아니졸

아니졸
아니졸 구조식 이미지
카스 번호:
100-66-3
한글명:
아니졸
동의어(한글):
아니솔;아니졸
상품명:
Anisole
동의어(영문):
METHOXYBENZENE;ANISOL;MOB;METHYL PHENYL ETHER;Anizol;ANISLOE;ANISOLE;Amisale;FEMA 2097;7) ANISOLE
CBNumber:
CB5100716
분자식:
C7H8O
포뮬러 무게:
108.14
MOL 파일:
100-66-3.mol
MSDS 파일:
SDS

아니졸 속성

녹는점
-37 °C (lit.)
끓는 점
154 °C (lit.)
밀도
0.995 g/mL at 25 °C (lit.)
증기 밀도
3.7 (vs air)
증기압
10 mm Hg ( 42.2 °C)
FEMA
2097 | ANISOLE
굴절률
n20/D 1.516(lit.)
인화점
125 °F
저장 조건
Store below +30°C.
용해도
1.71g/L
물리적 상태
액체
색상
무색의
상대극성
0.198
냄새
페놀, 아니스 냄새
Odor Threshold
0.057ppm
폭발한계
0.34-6.3%(V)
?? ??
페놀성
수용성
1.6g/L(20℃)
Merck
14,669
JECFA Number
1241
BRN
506892
Dielectric constant
4.3(20℃)
안정성
안정적인. 가연성. 강한 산화제와 호환되지 않습니다.
InChIKey
RDOXTESZEPMUJZ-UHFFFAOYSA-N
LogP
2.62 at 30℃
CAS 데이터베이스
100-66-3(CAS DataBase Reference)
NIST
Benzene, methoxy-(100-66-3)
EPA
Anisole (100-66-3)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xn,Xi
위험 카페고리 넘버 10-38-20-36/37
안전지침서 37/39-26-16-24/25
유엔번호(UN No.) UN 2222 3/PG 3
WGK 독일 2
RTECS 번호 BZ8050000
자연 발화 온도 887 °F
TSCA Yes
위험 등급 3
포장분류 III
HS 번호 29093090
유해 물질 데이터 100-66-3(Hazardous Substances Data)
독성 LD50 orally in rats: 3700 mg/kg (Taylor)
기존화학 물질 KE-23213
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
H226 인화성 액체 및 증기 인화성 액체 구분 3 경고
H336 졸음 또는 현기증을 일으킬 수 있음 특정표적장기 독성 물질(1회 노출);마취작용 구분 3 경고 P261, P271, P304+P340, P312,P403+P233, P405, P501
예방조치문구:
P210 열·스파크·화염·고열로부터 멀리하시오 - 금연 하시오.
P233 용기를 단단히 밀폐하시오. 용기는 환기가 잘 되는 곳에 단단히 밀폐하여 보관하시오.
P240 용기와 수용설비를 접지 및 접합시키시오.
P241 폭발 방지용 장비[전기적/환기/조명/...]을(를) 사용하시오.
P242 스파크가 발생하지 않는 도구를 사용하시오
P243 정전기 방지 조치를 취하시오.
NFPA 704
2
1 0

아니졸 C화학적 특성, 용도, 생산

개요

Anisole is a colorless liquid with a spicy-sweet smell. Anisole can be produced by all the aforementioned methods. It is an important intermediate in the synthesis of organic compounds, for example fragrances and pharmaceuticals. The compound is also used as a solvent and as a heat transfer medium.

화학적 성질

Anisole is a colorless to yellowish liquid with a characteristic pleasant, anise-like, agreeable, aromatic, spicy-sweet odor. It is used in perfumery.

출처

Anisole is a natural product found in apple juice and in the oil of Artemisia dracunculus var. turkestanica; also reported found in butter, Camembert cheese, roasted beef, olive (Olea europae), Malay apple, Jerusalem artichoke (Helianthus tuberosus), Bourbon vanilla, truffles, crab and sopadilla fruit (Achras sapota L.).

용도

Anisole is widely used as a solvent for the synthesis of various organic compounds, anethole, nonylphenol isomer 4-(3',6'-dimethyl-3-heptyl)phenol, perfumes, insect pheromones and pharmaceuticals. It finds application in the preparation of inorganic complexes and materials such as tin-core/tin oxide nanoparticles.

주요 응용

Anisole is an organic compound with the chemical formula C7H8O with a pleasant anise-like aroma, used in organic synthesis and also as a solvent, fragrance and insect repellent. For organic synthesis, it is also used as solvent, fragrance and insect repellent.

제조 방법

Anisole is synthesized by reacting phenol and dimethyl sulfate in the presence of aqueous NaOH; by passing methyl chloride into a suspension of sodium phenolate in liquid ammonia.

정의

ChEBI: Anisole is a monomethoxybenzene that is benzene substituted by a methoxy group. It has a role as a plant metabolite.

일반 설명

A clear straw-colored liquid with an aromatic odor. Insoluble in water and the same density as water. Vapors heavier than air. Flash point 125°F. Boiling point 307°F. Moderately toxic by ingestion. A skin irritant. Used to make perfumes, flavorings and as a solvent.

공기와 물의 반응

Flammable. Ethers tend to form unstable peroxides when exposed to oxygen. Ethyl, isobutyl, ethyl tert-butyl, and ethyl tert-pentyl ether are particularly hazardous in this respect. Ether peroxides can sometimes be observed as clear crystals deposited on containers or along the surface of the liquid. Insoluble in water

반응 프로필

Ethers, such as Anisole can act as bases. They form salts with strong acids and addition complexes with Lewis acids. The complex between diethyl ether and boron trifluoride is an example. Ethers may react violently with strong oxidizing agents. In other reactions, which typically involve the breaking of the carbon-oxygen bond, ethers are relatively inert.

건강위험

Inhalation or contact with material may irritate or burn skin and eyes. Fire may produce irritating, corrosive and/or toxic gases. Vapors may cause dizziness or suffocation. Runoff from fire control or dilution water may cause pollution.

Safety Profile

Moderately toxic by ingestion and inhalation. A skin irritant. A flammable liquid. To fight fire, use foam, CO2, dry chemical. When heated to decomposition it emits acrid fumes.

잠재적 노출

Anisole is used as a solvent; a flavoring, vermicide, making perfumes; and in organic synthesis.

Purification Methods

Shake anisole with half its volume of 2M NaOH, and the emulsion is allowed to separate. Repeat three times, then wash twice with water, dry over CaCl2, filter, dry over sodium wire and finally distil it from fresh sodium under N2 using a Dean-Stark trap (samples in the trap being rejected until free from turbidity) [Caldin et al. J Chem Soc, Faraday Trans 1 72 1856 1976]. Alternatively dry it with CaSO4 or CaCl2, or by refluxing with sodium or BaO with crystalline FeSO4 or by passage through an alumina column. Traces of phenols are removed by prior shaking with 2M NaOH, followed by washing with water. It has been be purified by zone refining. [Beilstein 6 IV 548.]

비 호환성

Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides.

폐기물 처리

Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.

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