BCIPP-RO

BCIP

Manufacturer: Sigma Aldrich

CAS Number: 6578-06-9

Synonym(S): 5-Bromo-4-chloro-3-indolyl phosphate p-toluidine salt, BCIP® p-toluidine salt, X-phosphate p-toluidine salt

Select a Size

Pack Size SKU Availability Price
250 MG BCIPP-RO-250-MG In Stock ₹ 17,060.20
1 G BCIPP-RO-1-G In Stock ₹ 53,313.13

BCIPP-RO - 250 MG

₹ 17,060.20

In Stock

Quantity

1

Base Price: ₹ 17,060.20

GST (18%): ₹ 3,070.836

Total Price: ₹ 20,131.036

description

5-bromo-4-chloro-3-indolyl-phosphate, 4-toluidine salt

Quality Level

100

Assay

99% (HPLC)

form

powder

mol wt

Mr 326.44 (BCIP)Mr 433.6 (BCIP toluidine salt)

packaging

pkg of 1 g (11585002001)pkg of 250 mg (10760994001)

manufacturer/tradename

Roche

solubility

DMF: soluble

storage temp.

2-8°C

SMILES string

Cc1ccc(N)cc1.OP(O)(=O)Oc2c[nH]c3ccc(Br)c(Cl)c23

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Description

  • General description: BCIP serves as substrate for alkaline phosphatase. The reaction product has a blue color and is insoluble in water. The blue color can be visually detected.
  • Application: For the colorimetric detection of alkaline phosphatase-labeled molecules, 5-Bromo-4-chloro-3-indolyl phosphate (BCIP) and Nitro Blue Tetrazolium (NBT) are available. The BCIP/NBT substrate system is versatile and functions in a variety of applications, including Northern Southern, and Western blotting, in situ hybridization, and immunohistochemistry. BCIP is provided in two salt forms: the disodium salt which is soluble in water and the p-toluidine form which is soluble in dimethylformamide. These salt forms may be used to prepare a stock solution that in combination with NBT and a reaction buffer, form a substrate solution for alkaline phosphatase. This substrate system, when incubated with alkaline phosphatase, produces an insoluble NBT diformazan product that is easily observable with its purple color. For added convenience, a mixture of BCIP and NBT is provided in an easily dissolvable tablet form or as a ready-to-use liquid.
  • Quality: Performance test: incubation with AP
  • Substrates: Histochemical substrate for alkaline phosphatase.
  • Analysis Note: Absorption: Absorption maximum in the visible light is not determined.
  • Other Notes: For life science research only. Not for use in diagnostic procedures.
  • Legal Information: BCIP is a registered trademark of Merck KGaA, Darmstadt, Germany

SAFETY INFORMATION

Pictograms

GHS07

Signal Word

Warning

Hazard Statements

H312 - H315 - H319 - H335

Precautionary Statements

P261 - P264 - P280 - P302 + P352 + P312 - P304 + P340 + P312 - P337 + P313

Hazard Classifications

Acute Tox. 4 Dermal - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

136.4 °F

Flash Point(C)

58 °C

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description:
5-bromo-4-chloro-3-indolyl-phosphate, 4-toluidine salt

Quality Level:
100

Assay:
99% (HPLC)

form:
powder

mol wt:
Mr 326.44 (BCIP)Mr 433.6 (BCIP toluidine salt)

packaging:
pkg of 1 g (11585002001)pkg of 250 mg (10760994001)

manufacturer/tradename:
Roche

solubility:
DMF: soluble

storage temp.:
2-8°C

SMILES string:
Cc1ccc(N)cc1.OP(O)(=O)Oc2c[nH]c3ccc(Br)c(Cl)c23

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solubility:
95% ethanol: <1 mg/mL at 20 °CDMSO: <1 mg/mL at 20 °CH2O: <1 mg/mL at 20 °Cacetone: 1-10 mg/mL at 20 °Cmethanol: <1 mg/mL at 20 °Ctoluene: 5-10 mg/mL at 20 °C

storage temp.:
2-8°C

SMILES string:
c1ccc2cc-3c(cc2c1)-c4cccc5cccc-3c45

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JRC

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__

storage temp.:
2-8°C

SMILES string:
c1ccc2c(c1)c3cccc4ccc5cccc2c5c34