추천 제품
생물학적 소스
synthetic
Quality Level
Grade
FG
Halal
Kosher
Agency
meets purity specifications of JECFA
규정 준수
EU Regulation 1334/2008 & 872/2012
FDA 21 CFR 172.515
vapor pressure
0.01 mmHg ( 25 °C)
분석
≥98%
bp
260-262 °C (lit.)
mp
39-42 °C (lit.)
응용 분야
flavors and fragrances
문건
see Safety & Documentation for available documents
식품 알레르기항원
no known allergens
감각 수용성의
anise; cinnamon; jam; balsamic; spicy; floral; sweet
SMILES string
[H]\C(=C(\[H])c1ccccc1)C(C)=O
InChI
1S/C10H10O/c1-9(11)7-8-10-5-3-2-4-6-10/h2-8H,1H3/b8-7+
InChI key
BWHOZHOGCMHOBV-BQYQJAHWSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
일반 설명
Benzylideneacetone is used in the fragrance industry for its sweet pea-like odor. It is one of the major constituents of Monanthotaxis capea essential oil. Studies suggest that apart from skatole and androstenone, benzylideneacetone may also be one of the volatile compounds, which contributes to the development of boar taint in fat samples.
생화학적/생리학적 작용
Taste at 5-10 ppm
기타 정보
Natural occurrence: Soybeans and Virginia tobacco.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Skin Irrit. 2 - Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 2
Flash Point (°F)
253.4 °F - closed cup
Flash Point (°C)
123 °C - closed cup
개인 보호 장비
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
이미 열람한 고객
Phenylbutane Derivatives as Main Constituents of Monanthotaxis capea Essential Oil.
J. Essent. Oil Res., 4(1), 33-39 (1992)
Role of 4-phenyl-3-buten-2-one in boar taint: identification of new compounds related to sensorial descriptors in pig fat.
Journal of Agricultural and Food Chemistry, 49(11), 5303-5309 (2001)
Organic & biomolecular chemistry, 10(6), 1239-1245 (2011-12-20)
An efficient and easy procedure to synthesize the pyridinyl analogues of dibenzylideneacetone (pyr-dba) was developed by the condensation of substituted nicotinaldehyde and acetone in the presence of K(2)CO(3) in toluene-EtOH-H(2)O solvent system. Structurally diverse pyr-dba, including quinolinyl dba, can be
The Journal of organic chemistry, 71(7), 2918-2921 (2006-03-25)
The first efficient asymmetric synthesis of obolactone 1 has been accomplished in 11 steps and with a 15% overall yield in which Brown's enantioselective allylation reactions and ring-closing metathesis reaction are key steps.
Highly asymmetric Michael addition to alpha,beta-unsaturated ketones catalyzed by 9-amino-9-deoxyepiquinine.
Angewandte Chemie (International ed. in English), 46(3), 389-392 (2006-12-13)
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