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Merck

W353205

Sigma-Aldrich

3-癸烯-2-酮

predominantly trans, ≥97%, stabilized, FG

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About This Item

线性分子式:
CH3(CH2)5CH=CHCOCH3
CAS号:
分子量:
154.25
FEMA號碼:
3532
EC號碼:
歐洲委員會號碼:
11751
MDL號碼:
分類程式碼代碼:
12164502
PubChem物質ID:
Flavis號碼:
7.121
NACRES:
NA.21
agency:
meets purity specifications of JECFA

生物源

synthetic

品質等級

等級

FG
Halal
Kosher

agency

meets purity specifications of JECFA

法律遵循

EU Regulation 1334/2008 & 872/2012

化驗

≥97%

包含

α-Tocopherol. synthetic as stabilizer

折射率

n20/D 1.45 (lit.)

bp

125 °C/12 mmHg (lit.)

密度

0.847 g/mL at 25 °C (lit.)

應用

flavors and fragrances

文件

see Safety & Documentation for available documents

食物過敏原

no known allergens

感官的

fatty; green; jasmine; vegetable

SMILES 字串

CCCCCC\C=C\C(C)=O

InChI

1S/C10H18O/c1-3-4-5-6-7-8-9-10(2)11/h8-9H,3-7H2,1-2H3/b9-8+

InChI 密鑰

JRPDANVNRUIUAB-CMDGGOBGSA-N

一般說明

3-Decen-2-one occurs naturally in certain species of mushroom.

應用

Possible applications: Apricot, peach, watermelon, pear, cucumber, and tropical fruits, dairy flavors such as milks creams and cheeses. Fatty notes in chicken, fat replacers and lard. Used in mandarin, tangerine, grapefruit and other citrus flavors.

生化/生理作用

1-5ppm 时的味道

其他說明

天然存在:蘑菇。

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

197.6 °F - closed cup

閃點(°C)

92 °C - closed cup


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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其他客户在看

Slide 1 of 1

1 of 1

Character impact odorants from wild mushroom (Lactarius hatsudake) used in Japanese traditional food.
Miyazawa M, et al.
Flavour and Fragrance Journal, 25(4), 197-201 (2010)
Volatile Composition of Some Cultivated and Wild Culinary-Medicinal Mushrooms from Hungary.
Csoka M, et al.
International Journal of Medicinal Mushrooms, 19(5) (2017)
Svenja Nörenberg et al.
Journal of agricultural and food chemistry, 65(40), 8913-8922 (2017-09-19)
A homologous series of 4-mercapto-2-alkanols (C5-C10) was used to investigate the impact of the stereochemistry on the sensory properties of a class of naturally occurring polyfunctional thiols having a 1,3-oxygen-sulfur functionality. Stereoisomers were obtained via syntheses of racemic mixtures and
Mosciano, G.
Perfumer & Flavorist, 25, 71-71 (2000)

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