Grundinformationen
- Standard-SMILES
OC[C@H]1O[C@@H](Oc2c[nH]c3ccc(Br)c(Cl)c23)[C@H](O)[C@@H](O)[C@H]1O- InChIKey
OPIFSICVWOWJMJ-AEOCFKNESA-N- Summenformel
- C14H15BrClNO6
- Durchschnittliche Molmasse
- 408,63 g/mol
- Monoisotopische Masse
- 406,97713
Namen und Bezeichner
- Bevorzugter Name
- X-Gal
- IUPAC
- (2S,3R,4S,5R,6R)-2-[(5-bromo-4-chloro-1H-indol-3-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
- Lokaler Name
- 5-Brom-4-chlorindol-3-yl-beta-D-galactopyranosid
- Englischer Name
- 5-Bromo-4-chloro-3-indolyl-beta-D-galactoside
- Summenformel
- C14H15BrClNO6
- Molmasse
- 408.63
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
7240-90-6- PubChem CID
- 65181
- DTXSID
DTXSID901349452- ChEMBL
CHEMBL1242856- ChEBI
CHEBI:75055- UNII
- V595OG374W
- EC Number
- 230-640-8
- Nikkaji
- J212.257J
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 1,2
- Polarare Oberfläche (TPSA)
- 115 Ų
- H-Brücken-Donoren
- 5
- H-Brücken-Akzeptoren
- 6
- Frei drehbare Bindungen
- 3
- Schwere Atome
- 23
- Formalladung
- 0
- Komplexität
- 421
Experimentelle und physikochemische Eigenschaften
Physikochemische Eigenschaften
- Schmelzpunkt
- 230 °C · 230 °C
- Siedepunkt
- 673.9 · 673.9±55.0 °C(Predicted)
- Dichte
- 1.5563 · 1.5563 (rough estimate)
- Brechungsindex
- 1.611 · 1.6110 (estimate)
- storage temp.
- -20 °C · -20°C
- Löslichkeit
- 100 mM · Soluble in 100 mM in DMSO.
- Aggregatzustand
- Powder
- pka
- 12.74 · 12.74±0.70(Predicted)
- Farbe
- White
- Geruch (Odor)
- Odorless
- Merck
- 14 · 14,10074
- BRN
- 1402009 · 1402009
- Stabilität
- Stable. Incompatible with strong oxidizing agents.
- InChI
- 1S/C14H15BrClNO6/c15-5-1-2-6-9(10(5)16)7(3-17-6)22-14-13(21)12(20)11(19)8(4-18)23-14/h1-3,8,11-14,17-21H,4H2/t8-,11+,12+,13-,14-/m1/s1
- InChIKey
- OPIFSICVWOWJMJ-AEOCFKNESA-N
- SMILES
- OC[C@H]1O[C@@H](Oc2c[nH]c3ccc(Br)c(Cl)c23)[C@H](O)[C@@H](O)[C@H]1O
- CAS Datenbank
- 7240 · 7240-90-6(CAS DataBase Reference)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
This chemical does not meet GHS hazard criteria for 20% (2 of 10) of reports.
Warning
H302 (80%): Harmful if swallowed [Warning Acute toxicity, oral];H312 (80%): Harmful in contact with skin [Warning Acute toxicity, dermal];H332 (80%): Harmful if inhaled [Warning Acute toxicity, inhalation]
P261, P264, P270, P271, P280, P301+P317, P302+P352, P304+P340, P317, P321, P330, P362+P364, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 10 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.;Reported as not meeting GHS hazard criteria per 2 of 10 reports by companies.;There are 2 notifications provided by 8 of 10 reports by companies with hazard statement code(s).;Information may vary between notifications depending on impurities, additives, and other factors. The percentage value in parenthesis indicates the notified classification ratio from companies that provide hazard codes. Only hazard codes with percentage values above 10% are shown. For more detailed information, please visit ECHA C&L website.
Gefahrenhinweise
Regulatorische Informationen
Sicherheitsdaten
- F
- 8-10-21
- wgk
- 3
- hs_code
- 29389090
- risk_code
- 36/37/38
- hazard_code
- Xi
- safety_code
- 24/25-37/39-26
- hazard_class
- IRRITANT
- Speicherklasse
- 11 - Combustible Solids
Chemie und Industrie
Pharmakologische Informationen
MeSH Pharmacological Classification
Colorless, endogenous or exogenous pigment precursors that may be transformed by biological mechanisms into colored compounds; used in biochemical assays and in diagnosis as indicators, especially in the form of enzyme substrates. Synonym: chromogens (not to be confused with pigment-synthesizing bacteria also called chromogens).
Verwendung und Herstellung
Anwendungen
VerwendenA substrate for -Galactosidase that is converted by the enzyme into an intense indigo-blue chromophore (615 nm)
Anbieter50 Anbieter
Ergänzende Hinweise
DefinitionChEBI: An indolyl carbohydrate that is the beta-D-galactoside of 3-hydroxy-1H-indole in which the indole moiety is substituted at positions 4 and 5 by chlorine and bromine, respectively. It is used to test for he presence of an enzyme, beta-galactosidase, which cleaved the glycosidic bond to give 5-bromo-4-chloro-3-hydroxy-1H-indole, which immediately dimerises to give an intensely blue product.
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