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Цис-3-гексен-1-ол
- английское имяLeaf alcohol
- CAS №928-96-1
- CBNumberCB8723819
- ФормулаC6H12O
- мольный вес100.16
- EINECS213-192-8
- номер MDLMFCD00063217
- файл Mol928-96-1.mol
химическое свойство
Температура плавления | 22.55°C (estimate) |
Температура кипения | 156-157 °C(lit.) |
плотность | 0.848 g/mL at 25 °C(lit.) |
плотность пара | 3.45 (vs air) |
давление пара | 2.26hPa at 25℃ |
показатель преломления | n |
FEMA | 2563 | CIS-3-HEXENOL |
Fp | 112 °F |
температура хранения | Flammables area |
растворимость | DMSO: 100 mg/mL (998.40 mM) |
форма | Liquid |
пка | 15.00±0.10(Predicted) |
Удельный вес | 0.848 (20/4℃) |
цвет | APHA: ≤100 |
Запах | at 10.00 % in dipropylene glycol. fresh green cut grass foliage vegetable herbal oily |
Odor Type | green |
Биологические источники | synthetic |
Вязкость | 3.91mm2/s |
Растворимость в воде | INSOLUBLE |
Мерк | 14,4700 |
Номер JECFA | 315 |
БРН | 1719712 |
Стабильность | Stable. Substances to be avoided include strong oxidizing agents and strong acids. Flammable. |
LogP | 1 at 35℃ |
Вещества, добавляемые в пищу (ранее EAFUS) | CIS-3-HEXEN-1-OL |
Справочник по базе данных CAS | 928-96-1(CAS DataBase Reference) |
FDA UNII | V14F8G75P4 |
Справочник по химии NIST | 3-Hexen-1-ol, (Z)-(928-96-1) |
Система регистрации веществ EPA | (Z)-3-Hexen-1-ol (928-96-1) |
UNSPSC Code | 85151701 |
NACRES | NA.24 |
больше
Коды опасности | F | |||||||||
Заявления о рисках | 10 | |||||||||
Заявления о безопасности | 16 | |||||||||
РИДАДР | UN 1987 3/PG 3 | |||||||||
WGK Германия | 1 | |||||||||
RTECS | MP8400000 | |||||||||
F | 10 | |||||||||
TSCA | Yes | |||||||||
Класс опасности | 3 | |||||||||
Группа упаковки | III | |||||||||
кода HS | 29052990 | |||||||||
Банк данных об опасных веществах | 928-96-1(Hazardous Substances Data) | |||||||||
Токсичность | The acute oral LD50 value in rats was reported as 4.70 g/kg (3.82-5.58 g/kg) (Moreno, 1973). The acute dermal LD50 value in rabbits was reported as > 5 g/kg (Moreno, 1973). | |||||||||
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
H226:Воспламеняющаяся жидкость. Пары образуют с воздухом взрывоопасные смеси.
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оператор предупредительных мер
P210:Беречь от тепла, горячих поверхностей, искр, открытого огня и других источников воспламенения. Не курить.
P240:Заземлить и электрически соединить контейнер и приемное оборудование.
P241:Использовать взрывобезопасное оборудование и освещение.
P303+P361+P353:ПРИ ПОПАДАНИИ НА КОЖУ (или волосы): Снять/удалить немедленно всю загрязненную одежду. Промыть кожу водой.
Цис-3-гексен-1-ол химические свойства, назначение, производство
Описание
Leaf alcohol exists as a liquid at room temperature with a characteristic odor of green leaves. It is found in green tea, violet leaf oil, and many types of leaves, herbs, and grasses. Leaf alcohol finds applications in perfumery as floral fragrance. Leaf alcohol is also investigated for its antidiabetic activity.Химические свойства
Leaf Alcohol is a colorless liquid with the characteristic odor of freshly cut grass. In small quantities, leaf alcohol occurs in the green parts of nearly all plants. The volatile flavor constituents of green tea contain up to 30%.A stereospecific synthesis of (Z)-3-hexen-1-ol starts with the ethylation of sodium acetylide to 1-butyne, which is reacted with ethylene oxide to give 3-hexyn-1-ol. Selective hydrogenation of the triple bond in the presence of palladium catalysts yields (Z)-3-hexen-1-ol. Biotechnological processes have been developed for its synthesis as a natural flavor compound, for example.
Leaf alcohol is used to obtain natural green top notes in perfumes and flavors. In addition, it is the starting material for the synthesis of (2E,6Z)-2,6-nonadien-l-ol and (2E,6Z)-2,6-nonadien-l-al.
Вхождение
Main constituent of the oil distilled from the infusion of fermented tea leaves. Reported found as the corresponding ester of phenylacetic acid in the oil of Japanese mint (Mentha arvensis); the volatile oil of Thea chinensis contains approximately 26 to 35% 3-hexen-1-ol, whereas larger amounts are reported in the oils of Morus bombysic, Robinia pseudacacia and Raphanus sativus. Probably occurring also in several green leaves and herbs; reported found in the fruit juices of raspberry, grapefruit and others. Also reported in over 200 foods including apple, apricot, banana, citrus peel oils and juices, berries, guava, mango, grapes, pineapple, cabbage, kohlrabi, celery, cucumber, lettuce, leek, peas, sauerkraut, tomato, ginger, peppermint oil, coconut oil, spearmint oil, mustard, parsley, breads, butter, fish, fish oil, cognac, brandy, cider, sherry, grape wines, tea, soybeans, avocado, olive, passion fruit, plum, rose apple, Malay apple, water apple (Syzigium spp.), beans, marjoram, starfruit, broccoli, pear and apple brandies, figs, brussels sprouts, radish, prickly pear, litchi, dill, lovage, pumpkin, corn oil, malt, laurel, kiwifruit and other sourcesПодготовка
By the reaction of butyne-1 with ethylene oxide and subsequent selective reduction to the eis isomer (Bedoukian, 1967).Определение
ChEBI: A primary alcohol that consists of (3Z)-hex-3-ene substituted by a hydroxy group at position 1.Общее описание
cis-3-Hexen-1-ol is one of the key volatile constituents of green leaf volatiles(GLV) that can act as an attractant to various insects. It is emitted by green plants when they are physically damaged.использованная литература
[1] NPCS Board of Consultants & Engineers, Industrial Alcohol of Technology Handbook, 2010[2] A. Shirwaikar, K. Rajendran and C. Kumar, Oral Antidiabetic Activity of Annona squamosa Leaf Alcohol Extract in NIDDM Rats, Pharmaceutical Biology, 2004, vol. 42, 30-35
Цис-3-гексен-1-ол запасные части и сырье
Цис-3-гексен-1-ол поставщик
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