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经验公式(希尔记法):
C12H22O2
化学文摘社编号:
分子量:
198.30
FEMA Number:
2400
Council of Europe no.:
2240
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
10.019
EC Number:
218-971-6
NACRES:
NA.21
MDL number:
Beilstein/REAXYS Number:
126680
Organoleptic:
coconut; creamy; fatty; fruity; peach; sweet
Grade:
FG
Halal
Kosher
Halal
Kosher
Biological source:
synthetic
Food allergen:
no known allergens
产品名称
γ-十二内酯, ≥97%, FCC, FG
SMILES string
CCCCCCCCC1CCC(=O)O1
InChI
1S/C12H22O2/c1-2-3-4-5-6-7-8-11-9-10-12(13)14-11/h11H,2-10H2,1H3
InChI key
WGPCZPLRVAWXPW-UHFFFAOYSA-N
biological source
synthetic
grade
FG
Halal
Kosher
reg. compliance
EU Regulation 1334/2008 & 178/2002
FCC
FDA 21 CFR 117
assay
≥97%
refractive index
n20/D 1.452 (lit.)
bp
130-132 °C/1.5 mmHg (lit.)
mp
17-18 °C (lit.)
density
0.936 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
coconut; creamy; fatty; fruity; peach; sweet
Gene Information
human ... CYP1A2(1544)
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Application
- Differentiation of Rums Produced from Sugar Cane Juice (Rhum Agricole) from Rums Manufactured from Sugar Cane Molasses by a Metabolomics Approach.: This study uses a metabolomics approach to differentiate between rums made from sugar cane juice and those from molasses, focusing on key flavor compounds such as gamma-dodecalactone. This research provides insight into the flavor chemistry of rum, supporting better understanding of food flavor and authenticity (Franitza et al., 2018).
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
228.2 °F - closed cup
flash_point_c
109 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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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