트리클로산

트리클로산
트리클로산 구조식 이미지
카스 번호:
3380-34-5
한글명:
트리클로산
동의어(한글):
트라이클로산;트리클로산;2,4,4'-트라이클로로-2'-하이드록시다이페닐 에터;2,4,4'-트라이클로로-2'-하이드록시다이페닐에터;2'-하이드록시-2,4,4'-트라이클로로다이페닐 에터;3-클로로-6-(2,4-다이클로로페녹시)페놀;4-클로로-2-하이드록시페닐 2,4-다이클로로페닐 에터;5-클로로-2-(2',4'-다이클로로페녹시)페놀;5-클로로-2-(2,4-다이클로로페녹시)페놀
상품명:
Triclosan
동의어(영문):
IRGASAN;ch3565;TROX-100;riclosan;TRICLOSAN;Yriclosan;TRICHLOSAN;Cloxifenol;ZilesanUW.;Ttriclosan
CBNumber:
CB6771432
분자식:
C12H7Cl3O2
포뮬러 무게:
289.54
MOL 파일:
3380-34-5.mol
MSDS 파일:
SDS

트리클로산 속성

녹는점
56-60 °C(lit.)
끓는 점
290°C(lit.)
밀도
1.4214 (rough estimate)
증기압
0.001Pa at 25℃
굴절률
1.4521 (estimate)
저장 조건
2-8°C
용해도
H2O: 20°C에서 용해성12g/L
산도 계수 (pKa)
7.9(at 25℃)
물리적 상태
고체
물리적 상태
단단한 모양
색상
무색 또는 흰색
수용성
에탄올, 메탄올, 디에틸 에테르 및 수산화나트륨 용액(1M)에 용해됩니다. 물에 약간 용해됩니다.
Merck
14,9657
BRN
2057142
안정성
안정적인. 강한 산화제와 호환되지 않습니다.
InChIKey
XEFQLINVKFYRCS-UHFFFAOYSA-N
LogP
4.9 at 20℃
CAS 데이터베이스
3380-34-5(CAS DataBase Reference)
NIST
Triclosan(3380-34-5)
EPA
Triclosan (3380-34-5)
안전
  • 위험 및 안전 성명
  • 위험 및 사전주의 사항 (GHS)
위험품 표기 Xi,N
위험 카페고리 넘버 36/38-50/53-36/37/38
안전지침서 26-39-46-60-61-24/25-22-36
유엔번호(UN No.) UN 3077 9/PG 3
WGK 독일 2
RTECS 번호 KO1100000
TSCA Yes
위험 등급 9
포장분류 III
HS 번호 29095000
유해 물질 데이터 3380-34-5(Hazardous Substances Data)
독성 LD50 orl-rat: 3700 mg/kg 26UZAB 6,245,68/70
기존화학 물질 KE-05588
유해화학물질 필터링 2009-1-599
함량 및 규제정보 물질구분: 유독물질; 혼합물(제품)함량정보: 트리클로산 및 이를 25% 이상 함유한 혼합물
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
H315 피부에 자극을 일으킴 피부부식성 또는 자극성물질 구분 2 경고 GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 눈에 심한 자극을 일으킴 심한 눈 손상 또는 자극성 물질 구분 2A 경고 GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H410 장기적 영향에 의해 수생생물에 매우 유독함 수생 환경유해성 물질 - 만성 구분 1 경고 GHS hazard pictograms P273, P391, P501
예방조치문구:
P264 취급 후에는 손을 철저히 씻으시오.
P264 취급 후에는 손을 철저히 씻으시오.
P273 환경으로 배출하지 마시오.
P280 보호장갑/보호의/보안경/안면보호구를 착용하시오.
P302+P352 피부에 묻으면 다량의 물로 씻으시오.
P305+P351+P338 눈에 묻으면 몇 분간 물로 조심해서 씻으시오. 가능하면 콘택트렌즈를 제거하시오. 계속 씻으시오.
P332+P313 피부 자극이 생기면 의학적인 조치· 조언을 구하시오.
NFPA 704
1
2 0

트리클로산 C화학적 특성, 용도, 생산

개요

Triclosan is a broad-spectrum antibacterial agent that inhibits bacterial fatty acid synthesis. It is effective against Gram-negative and Gram-positive bacteria, as well as against Mycobacteria. Triclosan is used in a variety of products, including antiseptic soaps, deodorants, and hand washes.

화학적 성질

Solid

용도

triclosan is a preservative considered to have a low sensitizing potential in leave-on preparations.

정의

ChEBI: An aromatic ether that is phenol which is substituted at C-5 by a chloro group and at C-2 by a 2,4-dichlorophenoxy group. It is widely used as a preservative and antimicrobial agent in personal care products such as soaps, skin creams, toothpaste and deodo ants as well as in household items such as plastic chopping boards, sports equipment and shoes.

Indications

Triclosan is a broad-spectrum antimicrobial compound. It was originally used in soaps, antiperspirants, and cosmetic toiletries as a germicide. Today, triclosan is incorporated into toothpaste because of its wide spectrum of antimicrobial activities and low toxicity.

일반 설명

Chemical structure: diphenyl ether derivative

Mechanism of action

Triclosan is active against a broad range of oral grampositive and gram-negative bacteria.The primary target of its antibacterial activity is the bacterial cell membrane. High concentrations cause membrane leakage and ultimately lysis of the bacterial cell. Effects at lower concentration are more subtle. Triclosan has been shown to bind to cell membrane targets and inhibit enzymes associated with the phosphotransferase and proton motive force systems.

Pharmacology

Triclosan is retained in dental plaque for at least 8 hours, which in addition to its broad antibacterial property could make it suitable for use as an antiplaque agent in oral care preparations. However, the compound is rapidly released from oral tissues, resulting in relatively poor antiplaque properties as assessed in clinical studies of plaque formation.This observation is further corroborated by a poor correlation between minimal inhibitory concentration values generated in vitro and clinical plaque inhibitory properties of triclosan. Improvement of substantivity was accomplished by incorporation of triclosan in a polyvinyl methyl ether maleic acid copolymer (PVM/MA, Gantrez). With the combination of PVM/MA copolymer and triclosan, the substantivity of the triclosan was increased to 12 hours in the oral cavity.

Clinical Use

Triclosan plus copolymer is available in toothpaste. Commercially available dentifrice concentrations contain 0.3% triclosan and 2.0% PVM/MA copolymer.

부작용

Triclosan is a preservative used in health care and consumer products, including soaps, deodorants, mouthwashes, toothpastes, cosmetics, and topical medicaments. Ozkaya et al. described a case of suspected immune mediated Cou to triclosan. A 44-year-old female reported experiencing an immediate localized urticarial response after contact with numerous topical products. The use of a toothpaste had also resulted in swelling of her lips, tongue, and breathing difficulties. She also experienced lip swelling after kissing her husband who had used the same product and wheals involving her face after kissing friends on the cheek who had used certain topical products on their faces. The suspected products all contained triclosan 0.2%–0.5%. A severe localized urticarial reaction occurred with open testing to 2% triclosan within 15 minutes. No tests were performed to confirm an immunological mechanism; however, the authors suspected this to be the case because of a positive urticarial response to triclosan within 15 minutes, a history of angioedema to the triclosan-containing toothpaste, and because no immediate reactions were seen in five control subjects who were open tested to 2% triclosan.

Safety Profile

Poison by intravenous andintraperitoneal routes. Moderately toxic by ingestion.Mildly toxic by skin contact. Mutation data reported. Ahuman skin irritant. When heated to decomposition itemits toxic fumes of Clí.

트리클로산 준비 용품 및 원자재

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