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5-Bromo-4-chloro-3-indolyl phosphate p-toluidine salt - for molecular biology,≥99%, high purity , CAS No.6578-06-9

  • for molecular biology
  • ≥99%
Item Number
B113076
Grouped product items
SKUSizeAvailabilityPrice Qty
B113076-100mg
100mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$58.90
B113076-500mg
500mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$265.90
B113076-1g
1g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$334.90

Histochemical alkaline phosphatase substrate.

Basic Description

Synonyms6578-06-9|BCIP|5-Bromo-4-chloro-3-indolyl phosphate p-toluidine salt|BCIP p-toluidine salt|X-phosphate p-toluidine salt|p-toluidine 5-bromo-4-chloro-1H-indol-3-yl phosphate|5-Bromo-4-chloro-1H-indol-3-yl phosphate p-toluidine|5-Bromo-4-chloro-3-indolyl ph
Specifications & Purityfor molecular biology,≥99%
Storage TempStore at -20°C,Argon charged
Shipped InDry ice
Gradefor molecular biology
Product Description

For the colorimetric detection of alkaline phosphatase-labeled molecules, 5-Bromo-4-chloro-3-indoly?l 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.
Histochemical substrate for alkaline phosphatase.

Names and Identifiers

IUPAC Name (5-bromo-4-chloro-1H-indol-3-yl) dihydrogen phosphate;4-methylaniline
INCHI InChI=1S/C8H6BrClNO4P.C7H9N/c9-4-1-2-5-7(8(4)10)6(3-11-5)15-16(12,13)14;1-6-2-4-7(8)5-3-6/h1-3,11H,(H2,12,13,14);2-5H,8H2,1H3
InChi Key QEIFSLUFHRCVQL-UHFFFAOYSA-N
Canonical SMILES CC1=CC=C(C=C1)N.C1=CC(=C(C2=C1NC=C2OP(=O)(O)O)Cl)Br
Isomeric SMILES CC1=CC=C(C=C1)N.C1=CC(=C(C2=C1NC=C2OP(=O)(O)O)Cl)Br
WGK Germany 3
PubChem CID 81059
Molecular Weight 433.62

Certificates

Certificate of Analysis(COA)

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7 results found

Lot NumberCertificate TypeDateItem
K2223165Certificate of AnalysisAug 23, 2024 B113076
K2223206Certificate of AnalysisAug 23, 2024 B113076
K2223207Certificate of AnalysisAug 23, 2024 B113076
B2225276Certificate of AnalysisDec 22, 2023 B113076
B2225279Certificate of AnalysisDec 22, 2023 B113076
B1911019Certificate of AnalysisSep 16, 2022 B113076
B2225312Certificate of AnalysisJan 18, 2022 B113076

Chemical and Physical Properties

Sensitivitylight sensitive,air sensitive,heat sensitive
Melt Point(°C)196-198°C

Safety and Hazards(GHS)

Pictogram(s) GHS07
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

WGK Germany 3

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Solution Calculators