1219799-29-7
1219799-29-7
Chemical Structure
Triclocarban-d4
Synonym(s): 3,4,4′-Trichlorocarbanilide-d4
- CAS No.: 1219799-29-7
- Formula:C13H5D4Cl3N2O
- Molecular Weight:319.61
IUPAC Name: 1-(4-chlorophenyl-2,3,5,6-d4)-3-(3,4-dichlorophenyl)urea
InChIKey: ICUTUKXCWQYESQ-RHQRLBAQSA-N
SMILES: ClC(C([2H])=C1[2H])=C([2H])C([2H])=C1NC(NC2=CC(Cl)=C(C=C2)Cl)=O
Biological Activity: Triclocarban-d4 is the deuterium labeled Triclocarban. Triclocarban (3,4,4′-Trichlorocarbanilide), a broad spectrum antibacterial compound, is widely used in a broad range of applications such as the production of soaps, skin creams, toothpastes and deodorants. Triclocarban is a potential endocrine-disrupting chemical with the capacity to modulate androgen and estrogen activities as well as other hormone-mediated biological processes[1][2][3].
| Cat. No. | Nom du produit | Pureté | Description | Pricing | |||||||||||||||||||
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Triclocarban-d4 | 98.09% | Triclocarban-d4 is the deuterium labeled Triclocarban. Triclocarban (3,4,4′-Trichlorocarbanilide), a broad spectrum antibacterial compound, is widely used in a broad range of applications such as the production of soaps, skin creams, toothpastes and deodorants. Triclocarban is a potential endocrine-disrupting chemical with the capacity to modulate androgen and estrogen activities as well as other hormone-mediated biological processes. | ||||||||||||||||||||
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Triclocarban (Standard) | 99.15% | Triclocarban (Standard) (3,4,4′-Trichlorocarbanilide (Standard)) is the analytical standard of Triclocarban (HY-B1805). This product is intended for research and analytical applications. Triclocarban, a broad spectrum antibacterial compound, is widely used in a broad range of applications such as the production of soaps, skin creams, toothpastes and deodorants. Triclocarban is a potential endocrine-disrupting chemical with the capacity to modulate androgen and estrogen activities as well as other hormone-mediated biological processes. | ||||||||||||||||||||
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Triclocarban-13C6 | Triclocarban-13C6 is the 13C labeled isotope of Triclocarban (HY-B1805). Triclocarban (3,4,4′-Trichlorocarbanilide), a broad spectrum antibacterial compound, is widely used in a broad range of applications such as the production of soaps, skin creams, toothpastes and deodorants. Triclocarban is a potential endocrine-disrupting chemical with the capacity to modulate androgen and estrogen activities as well as other hormone-mediated biological processes. | |||||||||||||||||||||
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Triclocarban-13C13 | Triclocarban-13C13 (3,4,4'-Trichlorocarbanilide-13C13) is 13C labeled Triclocarban. Triclocarban (3,4,4′-Trichlorocarbanilide), a broad spectrum antibacterial compound, is widely used in a broad range of applications such as the production of soaps, skin creams, toothpastes and deodorants. Triclocarban is a potential endocrine-disrupting chemical with the capacity to modulate androgen and estrogen activities as well as other hormone-mediated biological processes. | |||||||||||||||||||||
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Triclocarban | 98.93% | Triclocarban (3,4,4′-Trichlorocarbanilide), a broad spectrum antibacterial compound, is widely used in a broad range of applications such as the production of soaps, skin creams, toothpastes and deodorants. Triclocarban is a potential endocrine-disrupting chemical with the capacity to modulate androgen and estrogen activities as well as other hormone-mediated biological processes. | ||||||||||||||||||||
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References
- [1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. [Content Brief]
- [2]. Kanbara Y, et al. Nanomolar concentration of triclocarban increases the vulnerability of rat thymocytes to oxidative stress. J Toxicol Sci. 2013 Feb;38(1):49-55. [Content Brief]
- [3]. Huang H, et al. The in vitro estrogenic activities of triclosan and triclocarban. J Appl Toxicol. 2014 Sep;34(9):1060-7. [Content Brief]
