5-Brom-4-chlor-3-indolylhydrogen-phosphat-p-toluidin (1:1)
5-bromo-4-chloro-3-indolyl phosphate, p-toluidine salt
Grundinformationen
- CAS
6578-06-9- Standard-SMILES
Cc1ccc(N)cc1.O=P(O)(O)Oc1c[nH]c2ccc(Br)c(Cl)c12- InChIKey
QEIFSLUFHRCVQL-UHFFFAOYSA-N- Summenformel
- C15H15BrClN2O4P
- Durchschnittliche Molmasse
- 433,62 g/mol
- Monoisotopische Masse
- 431,96413337
Überblick
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Namen und Bezeichner
- Bevorzugter Name
- 5-bromo-4-chloro-3-indolyl phosphate, p-toluidine salt
- IUPAC
- (5-bromo-4-chloro-1H-indol-3-yl) dihydrogen phosphate;4-methylaniline
- Lokaler Name
- 5-Brom-4-chlor-3-indolylhydrogen-phosphat-p-toluidin (1:1)
- Englischer Name
- 5-Bromo-4-chloro-3-indolyl phosphate p-toluidine salt
- Summenformel
- C8H6BrClNO4P.C7H9N
- Molmasse
- 433.63
Namen und Synonyme
5-Bromo-4-chloro-3-indolyl phosphate p-toluidine saltDTXSID0064412EINECS 229-506-15-Bromo-4-chloro-3-indolyl phosphate, p-toluidine saltBCIP ptoluidine saltRefChem:533662Xphosphate ptoluidine saltDTXCID00446585Bromo4chloro3indolyl hydrogen phosphate ptoluidine (1:1)1HIndol3ol, 5bromo4chloro, 3(dihydrogen phosphate), compd. with 4methylbenzenamine (1:1)1HIndol3ol, 5bromo4chloro, dihydrogen phosphate (ester), compd. with 4methylbenzenamine (1:1)6578-06-9
Weitere Namen anzeigen
BCIP P-TOLUIDINE SALTBClPBCIP-Tabs9176BCIP P-TOLX-PHOS P-TOLBCIP-TOLUIDINEP-toluidinesaltBCIP P-TOLUIDINE
BCIPp-toluidine 5-bromo-4-chloro-1H-indol-3-yl phosphateMFCD000406365-Bromo-4-chloro-3-indolyl phosphate, p-toluidinesaltAC-37057B12395-Bromo-4-chloro-1H-indol-3-yl phosphate p-toluidine5-Bromo-4-chloro-3-indolyl phosphate p-toluidine salt, tablet
Eigenschaften
Berechnete Struktureigenschaften
- Polarare Oberfläche (TPSA)
- 109 Ų
- H-Brücken-Donoren
- 4
- H-Brücken-Akzeptoren
- 5
- Frei drehbare Bindungen
- 2
- Schwere Atome
- 24
- Formalladung
- 0
- Komplexität
- 377
Experimentelle und physikochemische Eigenschaften
Chemical ClassesNitrogen Compounds -> Indoles
Physical DescriptionSolid; [Sigma-Aldrich MSDS]
Physikochemische Eigenschaften
- Schmelzpunkt
- 194 · 194-195℃
- storage temp.
- -20 °C · -20°C
- Löslichkeit
- 20 mg/mL · DMF: 20 mg/mL
- Aggregatzustand
- tablets
- Farbe
- White to Orange to Green
- 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
- InChIKey
- QEIFSLUFHRCVQL-UHFFFAOYSA-N
- SMILES
- C12C(Cl)=C(C=CC=1NC=C2OP(=O)(O)O)Br.C1(C)C=CC(N)=CC=1
- CAS Datenbank
- 6578 · 6578-06-9(CAS DataBase Reference)
- EPA chemische Informationen
- 1 H-Indol-3-ol, · 1H-Indol-3-ol, 5-bromo-4-chloro-, dihydrogen phosphate (ester), compd. with 4-methylbenzenamine (1:1) (6578-06-9)
Sicherheit und Regulatorisches
Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.
GHS-Klassifizierung
GHS Classification
Warning
H302 (52.2%): Harmful if swallowed [Warning Acute toxicity, oral]
P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P317, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 23 reports by companies from 12 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Hazards SummaryA skin and strong eye irritant; [Sigma-Aldrich MSDS] See p-Toluidine and 5-Bromo-4-chloro-3-indoxyl phosphate.
Hazard Classes and CategoriesAcute Tox. 4 (52.2%)
Sicherheitsdaten
- F
- 3-8-10
- wgk
- 3
- tsca
- TSCA listed
- ridadr
- 2811
- hs_code
- 29339190
- risk_code
- 36/37/38-40
- hazard_code
- Xi
- safety_code
- 26
- hazard_class
- 6.1
- packing_group
- III
- Speicherklasse
- 11 - Combustible Solids
Chemie und Industrie
Anwendungen
VerwendenFor 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.
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Shandong chuangyingchemical Co., Ltd.18853181302 · [email protected]
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