Triclocarban

ChemicalBook > CAS DataBase List > Triclocarban

Product Name: Triclocarban
CAS No.: 101-20-2
Chemical Name: Triclocarban
Synonyms: TCC;TRICHLOROCARBANILIDE;TRICHLOCARBAN;3,4,4 TRICHLOROCARBANILIDE;cusiter;CUTISAN;CP 78416;ent26925;genoface;Nobacter
CBNumber: CB7193925
Molecular Formula: C13H9Cl3N2O
Formula Weight: 315.58
MOL File: 101-20-2.mol

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Triclocarban Property

Melting point:: 254-256 °C (lit.)
Boiling point:: 344.2±42.0 °C(Predicted)
Density: 1.5732 (rough estimate)
vapor pressure: <0.1 mm Hg ( 25 °C)
refractive index: 1.6300 (estimate)
Flash point:: 150 °C
storage temp.: Sealed in dry,Room Temperature
solubility: methanol: soluble
form: Solid
pka: 12.77±0.70(Predicted)
color: Fine plates
Water Solubility: <0.1 g/100 mL at 26 ºC
Merck: 14,9654
Stability:: Stable. Combustible. Incompatible with strong oxidizing agents strong bases.
InChIKey: ICUTUKXCWQYESQ-UHFFFAOYSA-N
LogP: 3.633 at 25℃
CAS DataBase Reference: 101-20-2(CAS DataBase Reference)
NIST Chemistry Reference: 3,4,4'-Trichloro carbanilide(101-20-2)
EPA Substance Registry System: Triclocarban (101-20-2)

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Safety

Hazard Codes: N
Risk Statements: 50/53
Safety Statements: 60-61
RIDADR: UN 3077 9/PG 3
WGK Germany: 2
RTECS: FE1250000
HazardClass: 9
PackingGroup: III
HS Code: 38220090
Hazardous Substances Data: 101-20-2(Hazardous Substances Data)
Toxicity: LD50 ipr-mus: 2100 mg/kg LPPTAK 27,306,79

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H410Very toxic to aquatic life with long lasting effects

Precautionary statements

P273Avoid release to the environment.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 105937
Product name: 3,4,4′-Trichlorocarbanilide
Purity: 99%
Packaging: 5g
Price: $23.48
Updated: 2024/03/01

Sigma-Aldrich

Product number: 105937
Product name: 3,4,4′-Trichlorocarbanilide
Purity: 99%
Packaging: 100g
Price: $98
Updated: 2024/03/01

Sigma-Aldrich

Product number: 05666
Product name: Triclocarban
Purity: analytical standard
Packaging: 25MG
Price: $84.5
Updated: 2024/03/01

TCI Chemical

Product number: T1015
Product name: 3,4,4'-Trichlorocarbanilide
Purity: >98.0%(HPLC)(N)
Packaging: 25g
Price: $48
Updated: 2024/03/01

TCI Chemical

Product number: T1015
Product name: 3,4,4'-Trichlorocarbanilide
Purity: >98.0%(HPLC)(N)
Packaging: 500g
Price: $317
Updated: 2024/03/01

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Triclocarban Chemical Properties,Usage,Production

Chemical Properties

white crystals or powder

Originator

Cutisan,Innothera,France,1960

Uses

Labelled Triclocarban

Uses

Used as bacteriostat and antiseptic in soaps and other cleansing compositions. Antiseptic, disinfectant.

Definition

ChEBI: A member of the class of ureas that is urea substituted by a 4-chlorophenyl and a 3,4-dichlorophenyl group at positions 1 and 3 respectively.

Manufacturing Process

To a suitable reaction vessel equipped with a thermometer, agitator and reflux condenser and containing 8.1 parts by weight (substantially 0.05 mol) of 3,4-dichloroaniline in approximately 57 parts by weight of diethyl ether is added dropwise a solution of 7.7 parts by weight (substantially 0.05 mol) of 4- chlorophenyl isocyanate in approximately 15 parts by weight of diethyl ether at such a rate so as to maintain gentle reflux. Upon completion of the isocyanate addition the reaction mass is agitated for about one hour. The mass is filtered and the residue washed with diethyl ether. The dried product is a white fluffy solid which on recrystallization from ethanol gives fine white plates of 4,3',4'-trichlorocarbanilide, melting point 255.2°C to 256.0°C (88.0% yield)

Therapeutic Function

Disinfectant

General Description

Fine white plates or white powder.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

A halogenated amide. Organic amides/imides react with azo and diazo compounds to generate toxic gases. Flammable gases are formed by the reaction of organic amides/imides with strong reducing agents. Amides are very weak bases (weaker than water). Imides are less basic yet and in fact react with strong bases to form salts. That is, they can react as acids. Mixing amides with dehydrating agents such as P2O5 or SOCl2 generates the corresponding nitrile. The combustion of these compounds generates mixed oxides of nitrogen (NOx).

Fire Hazard

The flash point of Triclocarban has not been determined. Triclocarban is, however, probably combustible.

Flammability and Explosibility

Non flammable

Biochem/physiol Actions

3,4,4′-Trichlorocarbanilide interferes with mammalian reproduction and can cause methemoglobinemia in humans.

Safety Profile

Moderately toxic byintraperitoneal route. When heated to decomposition itemits very toxic fumes of Clí and NOx.

Triclocarban Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from Triclocarban manufacturers

HebeiShuoshengImportandExportco.,Ltd

Product: Triclosan 101-20-2
Price: US $6.00/kg
Min. Order: 1kg
Purity: 99%
Supply Ability: 2000KG/Month
Release date: 2024-08-07

Hebei Zhuanglai Chemical Trading Co.,Ltd

Product: Triclocarban TCC 101-20-2
Price: US $85.00-35.00/kg
Min. Order: 1kg
Purity: 99%
Supply Ability: 20ton
Release date: 2024-05-24

Hebei Longbang Technology Co., Ltd

Product: Triclocarban 101-20-2
Price: US $6.00/kg
Min. Order: 1kg
Purity: More than 99%
Supply Ability: 2000KG/Month
Release date: 2024-05-08

101-20-2, TriclocarbanRelated Search:

Triclosan Trichloroethylene Trichlorosilane UREA-13C Trichloroisocyanuric acid Sucralose Trichloroacetic acid CERIUM(III) CHLORIDE NEODYMIUM CHLORIDE Phosphorus oxychloride Trichloroacetonitrile Aluminum chloride Trichloroacetyl chloride Chlorobutanol VANADIUM(V) TRICHLORIDE OXIDE 4-Chlorophenylurea Chloroform UREA HYDROCHLORIDE

TCC

solubacter

Procutene

N-(3,4-DICHLOROPHENYL)-N'-(4-CHLOROPHENYL)UREA

N-(4-CHLOROPHENYL)-N-(3,4-DICHLOROPHENYL)-UREA

TRICHLOROCARBANILIDE

TRICLOCARBAN

Carbanilide, 3,4,4'-trichloro-

CP 78416

ENT 26925

ent26925

n-(4-chlorophenyl)-n’-(3,4-dichlorophenyl)-ure

3,4,4’-trichloro-carbanilid

Triclo Carban/TriChloro Cabanilide

genoface

cusiter

CUTISAN

1-(4-CHLOROPHENYL)-3-(3,4-DICHLOROPHENYL)UREA

1-(3',4'-Dichlorophenyl)-3-(4'-chlorophenyl)urea

Nipaguard DME

Nipaguard TCC

Nobacter

NSC-72005

tcc(soapbacteriostat)

Trilocarban

Urea, N-(4-chlorophenyl)-N'-(3,4-dichlorophenyl)-

3,4,4'-Trichlorodiphenylurea Triclocarban

Triclocarban-d4

TCC)3,4,4'-Trichloroc

3, 4, 4' -trichlorocarbanilide, Trichlorocarbanilide, N-(4-chlorophenyl)-N'-(3,4-dichlorophenyl) urea

Three chlorinebreakouts

Triclocarban 0

3,4,4 TRICHLOROCARBANILIDE

3,4,4'-TRICHLOROCARBANILIDE

3,4,4'-TRICHLORODIPHENYLUREA

Tricloarban

Trichlorocarbon

Triclocarban(Tcc)98%

Kangjiexin(Tcc)TriclocarbanC13H9Cl3N2O3,4,4'-Trichlorocarbanilide

Trichlorocarbon(Tcc)

Triclocarban(Trichlorocarbanilide)

SuperiorTccC13H9Cl3N2OTriclocarban3,4,4'-Trichlorocarbanilide

Kangjiexin (Tcc) Triclocarban 3,4,4'—Trichlorocarbanilide

Triclocarban (Tcc) 98%

3,4,4'—Trichlorocarbanilide (Triclocarban)

3,4,4''TRICHLOROCARBANILIDE/KANGJIEXIN(TCC)

TRICHLOCARBAN

3,4,4''.-TRICLOCARBAN( TRICHLOROCARBANILIDE ) 98+%

TRICLOCARBAN (3,4,4''-TRICHLOROCARBANILIDE)

TRICLOSCARBAN

TRICLOCARBAN (3, 4, 4''-TRICHLOROCARBANILIDE, TCC)

1-(4-Chlorophenyl)-3-(3,4-dichlorophenyl)urea, TCC, Triclocarban

3,4,4′-Trichlorocarbanilide,1-(4-Chlorophenyl)-3-(3,4-dichlorophenyl)urea, TCC, Triclocarban

Trichloro-diphenyl urea are

3,4,4'richlorocarbanilide(Triclocarban)

4′-Trichlorocarbanilide

Chemical class card

Triclocarban Solution in Methanol, 100μg/mL