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C8895

Clofazimine

≥98% (TLC), powder, antimycobacterial rimonphenazine

Synonym(s):

N,5-Bis(4-chlorophenyl)-3,5-dihydro-3-(isopropylimino)phenazin-2-amine

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About This Item

Empirical Formula (Hill Notation):
C27H22Cl2N4
CAS Number:
Molecular Weight:
473.40
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
EC Number:
217-980-2
MDL number:
Form:
powder
Quality level:
Pricing and availability is not currently available.
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Product Name

Clofazimine,

form

powder

Quality Level

antibiotic activity spectrum

mycobacteria

mode of action

protein synthesis | interferes

originator

Novartis

SMILES string

CC(C)\N=C1/C=C2N(c3ccc(Cl)cc3)c4ccccc4N=C2C=C1Nc5ccc(Cl)cc5

InChI

1S/C27H22Cl2N4/c1-17(2)30-24-16-27-25(15-23(24)31-20-11-7-18(28)8-12-20)32-22-5-3-4-6-26(22)33(27)21-13-9-19(29)10-14-21/h3-17,31H,1-2H3/b30-24+

InChI key

WDQPAMHFFCXSNU-BGABXYSRSA-N

General description

Clofazimine is a riminophenazine, which is used as an antileprosy drug. It is used to treat multidrug-resistant tuberculosis. Clofazimine prevents neutrophil motility and lymphocyte transformation. It has anti-inflammatory effect, which is used to treat discoid lupus erythematosus. Clofazimine has immunosuppressive property.

Application

Clofazimine has been used:
  • for antimicrobial preparation
  • to study its accumulation on macrophages to form crystal-like drug inclusions (CLDIs)
  • to model drug-induced hepatic granulomatous inflammation
  • to study the in vivo cargo storage capacity of macrophages

Features and Benefits

This compound was developed by Novartis. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Preparation Note

This product is stored at room temperature.

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This Item
Y00003131138904BP663
form

powder

form

-

form

-

form

solid

Quality Level

200

Quality Level

-

Quality Level

-

Quality Level

-

originator

Novartis

originator

-

originator

-

originator

-

antibiotic activity spectrum

mycobacteria

antibiotic activity spectrum

-

antibiotic activity spectrum

-

antibiotic activity spectrum

-

mode of action

protein synthesis | interferes

mode of action

-

mode of action

-

mode of action

-


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Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves



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A far-red fluorescent probe for flow cytometry and image-based functional studies of xenobiotic sequestering macrophages
Keswani RK, et al.
Cytometry. Part A : the Journal of the International Society For Analytical Cytology, 87(9), 855-867 (2015)
In vitro approaches for generation of Mycobacterium tuberculosis mutants resistant to bedaquiline, clofazimine or linezolid and identification of associated genetic variants
Ismail N, et al.
Journal of Microbiological Methods, 153(8), 1-9 (2018)
An Expandable Mechanopharmaceutical Device (1): Measuring the Cargo Capacity of Macrophages in a Living Organism
Rzeczycki P, et al.
Pharmaceutical Research, 36(1), 12-12 (2019)



Global Trade Item Number

SKUGTIN
C8895-1G04061833522981
C8895-5G04061833522998

Questions

1–2 of 2 Questions  
  1. What is the recommended solvent that is compatible for in vitro culture of mammalian cells?

    1 answer
    1. The solubility of this product has been tested in chloroform at a concentration of 50 mg/mL. For cell culture application, it can be dissolved in fresh, anhydrous DMSO at 5 mg/mL (10.56 mM), but the final concentration of DMSO in cell culture should not exceed more than 0.1%. Most cells can tolerate up to 0.1% DMSO; however, the response may vary depending on the specific type of cell or cell line. Therefore, it is advisable to conduct preliminary testing to determine the optimal concentration for your particular application.

      Helpful?

  2. At what temperature should this be stored? I so not see a specified temperature on label or SDS so I would assume room temperature but other manufacturers of this product claim -20C

    1 answer
    1. This product is stored at room temperature.

      Helpful?

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