W291218
胡椒醇醋酸酯
≥99%, FG
别名:
heliotropyl acetate
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关于此项目
经验公式（希尔记法）:
C10H10O4
化学文摘社编号:
分子量:
194.18
FEMA Number:
2912
Council of Europe no.:
2068
UNSPSC Code:
12164502
PubChem Substance ID:
Flavis number:
9.220
EC Number:
206-312-5
NACRES:
NA.21
MDL number:
Organoleptic:
floral; sweet
Grade:
FG
Biological source:
synthetic
Agency:
meets purity specifications of JECFA
Food allergen:
no known allergens
产品名称
胡椒醇醋酸酯, ≥99%, FG
SMILES string
CC(=O)OCc1ccc2OCOc2c1
InChI key
PFWYHTORQZAGCA-UHFFFAOYSA-N
InChI
1S/C10H10O4/c1-7(11)12-5-8-2-3-9-10(4-8)14-6-13-9/h2-4H,5-6H2,1H3
biological source
synthetic
grade
FG
agency
meets purity specifications of JECFA
reg. compliance
EU Regulation 1334/2008 & 872/2012
FDA 21 CFR 172.515
assay
≥99%
refractive index
n20/D 1.5265 (lit.)
bp
150-151 °C/10 mmHg (lit.)
density
1.227 g/mL at 25 °C (lit.)
application(s)
flavors and fragrances
documentation
see Safety & Documentation for available documents
food allergen
no known allergens
organoleptic
floral; sweet
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hcodes
pcodes
Hazard Classifications
Aquatic Chronic 3
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves
D McGinty et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 50 Suppl 2, S358-S362 (2012-03-27)
A toxicologic and dermatologic review of piperonyl acetate when used as a fragrance ingredient is presented. Piperonyl acetate is a member of the fragrance structural group aryl alkyl alcohol simple acid esters (AAASAE). The AAASAE fragrance ingredients are prepared by
D J Wright et al.
Xenobiotica; the fate of foreign compounds in biological systems, 10(4), 265-270 (1980-04-01)
1. The metabolism of piperonylidene acetone, and the food additives piperonyl acetone, piperonyl acetate and piperonyl isobutyrate were studied in male rabbits after oral doses of 100 mg/kg. 2. Both piperonylidene acetone and piperonyl acetone were extensively excreted as 4-(3,4-methylenedioxyphenyl)-butan-2-ol
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