accessibility menu, dialog, popup

UserName
Viewing profile as user:

Organoheterocyclic compounds

Organic compounds that consist of ring structures, or cyclic compounds that have atoms of at least two different elements as members of its ring(s).
Pyridines and derivatives (12)
Heteroaromatic compounds (1)

Filtered Search Results

Products from some of our suppliers do not display in filtered search results. Please clear all filters to see these products.

Narrow Results

Selected Filters

Clear all

Keyword Search

iridium

Narrow Results

Narrow Results

No results found within this category. Try removing some selected filters and try again.

category

brands

  • (5)
  • (4)
  • (1)
  • (3)

special interests

  • (3)

Molecular Weight (g/mol)

  • (1)
  • (1)
  • (1)

Percent Purity

  • (1)
  • (1)
  • (1)

Physical Form

  • (3)

Quantity

  • (1)
  • (2)
1 – 13 of 13 results
1

Tris(2-phenylpyridinato)iridium(III) (purified by sublimation) 95.0+%, TCI America™
SDP

CAS: 94928-86-6 Molecular Formula: C33H24IrN3 Molecular Weight (g/mol): 654.793 MDL Number: MFCD04039766 InChI Key: NSABRUJKERBGOU-UHFFFAOYSA-N Synonym: Ir(ppy)3 PubChem CID: 59117881 IUPAC Name: iridium(3+);2-phenylpyridine SMILES: C1=CC=C([C-]=C1)C2=CC=CC=N2.C1=CC=C([C-]=C1)C2=CC=CC=N2.C1=CC=C([C-]=C1)C2=CC=CC=N2.[Ir+3]

PubChem CID 59117881
CAS 94928-86-6
Molecular Weight (g/mol) 654.793
MDL Number MFCD04039766
SMILES C1=CC=C([C-]=C1)C2=CC=CC=N2.C1=CC=C([C-]=C1)C2=CC=CC=N2.C1=CC=C([C-]=C1)C2=CC=CC=N2.[Ir+3]
Synonym Ir(ppy)3
IUPAC Name iridium(3+);2-phenylpyridine
InChI Key NSABRUJKERBGOU-UHFFFAOYSA-N
Molecular Formula C33H24IrN3
2

Tris[1-phenylisoquinoline-C2,N]iridium(III) (purified by sublimation) 99.0+%, TCI America™
SDP

CAS: 435293-93-9 Molecular Formula: C45H30IrN3 Molecular Weight (g/mol): 804.973 MDL Number: MFCD09842770 InChI Key: NDBCGHNTWCYIIU-UHFFFAOYSA-N Synonym: Ir(piq)3 PubChem CID: 53384374 IUPAC Name: iridium(3+);1-phenylisoquinoline SMILES: C1=CC=C([C-]=C1)C2=NC=CC3=CC=CC=C32.C1=CC=C([C-]=C1)C2=NC=CC3=CC=CC=C32.C1=CC=C([C-]=C1)C2=NC=CC3=CC=CC=C32.[Ir+3]

PubChem CID 53384374
CAS 435293-93-9
Molecular Weight (g/mol) 804.973
MDL Number MFCD09842770
SMILES C1=CC=C([C-]=C1)C2=NC=CC3=CC=CC=C32.C1=CC=C([C-]=C1)C2=NC=CC3=CC=CC=C32.C1=CC=C([C-]=C1)C2=NC=CC3=CC=CC=C32.[Ir+3]
Synonym Ir(piq)3
IUPAC Name iridium(3+);1-phenylisoquinoline
InChI Key NDBCGHNTWCYIIU-UHFFFAOYSA-N
Molecular Formula C45H30IrN3
3

(4,4'-Di-tert-butyl-2,2'-bipyridine)bis[(2-pyridinyl)phenyl]iridium(III) Hexafluorophosphate 85.0+%, TCI America™
SDP

CAS: 676525-77-2 Molecular Formula: C40H40F6IrN4P Molecular Weight (g/mol): 913.969 InChI Key: VCIVELSSYHAWGC-UHFFFAOYSA-N PubChem CID: 44239994 IUPAC Name: 4-tert-butyl-2-(4-tert-butylpyridin-2-yl)pyridine;iridium(3+);2-phenylpyridine;hexafluorophosphate SMILES: CC(C)(C)C1=CC(=NC=C1)C2=NC=CC(=C2)C(C)(C)C.C1=CC=C([C-]=C1)C2=CC=CC=N2.C1=CC=C([C-]=C1)C2=CC=CC=N2.F[P-](F)(F)(F)(F)F.[Ir+3]

PubChem CID 44239994
CAS 676525-77-2
Molecular Weight (g/mol) 913.969
SMILES CC(C)(C)C1=CC(=NC=C1)C2=NC=CC(=C2)C(C)(C)C.C1=CC=C([C-]=C1)C2=CC=CC=N2.C1=CC=C([C-]=C1)C2=CC=CC=N2.F[P-](F)(F)(F)(F)F.[Ir+3]
IUPAC Name 4-tert-butyl-2-(4-tert-butylpyridin-2-yl)pyridine;iridium(3+);2-phenylpyridine;hexafluorophosphate
InChI Key VCIVELSSYHAWGC-UHFFFAOYSA-N
Molecular Formula C40H40F6IrN4P
4

Ambeed Iridium 1 4 4 bis 1 1dimet

Iridium(1+), [4,4'-bis(1,1-dimethylethyl)-2,2'-bipyridine-κN1,κN1']bis[3-fluoro-5-(trifluoromethyl)-2-[5-(trifluoromethyl)-2-pyridinyl-κN]phenyl-κC]-, (OC-6-33)-, hexafluorophosphate(1-) (1:1), 2222402-20-0, 98%

ENCOMPASS_PREFERRED
5

Ambeed Iridium 1 4 4 bis 1 1dimet

Iridium(1+), [4,4'-bis(1,1-dimethylethyl)-2,2'-bipyridine-κN1,κN1']bis[3-fluoro-5-(trifluoromethyl)-2-[5-(trifluoromethyl)-2-pyridinyl-κN]phenyl-κC]-, (OC-6-33)-, hexafluorophosphate(1-) (1:1), 2222402-20-0, 98%

ENCOMPASS_PREFERRED
6

Ambeed Iridium 1 4 4 bis 1 1dimet

Iridium(1+), [4,4'-bis(1,1-dimethylethyl)-2,2'-bipyridine-κN1,κN1']bis[3-fluoro-5-(trifluoromethyl)-2-[5-(trifluoromethyl)-2-pyridinyl-κN]phenyl-κC]-, (OC-6-33)-, hexafluorophosphate(1-) (1:1), 2222402-20-0, 98%

ENCOMPASS_PREFERRED
7

Ambeed Iridium 1 4 4 bis 1 1dimet

Iridium(1+), [4,4'-bis(1,1-dimethylethyl)-2,2'-bipyridine-κN1,κN1']bis[3-fluoro-5-(trifluoromethyl)-2-[5-(trifluoromethyl)-2-pyridinyl-κN]phenyl-κC]-, (OC-6-33)-, hexafluorophosphate(1-) (1:1), 2222402-20-0, 98%

ENCOMPASS_PREFERRED
8

Ambeed Iridium 1 4 4 bis 1 1dimet

Iridium(1+), [4,4'-bis(1,1-dimethylethyl)-2,2'-bipyridine-κN1,κN1']bis[3-fluoro-5-(trifluoromethyl)-2-[5-(trifluoromethyl)-2-pyridinyl-κN]phenyl-κC]-, (OC-6-33)-, hexafluorophosphate(1-) (1:1), 2222402-20-0, 98%

ENCOMPASS_PREFERRED
9

Medchemexpress LLC Pentamethylcyclopentadienyl iridium(III) chloride dimer | 12354-84-6 | MFCD00075435 | 98.0% | 796.70 | C20H30Cl4Ir2 | 50 MG

[Ir(Cp-)Cl2]2 is an organometallic iridium(III) chloride dimer used as a precursor to catalysts for asymmetric transfer hydrogenation of ketones and in the synthesis of amines. It is supplied as an orange to reddish-brown solid for research use and requires light protection and inert storage.

  • Used as a precursor for asymmetric transfer hydrogenation catalysts.
  • Applicable in greener amine synthesis reactions.
  • Orange to reddish-brown solid, suitable for small-scale research.
  • Store at 4°C, protect from light, and keep under nitrogen for stability.
  • For research use only; not intended for human or patient use.

ENCOMPASS_PREFERRED
10

Medchemexpress LLC Dichloro(pentamethylcyclopentadienyl)iridium(III) dimer | 12354-84-6 | MFCD00075435 | ≥99.0% | 796.70 g·mol⁻¹ | C20H30Cl4Ir2 | 100 MG

[Ir(Cp-)Cl2]2 (dichloro(pentamethylcyclopentadienyl)iridium(III) dimer) is an organometallic iridium complex supplied for research use. It serves as a precursor to catalysts for asymmetric transfer hydrogenation of ketones and is employed in catalytic amine synthesis. The compound is a solid, typically orange to reddish brown, with formula C20H30Cl4Ir2 and an approximate molecular weight of 796.70 g·mol⁻¹.

  • High purity ≥99.0% suitable for research and synthetic applications.
  • Precursor for asymmetric transfer hydrogenation catalysts.
  • Useful catalyst for greener amine synthesis and related transformations.
  • Orange to reddish brown solid offering easy handling and storage.
  • Chemical identity confirmed by CAS number and molecular formula for traceability.

ENCOMPASS_PREFERRED
11

Strem, An Ascensus Company CAS 405235-55-4. 500mg. ((4S5S)-(-)-O-[1-Benzyl-1-(5-methyl-2-phenyl-45-dihydrooxazol-4-yl)-2-phenylethyl]-diphenylphosphinite)(15-COD)iridium(I) tetrakis(35-bis(trifluoromethyl)phenylborate min. 97% (SS)-[COD]Ir[Ph2PThrePHOX]. MFCD06658140

CAS 405235-55-4. 500mg. ((4S5S)-(-)-O-[1-Benzyl-1-(5-methyl-2-phenyl-45-dihydrooxazol-4-yl)-2-phenylethyl]-diphenylphosphinite)(15-COD)iridium(I) tetrakis(35-bis(trifluoromethyl)phenylborate min. 97% (SS)-[COD]Ir[Ph2PThrePHOX]. MFCD06658140. Molecular Weight 1719.25. Molecular Formula Ir(C8H12)(C37H34NO2P)B[C6H3(CF3)2]4ae. Color/form orange pwdr. Strem 77-5020. http//www.strem.com/catalog/v/77-5020/

ENCOMPASS
12

Medchemexpress LLC NecroIr2 | 99.0% | 926.44 | C46H30ClIrN6O2- | 10 MG

NecroIr2 is an iridium(III) complex necroptosis inducer active in cisplatin-resistant lung cancer (A549R) cells. It selectively accumulates in mitochondria, triggers oxidative stress and loss of mitochondrial membrane potential, activates RIPK3 and MLKL, and modulates CDK4 expression. Intended for laboratory research use.

  • Iridium(III) complex with mitochondrial accumulation.
  • Induces necroptosis in cisplatin-resistant lung cancer cells.
  • Activates RIPK3 and MLKL signaling pathways.
  • Causes oxidative stress and loss of mitochondrial membrane potential.
  • Supplied in multiple pack sizes and high purity for research applications.
  • Store sealed away from moisture and light; use cold storage for solutions.

ENCOMPASS_PREFERRED
13

Medchemexpress LLC NecroIr1 | 98.0% | 823.36 g/mol | C40H29ClIrN5O | 10 MG

NecroIr1 is an iridium(III) coordination complex used as a research reagent to induce necroptosis in cisplatin-resistant lung cancer cells (A549R). It preferentially accumulates in mitochondria, promotes reactive oxygen species (ROS) generation and loss of mitochondrial membrane potential, activates necroptosis-associated kinases, and induces G0/G1 cell-cycle arrest that inhibits cell proliferation in vitro.

  • High purity (98.02%) suitable for cellular assays.
  • Preferential mitochondrial accumulation enabling targeted ROS generation.
  • Activates necroptosis signaling through RIPK1, RIPK3, and MLKL.
  • Induces G0/G1 cell-cycle arrest and inhibits proliferation in resistant lung cancer cells.
  • Provided as a solid 10 mg unit for laboratory studies.
  • Store sealed at 4°C; in solvent: -80°C (6 months), -20°C (1 month).

ENCOMPASS_PREFERRED