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Merck

W309109

Sigma-Aldrich

γ-十一内酯

≥98%, FCC, FG

别名:

桃醛, 十四醛

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About This Item

经验公式(希尔记法):
C11H20O2
CAS号:
分子量:
184.28
FEMA號碼:
3091
EC號碼:
歐洲委員會號碼:
179
MDL號碼:
分類程式碼代碼:
12164502
PubChem物質ID:
Flavis號碼:
10.002
NACRES:
NA.21

生物源

synthetic

品質等級

等級

FG
Fragrance grade
Halal
Kosher

agency

follows IFRA guidelines
meets purity specifications of JECFA

法律遵循

EU Regulation 1223/2009
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 172.515

化驗

≥98%

折射率

n20/D 1.45 (lit.)

bp

164-166 °C/13 mmHg (lit.)

密度

0.949 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

香料過敏原

no known allergens

感官的

coconut; creamy; fatty; fruity; peach

SMILES 字串

CCCCCCCC1CCC(=O)O1

InChI

1S/C11H20O2/c1-2-3-4-5-6-7-10-8-9-11(12)13-10/h10H,2-9H2,1H3

InChI 密鑰

PHXATPHONSXBIL-UHFFFAOYSA-N

基因資訊

human ... CYP1A2(1544)

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一般說明

γ-Undecalactone is a volatile flavor constituent found in low-fat ice cream.

應用


  • Investigation of Lactone Chiral Enantiomers and Their Contribution to the Aroma of Longjing Tea by Odor Activity Value and S-Curve.: This study explores the chiral enantiomers of lactones, including γ-Undecalactone, and their impact on the aroma profile of Longjing tea, using odor activity value and S-curve methods to quantify their contributions (Zhu et al., 2023).

危險聲明

防範說明

危險分類

Aquatic Chronic 3

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 1

閃點(°F)

293.0 °F - closed cup

閃點(°C)

145 °C - closed cup

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Total phenolic compounds, antioxidant activity and nutritional values of sugar-free and reduced-fat milk-based ice cream enriched with selected herb ingredients.
Limsuwan T.
Asia-Pacific Journal of Science and Technology , 19(4), 515-525 (2017)
Laura E Korhonen et al.
Journal of medicinal chemistry, 48(11), 3808-3815 (2005-05-27)
The purpose of this study was to determine the cytochrome P450 1A2 (CYP1A2) inhibition potencies of structurally diverse compounds to create a comprehensive three-dimensional quantitative structure-activity relationship (3D-QSAR) model of CYP1A2 inhibitors and to use this model to predict the

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