NOOTKATONE

한글명:NOOTKATONE

카스 번호4674-50-4

상품명:NOOTKATONE

CBNumberCB3751288

분자식C15H22O

포뮬러 무게218.33

MOL 파일4674-50-4.mol

화학적 성질

녹는점	35-39 °C
끓는 점	125°C 0,5mm
밀도	0,997 g/cm³
FEMA	3166 \| NOOTKATONE
굴절률	n20/D 1.52
인화점	99°C
저장 조건	2-8°C
용해도	클로로포름(약간 용해됨), 에탄올(약간 용해됨), 메탄올(약간 용해됨)
물리적 상태	Solid
색상	흰색에서 연한 노란색
냄새	100.00%에서. 자몽 껍질 감귤류 치자나무 우디
?? ??	감귤류
optical activity	[α]20/D +182.0±5.0°, c = 1% in ethanol
수용성	에탄올과 클로로포름에 약간 용해됩니다. 물에 부분적으로 용해됩니다.
JECFA Number	1398
BRN	4676969
안정성	안정적인. 강한 산화제와 호환되지 않습니다.
InChIKey	WTOYNNBCKUYIKC-UHFFFAOYSA-N
LogP	3.84
EPA	2(3H)-Naphthalenone, 4,4a,5,6,7,8-hexahydro-4,4a-dimethyl-6-(1-methylethenyl)-, (4R,4aS,6R)- (4674-50-4)

위험 및 안전 성명

안전지침서

23-24/25

WGK 독일

TSCA

Yes

HS 번호

29142990

유해 물질 데이터

4674-50-4(Hazardous Substances Data)

NFPA 704:

	0
0		0

그림문자(GHS)

NOOTKATONE 화학적 특성, 용도, 생산

개요
Nootkatone has a pleasant taste. It may be prepared by oxidation of valencene (a sesquiterpene) with tertiary butyl chromate.
화학적 성질
NOOTKATONE has been isolated from grapefruit peel and juice and identified in other citrus oils as well. The commercially available product is a colorless to yellowish liquid with a typical grapefruit odor.
Nootkatone can be prepared by oxidation of valencene, a sesquiterpene hydrocarbon isolated from orange oils. The oxidation can be accomplished either by chemical or by biotechnological methods.
Nootkatone is used for flavoring beverages.
출처
Reported found in grapefruit oil and juice; traces are also reported found in the oils of bergamot, lemon, lime, orange and tangerine; also reported formed in canned orange juice on storage.
용도
Nootkatone is an effective repellent/insecticide against mosquitos, and may repel bed bugs, head lice and other insects. Nootkatone in spray form has been shown as an effective repellent/insecticide against deer ticks and lone star ticks.
제조 방법
By oxidation of valencene (a sesquiterpene) with tertiary butyl chromate.
정의
ChEBI: A sesquiterpenoid that is 4,4a,5,6,7,8-hexahydronaphthalen-2(3H)-one which is substituted by methyl groups at positions 4 and 4a, and by an isopropenyl group at position 6 (the 4R,4aS,6R stereoisomer).
일반 설명
(+)-nootkatone, a bicyclic conjugated sesquiterpene ketone with a grapefruit-like flavor, is commonly used in fragrance, food, cosmetics and pharmaceutical industry. It can be synthesized from (+)-valencene via biotransformation. (+)-nootkatone is the active ingredient responsible for the antiplatelet effect of Cyperus rotundus, a well-known oriental traditional medicine. It also shows promising efficacy against Staphylococcus aureus biofilms.

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