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클로르헥시딘

Chlorhexidine

HCID 9552079
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기본 정보이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
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기본 정보

CAS
55-56-1
표준 SMILES
NC(=NCCCCCCN=C(N)/N=C(\N)Nc1ccc(Cl)cc1)/N=C(\N)Nc1ccc(Cl)cc1
InChIKey
GHXZTYHSJHQHIJ-UHFFFAOYSA-N
분자식
C22H30Cl2N10
평균 분자량
505.45 g/mol

이름 및 식별자

우선 이름
Chlorhexidine
현지명
클로르헥시딘
영어명
Chlorhexidine
분자식
C22H30Cl2N10
분자량
505.45

이름 및 동의어

클로르헥시딘클로헥시딘CHLORHEXIDINE BASECHLOROHEXIDINEchlorhexidinsterilonfimeilhexadolsoretolnolvasanrotersepttubulicid

데이터베이스 식별자

CAS
55-56-1
PubChem CID
9552079
ChEMBL
CHEMBL790
ChEBI
CHEBI:3614
UNII
R4KO0DY52L
EC Number
200-238-7
Nikkaji
J4.561F

물성

물리화학적 성질

녹는점
134 · 134-136 °C (lit.)
끓는 점
641.45 °C · 641.45°C (rough estimate)
밀도
1.1555 · 1.1555 (rough estimate)
굴절률
1.63 · 1.6300 (estimate)
저장 조건
2 · 2-8°C
용해도
20 °C에서 · 물: 20°C에서 용해성0.08%
물리적 상태
Solid
산도 계수 (pKa)
10.78 · pKa 10.78 (Uncertain)
색상
White to off-white
수용성
0.08 g/100mL · 0.08g/100mL(20℃)
Merck
13 · 13,2108
BRN
2826432 · 2826432
Henry's Law Constant
9 · 9.0×1024 mol/(m3Pa) at 25℃, HSDB (2015)
안정성
안정적인. 강한 산화제와 호환되지 않습니다.
화장품 원료 기능
항균 방부제구강 관리항균
InChIKey
GHXZTYHSJHQHIJ-UHFFFAOYSA-N
SMILES
Clc1ccc(NC(=N)NC(=N)NCCCCCCNC(=N)NC(=N)Nc2ccc(Cl)cc2)cc1
LogP
0.08 · 0.080
EPA
Chlorhexidine (55-56-1)

화학적 성질

Chlorhexidine occurs as an odorless, bitter tasting, white crystalline powder.

안전 및 규제

안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.

안전 데이터

wgk
3
tsca
TSCA listed
rtecs
DU1925000
ridadr
UN 3077 9/PG 3
독성
LD50 orally in Rabbit: 5000 mg/kg
HS 번호
29215900
risk_code
36/37/38-43-51/53-50/53
hazard_code
Xi,N
safety_code
26-36/37-60-61
포장분류
III
위험 등급
9
F 고인화성물질
10-34
Hazard Classifications
Aquatic Acute 1Aquatic Chronic 1Eye Dam. 1
스토리지 클래스
11 - Combustible Solids
유해 물질 데이터
55-56-1(Hazardous Substances Data)

화학 및 산업

응용 분야 · 3건

개요Chlorhexidine is a cationic broad-spectrum antimicrobial agent belonging to the bis(biguanide) family. Its mechanism of action involves destabilization of the outer bacterial membrane. It is effective on both Gram-positive and Gram-negative bacteria, although it is less effective with some Gram-negative bacteria. It has both bactericidal and bacteriostatic mechanisms of action. Chlorhexidine's antimicrobial effects are associated with the attractions between chlorhexidine (cation) and negatively charged bacterial cells. After chlorhexidine is absorpted onto the organism's cell wall, it disrupts the integrity of the cell membrane and causes the leakage of intracellular components of the organisms. Aqueous solutions of chlorhexidine are most stable within the pH range of 5-8. Above pH 8.0 chlorhexidine base is precipitated and in more acid conditions there is gradual deterioration of activity because the compound is less stable. Chlorhexidine is used primarily as a topical antiseptic/disinfectant in wound healing, at catheterization sites, in various dental applications and in surgical scrubs. It has a LD-50 orally in mice as a diacetate at 2gm./kg. In digluconate form the LD-50 is 1800 gm./kg.

용도Chlorhexidine is an antibacterial used for numerous applications. It is a cationic polybiguanide (bisbiguanide) used primarily as its salts, dihydrochloride, diacetate, and digluconate. Chlorhexidine is one of those drugs which are enlisted/included in the World Health Organization's List of Essential Medicines, a list of the most important drugs needed in a basic health system. Chlorhexidine is used as a germicidal compound in teat dips. Also used as navel treatment, udder and eye wash, surgical scrub and sterilization material. Chlorhexidine is used primarily as a topical antiseptic/disinfectant in wound healing, at catheterization sites, in various dental applications and in surgical scrubs. it is used as an antibacterial agent in humans to control gingivitis and over all plaque control in preventative dentistry. Hydrogenolysis of benzyl-nitrogen bonds. Bacteriostatic;Detergent.

일반 설명Effect of the chlorhexidine:hydroxypropyl-β-cyclodextrin inclusion compound on in vitro slabs of bovine dentine has been investigated.

제조 방법 · 1건

생산 방법Chlorhexidine may be prepared either by condensation of polymethylene bisdicyandiamide with 4-chloroaniline hydrochloride or by condensation of 4-chlorophenyl dicyandiamine with hexamethylenediamine dihydrochloride. Chlorhexidine may also be synthesized from a series of biguanides.

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상·하류 제품 정보

상류 원료

4-Chlorobenzenamine hydrochloride헥사메틸렌디아민 디염화수소산염

추가 설명

정의ChEBI: A bisbiguanide compound with a structure consisting of two (p-chlorophenyl)guanide units linked by a hexamethylene bridge.