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N,N''-Bis(4-chlorphenyl)-3,12-diimino-2,4,11,13-tetraazatetrade-candiimidamid

Chlorhexidine

HCID 5353524
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Grundinformationen

CAS
55-56-1
Standard-SMILES
NC(=NCCCCCCN=C(N)/N=C(/N)Nc1ccc(Cl)cc1)/N=C(/N)Nc1ccc(Cl)cc1
InChIKey
GHXZTYHSJHQHIJ-UHFFFAOYSA-N
Summenformel
C22H30Cl2N10
Durchschnittliche Molmasse
505,45 g/mol

Namen und Bezeichner

Bevorzugter Name
Chlorhexidine
Lokaler Name
N,N''-Bis(4-chlorphenyl)-3,12-diimino-2,4,11,13-tetraazatetrade-candiimidamid
Englischer Name
Chlorhexidine
Summenformel
C22H30Cl2N10
Molmasse
505.45

Namen und Synonyme

CHLORHEXIDINE BASECHLOROHEXIDINEchlorhexidinsterilonfimeilhexadolsoretolnolvasanrotersepttubulicid

Datenbank-Bezeichner

CAS
55-56-1
PubChem CID
5353524

Eigenschaften

Physikochemische Eigenschaften

Schmelzpunkt
134 · 134-136 °C (lit.)
Siedepunkt
641.45 °C · 641.45°C (rough estimate)
Dichte
1.1555 · 1.1555 (rough estimate)
Brechungsindex
1.63 · 1.6300 (estimate)
storage temp.
2 · 2-8°C
Löslichkeit
0.08 % · water: soluble0.08% at 20°C
Aggregatzustand
Solid
pka
10.78 · pKa 10.78 (Uncertain)
Farbe
White to off-white
Wasserlöslichkeit
0.08 g/100 · 0.08 g/100 mL (20 ºC)
Merck
13 · 13,2108
BRN
2826432 · 2826432
Henry's Law Constant
9 · 9.0×1024 mol/(m3Pa) at 25℃, HSDB (2015)
Stabilität
Stable. Incompatible with strong oxidizing agents.
Kosmetik-Inhaltsstoffe Funktionen
PRESERVATIVEORAL CAREANTIMICROBIAL
InChIKey
GHXZTYHSJHQHIJ-UHFFFAOYSA-N
SMILES
Clc1ccc(NC(=N)NC(=N)NCCCCCCNC(=N)NC(=N)Nc2ccc(Cl)cc2)cc1
LogP
0.08 · 0.080
CAS Datenbank
55 · 55-56-1(CAS DataBase Reference)
EPA chemische Informationen
Chlorhexidine (55-56-1)

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

Sicherheitsdaten

F
10-34
wgk
3
tsca
TSCA listed
ridadr
UN 3077 9/PG 3
hs_code
29215900
RTECS-Nr.
DU1925000
risk_code
36/37/38-43-51/53-50/53
Toxizität
LD50 orally in Rabbit: 5000 mg/kg
hazard_code
Xi,N
safety_code
26-36/37-60-61
hazard_class
9
packing_group
III
Speicherklasse
11 - Combustible Solids
Giftige Stoffe Daten
55-56-1(Hazardous Substances Data)
Hazard Classifications
Aquatic Acute 1Aquatic Chronic 1Eye Dam. 1

Chemie und Industrie

Anwendungen · 2 Einträge

BeschreibungChlorhexidine 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.

VerwendenChlorhexidine 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.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

4-ChloraniliniumchloridHexamethylendiammoniumdichlorid

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Ergänzende Hinweise

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