시클라멘 알데히드

시클라멘 알데히드
시클라멘 알데히드 구조식 이미지
카스 번호:
103-95-7
한글명:
시클라멘 알데히드
동의어(한글):
시클라멘알데히드;사이클라멘알데하이드
상품명:
cyclamen aldehyde
동의어(영문):
3-(4-Isopropylphenyl)-2-methylpropanal;Cyclamal;2-METHYL-3-(P-ISOPROPYLPHENYL)PROPIONALDEHYDE;3-p-cumenyl-2-methylpropionaldehyde;3-(4-ISOPROPYLPHENYL)ISOBUTYRALDEHYDE;3-(4-ISOPROPYLPHENYL)-2-METHYLPROPIONALDEHYDE;(R,S)-p-Isopropyl-α-methylhydro-cinnamaldehyde;3-p-;FEMA 2743;aldehydeb
CBNumber:
CB9246702
분자식:
C13H18O
포뮬러 무게:
190.28
MOL 파일:
103-95-7.mol
MSDS 파일:
SDS

시클라멘 알데히드 속성

끓는 점
270 °C(lit.)
밀도
0.95 g/mL at 25 °C(lit.)
증기압
0.3Pa at 20℃
FEMA
2743 | 2-METHYL-3-(P-ISOPROPYLPHENYL)PROPIONALDEHYDE
굴절률
n20/D 1.505(lit.)
인화점
228 °F
저장 조건
Inert atmosphere,Room Temperature
용해도
클로로포름(약간 용해됨), 에틸아세테이트, 메탄올(약간 용해됨)
물리적 상태
기름
색상
무색 액체.
냄새
플로럴 타입에 사용되는 독특한 오이-멜론 향을 지닌 강력한 플로럴 그린입니다.
?? ??
꽃향기
수용성
66mg/L at 20℃
JECFA Number
1465
안정성
흡습성
LogP
3.4 at 35℃
CAS 데이터베이스
103-95-7(CAS DataBase Reference)
EPA
Benzenepropanal, .alpha.-methyl-4-(1-methylethyl)- (103-95-7)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi
위험 카페고리 넘버 38
안전지침서 26-36
WGK 독일 2
RTECS 번호 MW4900000
HS 번호 29122990
독성 The acute oral LD50 value in rats was reported as 3*81 g/kg (Jenner, Hagan, Taylor, Cook & Fitzhugh, 1964).
기존화학 물질 KE-24403
그림문자(GHS): GHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
H315 피부에 자극을 일으킴 피부부식성 또는 자극성물질 구분 2 경고 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H317 알레르기성 피부 반응을 일으킬 수 있음 피부 과민성 물질 구분 1 경고 GHS hazard pictograms P261, P272, P280, P302+P352,P333+P313, P321, P363, P501
H412 장기적 영향에 의해 수생생물에 유해함 수생 환경유해성 물질 - 만성 구분 3 P273, P501
예방조치문구:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P272 작업장 밖으로 오염된 의복을 반출하지 마시오.
P273 환경으로 배출하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
NFPA 704
2
0 0

시클라멘 알데히드 C화학적 특성, 용도, 생산

개요

2-Methyl-3-(p-isopropylphenyl) propionaldehyde has a strong, flowery odor. May be prepared by condensation of cuminic aldehyde and propionaldehyde followed by hydrogenation in the presence of a catalyst.

화학적 성질

The commercially available racemate is a colorless to yellowish liquid with an intense floral odor reminiscent of Cyclamen europaeum (cyclamen, sowbread).
Production. Two main processes are used for the industrial synthesis of cyclamen aldehyde:
1) Alkaline condensation of 4-isopropylbenzaldehyde and propanal results, via the aldol, in the formation of 2-methyl-3-(4-isopropylphenyl)-2-propenal. The unsaturated aldehyde is hydrogenated selectively to the saturated aldehyde in the presence of potassium acetate and a suitable catalyst, such as palladium–alumina:
2) Friedel–Crafts reaction of isopropylbenzene and 2-methylpropenal diacetate (methacrolein diacetate) in the presence of titanium tetrachloride/boron trifluoride etherate gives cyclamen aldehyde enolacetate, which is hydrolyzed to aldehyde:
Uses. Cyclamen aldehyde is an important component for obtaining special blossomnotes in perfume compositions, particularly the cyclamen type. Because of its fresh, floral aspect, it is also used as the top note in many other blossomfragrances.

출처

Reported found in nutmeg and starfruit.

용도

Cyclamen Aldehyde is a very powerful, floral, green note used in many perfumery applications to blend into fresh, floral, green or ozonic/marine accords. It is an ingredient with growing use and importance in helping to build replacement accords for materials disappearing from the Perfumers’ palette. Cyclamen has good overall stability except in extremes of pH. It has good tenacity and substantivity and represents very good value for money in new creations.In addition to its use in numerous perfume compositions, cyclamen aldehyde is an intermediate for the preparation of fungicides and fungistatic substances.

제조 방법

By condensation of cuminic aldehyde and propionaldehyde followed by hydrogenation in the presence of a catalyst

Safety Profile

Moderately toxic by ingestion. A human skin irritant. See also ALDEHYDES. When heated to decomposition it emits acrid smoke and irritating fumes.

Synthesis

Cyclamen aldehyde is synthesized from Cuminaldehyde plus Ropionaldehyde by condensation followed by selective hydrogenation and finally dehydrogenation of the Cyclamen alcohol to aldehyde.

시클라멘 알데히드 준비 용품 및 원자재

원자재

준비 용품


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