3,4,4'-trichlorocarbanilide (CAS 101-20-2) — formula C13H9Cl3N2O, molecular weight 315.6; category organic chemicals.
| CAS Number | 101-20-2 |
|---|---|
| Molecular Formula | C13H9Cl3N2O |
| Molecular Weight | 315.6 |
| Melting Point | 482 to 493 °F (NTP, 1992) |
| Boiling Point | 250 °C at 97.8 kPa (733 mm Hg) |
| LogP | log Kow = 4.342 at 25 °C, pH 8.1 |
| Applications | Uses: Used as an antiseptic in cleaning products, [Merck Index] Used for skin and mucous membrane disinfection, [Reference #1], Using Disinfectants or Biocides [Category: Clean], For 3, 4, 4'-trichlorocarbanilide (USEPA, OPP Pesticide Code: 027901) there are 0 labels match., SRP: Not registered for current use in the U.S., but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Bacteriostat and antiseptic in soaps and other cleansing compositions., Bacteriostat in ... plastics., Triclocarban is an anti-microbial active ingredient used globally in a wide range of personal cleansing products that include deodorant soaps, detergents, cleansing lotions, and wipes. In North America, triclocarban is used exclusively as an antimicrobial and preservative in bar and liquid soaps and body washes., Deodorant soaps contain an active ingredient such as 3, 4'-trichlorocarbanilide (trichlocarban) to inhibit the growth of skin bacteria responsible for the formation of odor-causing substances from perspiration, Use Classification: Cosmetics -> Preservative, Household Products: Information on 23 consumer products that contain Triclocarban in the following categories is provided:, • Personal Care, Methods of Manufacturing: There are two commercial routes used for the production of triclocarban: 4-chlorophenyl isocyanate is reacted with 3, 4-dichloroaniline to give triclocarban, or 3, 4-dichlorophenyl isocyanate is reacted with 4-chloroaniline to give triclocarban., Preparation from 3, 4-dichloroaniline and 4-chlorophenyl isocyanate ... Beaver, Stoffel, United States of America patent 2818390 (1957 to Monsanto), United Kingdom patent 769273 (1957)., U.S. Production: (1977) PROBABLY GREATER THAN 2.27X10+6 GRAMS, (1979) PROBABLY GREATER THAN 2.27X10+6 GRAMS, 3, 4'-Trichlorocarbanilide is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and, or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B, 51FR21438)., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#5004], For more U.S. Production (Complete) data for Triclocarban (6 total), please visit the HSDB record page., U.S. Imports: (1977) No Data, (1979) No Data, U.S. Exports: (1977) No Data, General Manufacturing Information: Urea, N-(4-chlorophenyl)-N'-(3, 4-dichlorophenyl)-: ACTIVE, TCC is primarily effective against gram-positive bacteria. |
| Category | Organic Chemicals |
Documented applications: Uses: Used as an antiseptic in cleaning products, [Merck Index] Used for skin and mucous membrane disinfection, [Reference #1], Using Disinfectants or Biocides [Category: Clean], For 3, 4, 4'-trichlorocarbanilide (USEPA, OPP Pesticide Code: 027901) there are 0 labels match., SRP: Not registered for current use in the U.S., but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Bacteriostat and antiseptic in soaps and other cleansing compositions., Bacteriostat in ... plastics., Triclocarban is an anti-microbial active ingredient used globally in a wide range of personal cleansing products that include deodorant soaps, detergents, cleansing lotions, and wipes. In North America, triclocarban is used exclusively as an antimicrobial and preservative in bar and liquid soaps and body washes., Deodorant soaps contain an active ingredient such as 3, 4'-trichlorocarbanilide (trichlocarban) to inhibit the growth of skin bacteria responsible for the formation of odor-causing substances from perspiration, Use Classification: Cosmetics -> Preservative, Household Products: Information on 23 consumer products that contain Triclocarban in the following categories is provided:, • Personal Care, Methods of Manufacturing: There are two commercial routes used for the production of triclocarban: 4-chlorophenyl isocyanate is reacted with 3, 4-dichloroaniline to give triclocarban, or 3, 4-dichlorophenyl isocyanate is reacted with 4-chloroaniline to give triclocarban., Preparation from 3, 4-dichloroaniline and 4-chlorophenyl isocyanate ... Beaver, Stoffel, United States of America patent 2818390 (1957 to Monsanto), United Kingdom patent 769273 (1957)., U.S. Production: (1977) PROBABLY GREATER THAN 2.27X10+6 GRAMS, (1979) PROBABLY GREATER THAN 2.27X10+6 GRAMS, 3, 4'-Trichlorocarbanilide is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and, or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B, 51FR21438)., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#5004], For more U.S. Production (Complete) data for Triclocarban (6 total), please visit the HSDB record page., U.S. Imports: (1977) No Data, (1979) No Data, U.S. Exports: (1977) No Data, General Manufacturing Information: Urea, N-(4-chlorophenyl)-N'-(3, 4-dichlorophenyl)-: ACTIVE, TCC is primarily effective against gram-positive bacteria..
3,4,4'-trichlorocarbanilide is a carbon-based organic compound with CAS registry number 101-20-2 and molecular formula C13H9Cl3N2O (molecular weight 315.6), belonging to the organic chemicals segment of chemical raw materials.
CAS number: 101-20-2
Its molecular formula C13H9Cl3N2O comprises 13 C, 9 H, 3 Cl, 2 N, 1 O atoms.
Also known as: 3,4,4'-trichlorocarbanilide · Triclocarban · TCC
Category: organic chemicals
The CAS registry number of 3,4,4'-trichlorocarbanilide is 101-20-2.
Molecular formula C13H9Cl3N2O, molecular weight 315.6.
It is also registered under: 3,4,4'-trichlorocarbanilide, Triclocarban, TCC.
Recorded applications: Uses: Used as an antiseptic in cleaning products, [Merck Index] Used for skin and mucous membrane disinfection, [Reference #1], Using Disinfectants or Biocides [Category: Clean], For 3, 4, 4'-trichlorocarbanilide (USEPA, OPP Pesticide Code: 027901) there are 0 labels match., SRP: Not registered for current use in the U.S., but approved pesticide uses may change periodically and so federal, state and local authorities must be consulted for currently approved uses., Bacteriostat and antiseptic in soaps and other cleansing compositions., Bacteriostat in ... plastics., Triclocarban is an anti-microbial active ingredient used globally in a wide range of personal cleansing products that include deodorant soaps, detergents, cleansing lotions, and wipes. In North America, triclocarban is used exclusively as an antimicrobial and preservative in bar and liquid soaps and body washes., Deodorant soaps contain an active ingredient such as 3, 4'-trichlorocarbanilide (trichlocarban) to inhibit the growth of skin bacteria responsible for the formation of odor-causing substances from perspiration, Use Classification: Cosmetics -> Preservative, Household Products: Information on 23 consumer products that contain Triclocarban in the following categories is provided:, • Personal Care, Methods of Manufacturing: There are two commercial routes used for the production of triclocarban: 4-chlorophenyl isocyanate is reacted with 3, 4-dichloroaniline to give triclocarban, or 3, 4-dichlorophenyl isocyanate is reacted with 4-chloroaniline to give triclocarban., Preparation from 3, 4-dichloroaniline and 4-chlorophenyl isocyanate ... Beaver, Stoffel, United States of America patent 2818390 (1957 to Monsanto), United Kingdom patent 769273 (1957)., U.S. Production: (1977) PROBABLY GREATER THAN 2.27X10+6 GRAMS, (1979) PROBABLY GREATER THAN 2.27X10+6 GRAMS, 3, 4'-Trichlorocarbanilide is listed as a High Production Volume (HPV) chemical (65FR81686). Chemicals listed as HPV were produced in or imported into the U.S. in >1 million pounds in 1990 and, or 1994. The HPV list is based on the 1990 Inventory Update Rule. (IUR) (40 CFR part 710 subpart B, 51FR21438)., Production volumes for non-confidential chemicals reported under the Inventory Update Rule. [Table#5004], For more U.S. Production (Complete) data for Triclocarban (6 total), please visit the HSDB record page., U.S. Imports: (1977) No Data, (1979) No Data, U.S. Exports: (1977) No Data, General Manufacturing Information: Urea, N-(4-chlorophenyl)-N'-(3, 4-dichlorophenyl)-: ACTIVE, TCC is primarily effective against gram-positive bacteria..
Category: Organic Chemicals.
Independent reference data for 3,4,4'-trichlorocarbanilide (CAS 101-20-2), compiled from public chemistry databases.
| CAS Registry Number | 101-20-2 |
|---|---|
| PubChem CID | 7547 |
| Molecular formula | C13H9Cl3N2O |
| IUPAC name | 1-(4-chlorophenyl)-3-(3,4-dichlorophenyl)urea |
| UNII (FDA) | BGG1Y1ED0Y |
| Molecular Weight | 315.6 |
|---|---|
| XLogP3 | 5.3 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 2 |
| Exact Mass | 313.978046 |
| Monoisotopic Mass | 313.978046 |
| Topological Polar Surface Area | 41.1 |
| Heavy Atom Count | 19 |
| Boiling Point | 250 °C at 97.8 kPa (733 mm Hg) |
|---|---|
| Melting Point | 482 to 493 °F (NTP, 1992) |
| Melting Point | 491.2- 493 |
| Melting Point | 254.4 °C |
| Melting Point | MP: 255.2-256 °C |
| Solubility | In water, 0.11 mg/L at 20 °C |
| Solubility | In methanol, 1.6 g/L at 35 °C |
| Density | 0.336 g/cu cm at 20 °C |
| LogP | log Kow = 4.342 at 25 °C, pH 8.1 |
| Dissociation Constants | pKa = 12.7 |
Triclocarban; 101-20-2; 1-(4-Chlorophenyl)-3-(3,4-dichlorophenyl)urea; 3,4,4'-TRICHLOROCARBANILIDE; Cutisan; Procutene; Solubacter; Cusiter; Genoface; Trilocarban; Urea, N-(4-chlorophenyl)-N'-(3,4-dichlorophenyl)-; 3,4,4'-Trichlorodiphenylurea; Trichlocarban; Triclocarbanum; N-(4-Chlorophenyl)-N'-(3,4-dichlorophenyl)urea; NSC-72005
| Regulatory & Food Contact | CIR / INCI: Preservative |
|---|
| Reported hazard statements | H400 (96.8%), H410 (100%) |
|---|
H400 (96.8%): Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard]
H410 (100%): Very toxic to aquatic life with long lasting effects [Warning Hazardous to the aquatic environment, long-term hazard]
3,4,4'-trichlorocarbanilide · CAS 101-20-2 · C13H9Cl3N2O. UNII BGG1Y1ED0Y. Boiling Point: 250 °C at 97.8 kPa (733 mm Hg); Melting Point: 482 to 493 °F (NTP, 1992); Melting Point: 491.2- 493.
Source: PubChem / Wikidata; the batch COA governs where values differ.
Supplier: Jinan Shenghe Chemical Co., Ltd.