies, and it was suggested that caprylic acid was probably broken down by a process involving multiple alternate oxidation (Deuel, Hallman, Butts & Murray, 1936).использованная литература
Powers, John J. "HETEROGENEITY AND TEMPERATURE EFFECTS ON FLAVOR SENSING OF ETHYL CAPRYLATE." Journal of Food Science 42.1(2010):275-276.Zhibin, L. I., and L. I. Jin. "Analysis of the Content of Ethyl Caprylate in Nong-flavor Liquor and Its Flavoring Contributions." Liquor-Making Science & Technology (2013).
Этил каприла запасные части и сырье
Этил каприла поставщик
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Этил каприла Обзор)
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