헥실살리실레이트

한글명:헥실살리실레이트

카스 번호6259-76-3

상품명:Hexyl salicylate

CBNumberCB4430407

분자식C13H18O3

포뮬러 무게222.28

MOL 파일6259-76-3.mol

동의어(한글)

헥실살리실레이트

화학적 성질

끓는 점	290 °C (lit.)
밀도	1.04 g/mL at 25 °C (lit.)
증기압	0.077Pa at 23℃
굴절률	n20/D 1.505(lit.)
인화점	>230 °F
저장 조건	Sealed in dry,Room Temperature
용해도	클로로포름(소량으로 용해), DMSO(약간 용해됨)
산도 계수 (pKa)	8.17±0.30(Predicted)
색상	무색 유성 액체.
냄새	100.00%에서. 신선한 허브 난초 녹색
?? ??	약초
수용성	0.28g/L(37 ºC)
BRN	2453103
LogP	5.5 at 30℃
CAS 데이터베이스	6259-76-3(CAS DataBase Reference)
NIST	N-hexyl salicylate(6259-76-3)
EPA	Hexyl salicylate (6259-76-3)

위험 및 안전 성명

위험품 표기	Xi
위험 카페고리 넘버	36/37/38
안전지침서	26-36
유엔번호(UN No.)	UN 3082 9 / PGIII
WGK 독일	2
RTECS 번호	DH2207000
독성	Both the acute oral LD₅₀ value in rats and the acute dermal LD₅₀ value in rabbits exceeded 5 g/kg (Moreno, 1975).

그림문자(GHS)

헥실살리실레이트 화학적 특성, 용도, 생산

화학적 성질
Hexyl Salicylate has been reported in carnation flower absolute . It is a colorless liquid with a green, floral, spicy odor, reminiscent of azaleas. It is used for blossom and herbal notes in perfumes, for example, in soaps, personal hygiene products, and detergents.
출처
Has apparently not been reported to occur in nature.
용도
Hexyl salicylate may be used as an internal standard for the determination of allergenic ester, benzyl salicylate in propolis specimens using gas chromatography-mass spectrometry (GC?MS), high-performance liquid chromatography (HPLC), and ultraviolet-visible (UV?Vis) spectrophotometry. It may also be used as a standard fragrance material for the quantification of the analyte in wastewater treatment plants using gas chromatography-mass spectrometry (GC?MS).
제조 방법
By methyl salicylate exchange with n-hexanol using a sodium methoxylate catalyst.
일반 설명
Hexyl salicylate belongs to the class of flavor & fragrance standards, for use in food, beverage and cosmetic industry. These standards are widely used to add taste and/or smell to products without aroma, to mask unpleasant odors and to maintain stability of original flavor.
신진 대사
Because of the widespread medicinal use of salicyclic acid and its derivatives, there is an extensive literature on the metabolism and excretion of these compounds. Most esters of salicyclic acid hydrolyse to salicylic acid in the body, but this occurs more readily with the lower esters, little of the amyl ester being split. A large proportion of salicylic acid is excreted unchanged by most species; salicyluric acid, gentisic acid, and salicylglucuronides are also known to be excreted (Williams. 1959). Salicylic acid has been found to be teratogenic to rats (Koshakji. 1972).

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