MedKoo Cat#: 161239 | Name: 2,2′-Dipyrromethane
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

2,2′-Dipyrromethane is a porphyrin building block, used in synthesizing porphyrins and related biochemicals.

Chemical Structure

2,2′-Dipyrromethane
2,2′-Dipyrromethane
CAS#21211-65-4

Theoretical Analysis

MedKoo Cat#: 161239

Name: 2,2′-Dipyrromethane

CAS#: 21211-65-4

Chemical Formula: C9H10N2

Exact Mass: 146.0844

Molecular Weight: 146.19

Elemental Analysis: C, 73.94; H, 6.89; N, 19.16

Price and Availability

Size Price Availability Quantity
1g USD 485.00 2 Weeks
5g USD 885.00 2 Weeks
10g USD 1,335.00 2 Weeks
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Related CAS #
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Synonym
2,2′-Dipyrromethane; 2, 2′-Dipyrromethane; di(1H-pyrrol-2-yl)methane;
IUPAC/Chemical Name
di(1H-pyrrol-2-yl)methane
InChi Key
PBTPREHATAFBEN-UHFFFAOYSA-N
InChi Code
InChI=1S/C9H10N2/c1-3-8(10-5-1)7-9-4-2-6-11-9/h1-6,10-11H,7H2
SMILES Code
C1(CC2=CC=CN2)=CC=CN1
Appearance
To be determined
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 -4 C for short term (days to weeks) or -20 C for long term(months to years).
Solubility
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 146.19 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1.) Banfi, et al. Comparison between 5,10,15,20-Tetraaryl- and 5,15-Diarylporphyrins as Photosensitizers:  Synthesis, Photodynamic Activity, and Quantitative Structure−Activity Relationship Modeling. J. Med. Chem. 2006, 49, 11, 3293–3304. https://doi.org/10.1021/jm050997m 2.) Goncalves, et al. Synthesis and G-quadruplex binding studies of new 4-N-methylpyridinium porphyrins. Org. Biomol. Chem., 2006,4, 3337-3342. https://doi.org/10.1039/B608494J