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102185-33-1 molecular structure
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disodium 5-bromo-4-chloro-1H-indol-3-yl phosphate

ChemBase ID: 102949
Molecular Formular: C8H4BrClNNa2O4P
Molecular Mass: 370.431961
Monoisotopic Mass: 368.85452249
SMILES and InChIs

SMILES:
[Na+].[Na+].[O-]P(=O)([O-])Oc1c[nH]c2c1c(Cl)c(Br)cc2
Canonical SMILES:
Clc1c(Br)ccc2c1c(c[nH]2)OP(=O)([O-])[O-].[Na+].[Na+]
InChI:
InChI=1S/C8H6BrClNO4P.2Na/c9-4-1-2-5-7(8(4)10)6(3-11-5)15-16(12,13)14;;/h1-3,11H,(H2,12,13,14);;/q;2*+1/p-2
InChIKey:
OAZUOCJOEUNDEK-UHFFFAOYSA-L

Cite this record

CBID:102949 http://www.chembase.cn/molecule-102949.html

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NAMES AND DATABASE IDS

NAMES AND DATABASE IDS

Names Database IDs
IUPAC name
disodium 5-bromo-4-chloro-1H-indol-3-yl phosphate
IUPAC Traditional name
dipotassium 5-bromo-4-chloro-1H-indol-3-yl phosphate
disodium 5-bromo-4-chloro-1H-indol-3-yl phosphate
Synonyms
BCIP
X-phosphate
5-BROMO-4-CHLORO-3-INDOLYL PHOSPHATE DISODIUM SALT
BCIP®
X-phosphate disodium salt
5-Bromo-4-chloro-3-indolyl phosphate disodium salt
5-溴-4-氯-3-吲哚磷酸 二钠盐
CAS Number
102185-33-1
MDL Number
MFCD00036757
PubChem SID
162089603
PubChem CID
6097197

DATA SOURCES

DATA SOURCES

All Sources Commercial Sources Non-commercial Sources
Data Source Data ID
PubChem 6097197 external link

CALCULATED PROPERTIES

CALCULATED PROPERTIES

JChem
Acid pKa 1.726015  H Acceptors
H Donor LogD (pH = 5.5) 0.10124553 
LogD (pH = 7.4) -0.6621499  Log P 2.4873745 
Molar Refractivity 60.1825 cm3 Polarizability 25.167912 Å3
Polar Surface Area 88.21 Å2 Rotatable Bonds
Lipinski's Rule of Five true 

PROPERTIES

PROPERTIES

Physical Property Safety Information Product Information Bioassay(PubChem)
Solubility
DMF: insoluble expand Show data source
H2O: soluble20 mg/mL expand Show data source
Apperance
powder expand Show data source
Melting Point
> 300°C expand Show data source
Storage Condition
0°C, Desiccate, Protect from light expand Show data source
-20°C, Desiccate, Protect from light expand Show data source
MSDS Link
Download expand Show data source
Download expand Show data source
Download expand Show data source
German water hazard class
3 expand Show data source
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter expand Show data source
Storage Temperature
-20°C expand Show data source
Purity
>98% expand Show data source
≥98% expand Show data source
≥98.0% (HPLC) expand Show data source
99% expand Show data source
Grade
for molecular biology expand Show data source
Certificate of Analysis
Download expand Show data source
Download expand Show data source
Foreign Activity
Protease, none detected expand Show data source
Linear Formula
C8H4BrClNO4P · 2Na expand Show data source

DETAILS

DETAILS

MP Biomedicals MP Biomedicals Sigma Aldrich Sigma Aldrich
MP Biomedicals - 02150042 external link
Substrate for alkaline phosphatase
Purity: 99%
MP Biomedicals - 02193989 external link
Molecular Biology Reagent
Disodium Salt
Purity: >98%
Chromogenic substrate for alkaline phosphatase in ELISA.
Sigma Aldrich - B1026 external link
Substrates
Histochemical substrate for alkaline phosphatase.
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.
法律信息
BCIP 注册商标 Sigma-Aldrich Co. LLC
Sigma Aldrich - 16668 external link
Other Notes
For visualizing antigenic proteins immobilized on nitrocellulose paper1,2
Substrates
Histochemical substrate for alkaline phosphatase.
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.
Legal Information
BCIP is a registered trademark of Sigma-Aldrich Co. LLC

REFERENCES

REFERENCES

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PATENTS

PATENTS

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