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Blue caprate

CAT: 0013-GTR19247457-02Size: 50 mgDry Ice: NoHazardous: No
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CAT#:0013-GTR19247457-02Size:50 mg
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Description
Blue caprate is a chromogenic enzyme substrate commonly used to detect lipase activity. Upon hydrolysis by lipase, it produces a blue-violet product. (biosynth:EB04034) .
CAS Number
133950-71-7
Smiles
CCCCCCCCCC (=O) OC1=CNC2=C1C=C (C=C2) Br
Molecular Formula
C18H24BrNO2
Molecular Weight
366.29
Storage Conditions
-20°C
Notes
For research use only.

Chemical Information

5-Bromo-1H-indol-3-yl decanoate

5-bromo-3-indolyl decanoate is an decanoate ester obtained by formal condensation of the carboxy group of decanoic acid with the hydroxy group of 5-bromoindoxyl. It has a role as a chromogenic compound. It is a bromoindole and a decanoate ester. It is functionally related to an indoxyl.

CAS Number133950-71-7
PubChem CID14821427
IUPAC Name(5-bromo-1H-indol-3-yl) decanoate
Molecular FormulaC18H24BrNO2
Molecular Weight366.3
XLogP6.6
Topological Polar Surface Area42.1
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count10
Heavy Atom Count22
Formal Charge0
Complexity337
SMILES
CCCCCCCCCC(=O)OC1=CNC2=C1C=C(C=C2)Br
InChI
InChI=1S/C18H24BrNO2/c1-2-3-4-5-6-7-8-9-18(21)22-17-13-20-16-11-10-14(19)12-15(16)17/h10-13,20H,2-9H2,1H3
InChIKey
MSQDUIOYSURQKS-UHFFFAOYSA-N
Chemical Structure
2D Structure
2D structure of 5-Bromo-1H-indol-3-yl decanoate
CAS: 133950-71-7
CID: 14821427
Formula: C18H24BrNO2
MW: 366.3
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight366.3
XLogP36.6
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count10
Exact Mass365.09904
Monoisotopic Mass365.09904
Topological Polar Surface Area42.1 Ų
Heavy Atom Count22
Formal Charge0
Complexity337
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes