트란스-아니솔

트란스-아니솔
트란스-아니솔 구조식 이미지
카스 번호:
4180-23-8
한글명:
트란스-아니솔
동의어(한글):
트란스-아니솔;트랜스-아네톨
상품명:
trans-Anethole
동의어(영문):
ANETHOLE;trans-Anethol;(E)-anethole;(E)-1-Methoxy-4-(prop-1-en-1-yl)benzene;P-PROPENYLANISOLE;4-trans-propenyl-anisole;FEMA 2086;PARA METHOXY ALPHA PHENYL PROPENE;ANETHOLUM;1-METHOXY-4-PROPENYLBENZENE
CBNumber:
CB3228733
분자식:
C10H12O
포뮬러 무게:
148.2
MOL 파일:
4180-23-8.mol
MSDS 파일:
SDS

트란스-아니솔 속성

녹는점
20-21 °C(lit.)
끓는 점
234-237 °C(lit.)
밀도
0.988 g/mL at 25 °C(lit.)
증기압
1.33 hPa (63 °C)
FEMA
2086 | TRANS-ANETHOLE
굴절률
n20/D 1.561(lit.)
인화점
195 °F
저장 조건
2-8°C
용해도
벤젠, 에틸 아세테이트, 아세톤, 이황화탄소에 용해됩니다.
물리적 상태
녹은 후에 액체
색상
무색~담황색 투명
수소이온지수(pH)
7 (H2O)
냄새
디프로필렌 글리콜 중 10.00%. 달콤한 아니스 감초 미모사
?? ??
감초
수용성
실질적으로 불용성
감도
Light Sensitive
Merck
14,643
JECFA Number
217
BRN
774229
안정성
감광성
InChIKey
RUVINXPYWBROJD-ONEGZZNKSA-N
LogP
3.388
CAS 데이터베이스
4180-23-8(CAS DataBase Reference)
NIST
Anethole(4180-23-8)
EPA
(E)-Anethole (4180-23-8)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi,N
위험 카페고리 넘버 43-51/53
안전지침서 36/37-61
유엔번호(UN No.) UN 3077 9 / PGIII
WGK 독일 2
RTECS 번호 BZ9275000
F 고인화성물질 8
TSCA Yes
HS 번호 29093090
독성 LD50 orally in Rabbit: 2090 mg/kg LD50 dermal Rabbit > 5000 mg/kg
기존화학 물질 KE-05-0140
그림문자(GHS): GHS hazard pictogramsGHS hazard pictograms
신호 어: Warning
유해·위험 문구:
암호 유해·위험 문구 위험 등급 범주 신호 어 그림 문자 P- 코드
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
H411 장기적 영향에 의해 수생생물에 유독함 수생 환경유해성 물질 - 만성 구분 2
예방조치문구:
P261 분진·흄·가스·미스트·증기·...·스프레이의 흡입을 피하시오.
P272 작업장 밖으로 오염된 의복을 반출하지 마시오.
P273 환경으로 배출하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
P333+P313 피부자극성 또는 홍반이 나타나면 의학적인 조치·조언를 구하시오.
NFPA 704
1
1 0

트란스-아니솔 MSDS


1-Methoxy-4-((E)-propenyl)-benzene

트란스-아니솔 C화학적 특성, 용도, 생산

개요

(E)-Anethol is a phenylpropanoid that has been found in P. anisum seed oil and has antifungal and antioxidant activity. It is active against fermentatively growing S. cerevisiae under hypoxic, but not normoxic, conditions (MIC = 100 μg/ml), and against C. parapsilosis when used at a concentration of 15% w/w. (E)-Anethol has antioxidant activity in a Trolox equivalent antioxidant capacity (TEAC) assay but does not scavenge 2,2-diphenyl-1-picrylhydrazel (DPPH) radicals in a cell-free assay.

화학적 성질

trans-anethole is a clear colorless to pale yellow liquid and has a characteristic anise, sweet, spicy, warm odor and corresponding sweet taste.
Anethole
Anethole (1-methoxy-4-propenyl-benzene, isoestragole) is an alkoxypropenylbenzene derivative and an important favoring component of essential oils of more than 20 plant species. Essential oils from seeds of anise (Pimpinellaanisum L.), star anise (Illicium verum Hook.f), and sweet fennel (Foeniculum vulgare Mill. var. dulce) are the main sources used for the isolation of anethole. Two isomers of anethole occur in nature: E- or trans-anethole and Z-or cis-anethole. About 90 % of natural anethole is trans-isomer. Besides separation from natural essential oils, anethole is obtained using the rectification of crude sulfate turpentine and/or the organic synthesis starting from methylchavicol or anisole and propionic anhydride. Compared to natural compound, synthetic trans-anethole is impurified with higher amounts of cis-isomer.

출처

Anethole is methyl ether of oestrone and has been found in fennel, aniseed, coriander, and many other volatile oils.

용도

trans-Anethole is used to inhibits lung and forestomach carcinogenesis, used as carbon and energy supplement in the culture media of Pseudomonas putida strain. It is also used as used as a flavoring substance.

제조 방법

By esterification of p-cresol with methyl alcohol and with subsequent condensation with α-cetaldehyde (Perknis); the most common method of preparation is from pine oil. By fractional distillation of the essential oils of anise, star anise, and fennel; the anise essences contain an average of 85% anethole; fennel, from 60 to 70%.

일반 설명

trans-Anethole is a naturally occuring flavouring agent. It has insecticidal, larvicidal, and antimicrobial properties.

Anticancer Research

It is one of the major constituents of essential oil of fennel and anise and belongs tothe class of phenylpropenes. It has the capacity to block both inflammation andcarcinogenesis. It is an antioxidant and also a suppressor of NF-κB activation byIκBα degradation (Aggarwal and Shishodia 2004).

신진 대사

Anethole is metabolized by oxidation of the propenyl group and is excreted as anisic acid (Williams, 1959). The metabolism of trans-anethole used in the preparation of anis-flavoured alcoholic beverages was studied in the rabbit and rat after iv and oral administration. It was excreted rapidly from the animal regardless of the method of administration. After iv injection it was found concentrated in the liver, lungs and brain; after oral administration, absorption was slight and most of it remained in the stomach. Ethyl alcohol has no effect on the metabolism (Le Bourhis, 1968).

트란스-아니솔 준비 용품 및 원자재

원자재

준비 용품


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