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Merck
모든 사진(1)

문서

77416

Supelco

Fructone

analytical standard

동의어(들):

Ethyl 2-methyl-1,3-dioxolane-2-acetate, 2-Methyl-1,3-dioxolane-2-acetic acid ethyl ester, Applinal, Ethyl 2-methyldioxolan-2-yl acetate, Jasmaprunat, NSC 6537

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About This Item

실험식(Hill 표기법):
C8H14O4
CAS Number:
Molecular Weight:
174.19
Beilstein:
130164
EC Number:
MDL number:
UNSPSC 코드:
85151701
PubChem Substance ID:
NACRES:
NA.24

Grade

analytical standard

Quality Level

분석

≥99.0% (GC)

유통기한

limited shelf life, expiry date on the label

refractive index

n20/D 1.431-1.435

응용 분야

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

형식

neat

저장 온도

2-8°C

SMILES string

O=C(OCC)CC1(C)OCCO1

InChI

1S/C8H14O4/c1-3-10-7(9)6-8(2)11-4-5-12-8/h3-6H2,1-2H3

InChI key

XWEOGMYZFCHQNT-UHFFFAOYSA-N

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일반 설명

Fructone is an aromatic compound with a strong fruity odor. The olfactory factor is described as pineapple-, strawberry- and apple-like. It is primarily utilized as a fragrance and flavoring material in cosmetics, food and beverages, manufacture of drugs and detergents, and perfume industries.

추천 제품

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point (°F)

199.4 °F

Flash Point (°C)

93 °C


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문서 라이브러리 방문

Sophia C Poletti et al.
Perception, 46(3-4), 343-351 (2016-10-06)
Background Repeated short-term exposure to odors is known to improve olfaction in patients with acquired olfactory dysfunction. The aim was to find out whether differences in molecular weight of odors used for olfactory training influences olfaction. We hypothesized a greater
Preparation of fructone catalyzed by aluminium sulfate in ionic liquid medium
Lin Q, et al.
Journal of Saudi Chemical Society, 15(2), 101-103 (2011)

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