Dipyrrometheneboron difluoride

Cat. No.: HY-W442295 Purity: 95.87%: FAQs
Data Sheet SDS COA Handling Instructions

Molarity Calculator

Dipyrrometheneboron difluoride is a green-fluorescent dye used for labeling nonpolar lipids and detecting calcium.

For research use only. We do not sell to patients.

Dipyrrometheneboron difluoride Chemical Structure

CAS No. : 138026-71-8

Size	Price	Stock	Quantity
10 mg	USD 50	In-stock	Estimated Time of Arrival: December 31
25 mg	USD 101	In-stock	Estimated Time of Arrival: December 31
50 mg	USD 152	In-stock	Estimated Time of Arrival: December 31
100 mg	USD 228	In-stock	Estimated Time of Arrival: December 31
200 mg		Get quote
500 mg		Get quote

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Based on 1 publication(s) in Google Scholar

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Biological Activity
Purity & Documentation
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Description

Dipyrrometheneboron difluoride is a green-fluorescent dye used for labeling nonpolar lipids and detecting calcium.

Cellular Effect

Cell Line	Type	Value	Description	References
C2C12	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against mouse C2C12 cells after 24 hrs by WST-1 assay Cytotoxicity against mouse C2C12 cells after 24 hrs by WST-1 assay	[PMID: 25197766]
C2C12	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against mouse C2C12 cells after 48 hrs by WST-1 assay Cytotoxicity against mouse C2C12 cells after 48 hrs by WST-1 assay	[PMID: 25197766]
C2C12	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against mouse C2C12 cells after 72 hrs by WST-1 assay Cytotoxicity against mouse C2C12 cells after 72 hrs by WST-1 assay	[PMID: 25197766]
HT-29	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against human HT-29 cells after 24 hrs by WST-1 assay Cytotoxicity against human HT-29 cells after 24 hrs by WST-1 assay	[PMID: 25197766]
HT-29	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against human HT-29 cells after 48 hrs by WST-1 assay Cytotoxicity against human HT-29 cells after 48 hrs by WST-1 assay	[PMID: 25197766]
HT-29	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against human HT-29 cells after 72 hrs by WST-1 assay Cytotoxicity against human HT-29 cells after 72 hrs by WST-1 assay	[PMID: 25197766]
LNCaP	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against human LNCAP cells after 24 hrs by WST-1 assay Cytotoxicity against human LNCAP cells after 24 hrs by WST-1 assay	[PMID: 25197766]
LNCaP	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against human LNCAP cells after 48 hrs by WST-1 assay Cytotoxicity against human LNCAP cells after 48 hrs by WST-1 assay	[PMID: 25197766]
LNCaP	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against human LNCAP cells after 72 hrs by WST-1 assay Cytotoxicity against human LNCAP cells after 72 hrs by WST-1 assay	[PMID: 25197766]
MCF7	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against human MCF7 cells after 24 hrs by WST-1 assay Cytotoxicity against human MCF7 cells after 24 hrs by WST-1 assay	[PMID: 25197766]
MCF7	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against human MCF7 cells after 48 hrs by WST-1 assay Cytotoxicity against human MCF7 cells after 48 hrs by WST-1 assay	[PMID: 25197766]
MCF7	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against human MCF7 cells after 72 hrs by WST-1 assay Cytotoxicity against human MCF7 cells after 72 hrs by WST-1 assay	[PMID: 25197766]
MIA PaCa-2	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against human MIAPaCa2 cells after 24 hrs by WST-1 assay Cytotoxicity against human MIAPaCa2 cells after 24 hrs by WST-1 assay	[PMID: 25197766]
MIA PaCa-2	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against human MIAPaCa2 cells after 48 hrs by WST-1 assay Cytotoxicity against human MIAPaCa2 cells after 48 hrs by WST-1 assay	[PMID: 25197766]
MIA PaCa-2	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against human MIAPaCa2 cells after 72 hrs by WST-1 assay Cytotoxicity against human MIAPaCa2 cells after 72 hrs by WST-1 assay	[PMID: 25197766]
PC-3	IC₅₀	1.5 μM Compound: Bdp	Cytotoxicity against human PC3 cells after 24 hrs by WST-1 assay Cytotoxicity against human PC3 cells after 24 hrs by WST-1 assay	[PMID: 25197766]
PC-3	IC₅₀	3.1 μM Compound: Bdp	Cytotoxicity against human PC3 cells after 48 hrs by WST-1 assay Cytotoxicity against human PC3 cells after 48 hrs by WST-1 assay	[PMID: 25197766]
PC-3	IC₅₀	5.6 μM Compound: Bdp	Cytotoxicity against human PC3 cells after 72 hrs by WST-1 assay Cytotoxicity against human PC3 cells after 72 hrs by WST-1 assay	[PMID: 25197766]
U2OS	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against human U2OS cells after 24 hrs by WST-1 assay Cytotoxicity against human U2OS cells after 24 hrs by WST-1 assay	[PMID: 25197766]
U2OS	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against human U2OS cells after 48 hrs by WST-1 assay Cytotoxicity against human U2OS cells after 48 hrs by WST-1 assay	[PMID: 25197766]
U2OS	IC₅₀	> 50 μM Compound: Bdp	Cytotoxicity against human U2OS cells after 72 hrs by WST-1 assay Cytotoxicity against human U2OS cells after 72 hrs by WST-1 assay	[PMID: 25197766]

Molecular Weight

191.97

Formula

C₉H₇BF₂N₂

CAS No.

138026-71-8

Appearance

Solid

Color

Purple to purplish red

SMILES

[F-][B+3]1([N]2=CC=CC2=CC3=CC=C[N-]31)[F-]

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

-20°C, protect from light

*In solvent : -80°C, 6 months; -20°C, 1 month (protect from light)

Solvent & Solubility

In Vitro:

DMSO : 100 mg/mL (520.91 mM; Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Preparing
Stock Solutions

Concentration Solvent Mass	1 mg	5 mg	10 mg

1 mM	5.2091 mL	26.0457 mL	52.0915 mL
5 mM	1.0418 mL	5.2091 mL	10.4183 mL
10 mM	0.5209 mL	2.6046 mL	5.2091 mL

View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (protect from light). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Molarity Calculator
Dilution Calculator

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

This equation is commonly abbreviated as: C₁V₁ = C₂V₂

Concentration _(start)

Volume _(start)

Concentration _(final)

Volume _(final)

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

Dosage

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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Calculation results:

Working solution concentration: mg/mL

Purity & Documentation

Purity: 95.87%

Select Batch:

Data Sheet (247 KB) SDS (251 KB)

COA (255 KB) HNMR (237 KB) LCMS (88 KB)

Handling Instructions (2659 KB)

Complete Stock Solution Preparation Table

Optional Solvent	Concentration Solvent Mass	1 mg	5 mg	10 mg	25 mg

DMSO	1 mM	5.2091 mL	26.0457 mL	52.0915 mL	130.2287 mL
	5 mM	1.0418 mL	5.2091 mL	10.4183 mL	26.0457 mL
	10 mM	0.5209 mL	2.6046 mL	5.2091 mL	13.0229 mL
	15 mM	0.3473 mL	1.7364 mL	3.4728 mL	8.6819 mL
	20 mM	0.2605 mL	1.3023 mL	2.6046 mL	6.5114 mL
	25 mM	0.2084 mL	1.0418 mL	2.0837 mL	5.2091 mL
	30 mM	0.1736 mL	0.8682 mL	1.7364 mL	4.3410 mL
	40 mM	0.1302 mL	0.6511 mL	1.3023 mL	3.2557 mL
	50 mM	0.1042 mL	0.5209 mL	1.0418 mL	2.6046 mL
	60 mM	0.0868 mL	0.4341 mL	0.8682 mL	2.1705 mL
	80 mM	0.0651 mL	0.3256 mL	0.6511 mL	1.6279 mL
	100 mM	0.0521 mL	0.2605 mL	0.5209 mL	1.3023 mL