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2-Pentyl-3-methyl-2-cyclopenten-1-one

 структура
1128-08-1
CAS №
1128-08-1
английское имя:
2-Pentyl-3-methyl-2-cyclopenten-1-one
Синонимы:
FEMA 3763;DI JASMONE;DIHYDROJASMON;DIHYDROJASMONE;Jasmone, dihydro-;DIHYDROJASMONE(RG);Dihydrojasmone >Tetrahydroprethrone;DIHYDROJASMONE 98+%;Tetrahy-dropyrethrone
CBNumber:
CB4487865
Формула:
C11H18O
молекулярный вес:
166.26
MOL File:
1128-08-1.mol

2-Pentyl-3-methyl-2-cyclopenten-1-one атрибут

Температура кипения: 120-121 °C12 mm Hg(lit.)
плотность: 0.916 g/mL at 25 °C(lit.)
FEMA: 3763 | 3-METHYL-2-(N-PENTANYL)-2-CYCLOPENTEN-1-ONE
показатель преломления: n20/D 1.479(lit.)
Fp: 230 °F
температура хранения: Store at -20°C
растворимость: DMSO:100.0(Max Conc. mg/mL);601.45(Max Conc. mM)
форма: чистая жидкость
Удельный вес: 0.914~0.916 (20/4℃)
цвет: Бесцветная слегка маслянистая жидкость с цветочным запахом.
Запах: at 100.00 %. fresh outdoor jasmin myrrh woody spice herbal
Odor Type: floral
Номер JECFA: 1406
БРН: 1906471
LogP: 3.25
Справочник по базе данных CAS: 1128-08-1(CAS DataBase Reference)
Вещества, добавляемые в пищу (ранее EAFUS): 2-PENTYL-3-METHYL-2-CYCLOPENTEN-1-ONE
Рейтинг продуктов питания EWG: 1
FDA UNII: Y953R7PP90
Справочник по химии NIST: Dihydrojasmone(1128-08-1)
Система регистрации веществ EPA: 2-Cyclopenten-1-one, 3-methyl-2-pentyl- (1128-08-1)

Заявления о рисках и безопасности

WGK Германия 2
RTECS GY7302000
TSCA Yes
кода HS 29142990
Токсичность The acute oral LD50 in rats was reported as 2.5 g/kg (1.79-3.50 g/kg) (Keating, 1972). The acute dermal LD50 value in rabbits was reported as 5 g/kg (Keating, 1972).

2-Pentyl-3-methyl-2-cyclopenten-1-one MSDS


2-Pentyl-3-methyl-2-cyclopenten-1-one

2-Pentyl-3-methyl-2-cyclopenten-1-one химические свойства, назначение, производство

Химические свойства

2-Pentyl-3-methyl-2-cyclopenten-1-one is a colorless, slightly viscous liquid with a typical jasmine odor, resembling that of the naturally occurring (Z)-jasmone. Dihydrojasmone is produced by an acid-catalyzed rearrangement of 4-methyl-??-decalactone, which is readily obtained by radical addition of 2-octanol to acrylic acid.
Dihydrojasmone is used in perfumery in jasmine bases and, more generally, in floral and fruity fragrances.

Вхождение

Has apparently not been reported to occur in nature.

Подготовка

Hexyl bromide plus levulinic ester yields a lactone, which is reacted with polyphosphoric acid or phosphorus pentoxide to produce hydrojasmone.

2-Pentyl-3-methyl-2-cyclopenten-1-one препаратная продукция и сырье

сырьё

препарат


2-Pentyl-3-methyl-2-cyclopenten-1-one поставщик

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