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triclocarban

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Feature Good stability
Classification Paint Additives
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C13H9Cl3N2O

101-20-2

Uses

Personal care, such as antimicrobial soap, cosmetics, mouthwash, personal care products formulated with a recommended concentration of 0.2% to 0.5%

Pharmaceutical and industrial materials, antibacterial detergents, wound or medical disinfectants and antibacterial textile finishes

Names and Identifiers

Name3,4,4′-trichlorocarbanilide
SynonymsTCC
3,4,4
Procutene
solubacter
TRICLOCARBAN
TRICHLOROCARBANILIDE
3,4,4′-trichlorocarbanilide
3,4,4′-trichloro-carbanilid
Carbanilide, 3,4,4′-trichloro-
3,4,4′- Trichloro-sym-diphenylurea
1-(3,4-dichlorophenyl)-3-phenylurea
1-(4-chlorophenyl)-3-(3,4-dichlorophenyl)urea
N-(3,4-DICHLOROPHENYL)-N’-(4-CHLOROPHENYL)UREA
N-(4-CHLOROPHENYL)-N-(3,4-DICHLOROPHENYL)-UREA
CAS101-20-2
EINECS202-924-1
InChIInChI=1/C13H10Cl2N2O/c14-11-7-6-10(8-12(11)15)17-13(18)16-9-4-2-1-3-5-9/h1-8H,(H2,16,17,18)
InChIKeyICUTUKXCWQYESQ-UHFFFAOYSA-N

101-20-2 – Physico-chemical Properties

Molecular FormulaC13H9Cl3N2O
Molar Mass315.58
Density1.5732 (rough estimate)
Melting Point254-256 °C (lit.)
Boling Point344.2±42.0 °C(Predicted)
Flash Point150°C
SolubilitySoluble in methanol
Vapor Presure<0.1 mm Hg ( 25 °C)
AppearanceWhite fine powder
ColorFine plates
Merck14,9654
pKa12.77±0.70(Predicted)
Storage ConditionSealed in dry,Room Temperature
StabilityStable. Combustible. Incompatible with strong oxidizing agents strong bases.
Refractive Index1.6300 (estimate)
MDLMFCD00013254
Physical and Chemical PropertiesWhite powder.
In vitro studyTriclocarban (300 nM) potentiates the cytotoxicity of 300 µM H 2 O 2 in rat thymocytes. Triclocarban (300 nM) does not increase the population of death cells, it facilitates the process of cell death induced by H 2 O 2 , resulting in further increase in the population of dead cells. Triclocarban exertes estrogenic activities by inducing luciferase activities in an ER reporter gene assay, promoting the proliferation of the MCF-7 cells, up-regulating the expression of pS2 and down-regulating ERα expression at both the mRNA and protein levels in the MCF-7 cells.
In vivo studyTriclocarban is absorbed significantly from soap used during showering in human subjects and that its C max in their whole blood ranges from 23 nM to 530 nM. Gestational triclocarban exposure does not affect the ability of dams to carry offspring to term but triclocarban exposure during lactation has adverse consequences on the survival of offspring.

101-20-2 – Risk and Safety

Hazard SymbolsN – Dangerous for the environment
Risk Codes50/53 – Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment.
Safety DescriptionS60 – This material and its container must be disposed of as hazardous waste.
S61 – Avoid release to the environment. Refer to special instructions / safety data sheets.
UN IDsUN 3077 9/PG 3
WGK Germany2
RTECSFE1250000
HS Code38220090
Hazard Class9
Packing GroupIII
ToxicityLD50 ipr-mus: 2100 mg/kg LPPTAK 27,306,79

Reference Information

LogP    3.633 at 25℃
Use      triclocarban is used as a bacteriostatic agent and preservative in soap and other cleaning compositions. Preservatives, disinfectants.
daily chemical bacteriostatic agent. It has the characteristics of continuous, safe and stable sterilization, has excellent compatibility with skin, and has high-efficiency inhibitory effect on gram-positive bacteria, gram-negative bacteria, fungi, yeasts and viruses.
It has antibacterial effect and is widely used in washing powder, soap, shower gel, etc.

biological activity    Triclocarban is an anti-bacterial agent commonly used in personal care products.

target    Bacterial

Declaration: The products displayed on this website are intended exclusively for industrial applications or scientific research. They are not intended for medical, pharmaceutical, or food use. In accordance with applicable laws and regulations, purchasing organizations must hold valid qualifications and approvals.

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