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3,3'-Diethylthiacarbocyanine iodide

Catalog Number
ACM905975-2
CAS Number
905-97-5
Product Name
3,3'-Diethylthiacarbocyanine iodide
Structure
Category
Cyanine Dyes, Squarylium Dyes; Other Materials
Synonyms
3-Ethyl-2-[3-[3-ethyl-2(3H)-benzothiazolylidene]-1-propenyl]benzothiazolium Iodide DiSC2(3)
Description
Alfa Chemistry offers high-purity 3,3'-Diethylthiacarbocyanine Iodide products for various research purposes. Please contact us by email if you do not find the specification you are looking for on this page.
IUPAC Name
(2Z)-3-ethyl-2-[(E)-3-(3-ethyl-1,3-benzothiazol-3-ium-2-yl)prop-2-enylidene]-1,3-benzothiazole;iodide
Molecular Weight
492.44
Molecular Formula
C21H21IN2S2
Canonical SMILES
CCN1C2=CC=CC=C2SC1=CC=CC3=[N+](C4=CC=CC=C4S3)CC.[I-]
InChI
InChI=1S/C21H21N2S2.HI/c1-3-22-16-10-5-7-12-18(16)24-20(22)14-9-15-21-23(4-2)17-11-6-8-13-19(17)25-21;/h5-15H,3-4H2,1-2H3;1H/q+1;/p-1
InChI Key
VZBILKJHDPEENF-UHFFFAOYSA-M
Melting Point
268 °C
Purity
>98.0%(HPLC)(N)
Appearance
Amber to Brown to Dark green powder to crystal
Application
Cyanine dyes are useful for silver photography, and optical recording media by laser sensitivity. Water-soluble cyanine dyes are usable as fluorescent probes in biochemical research.
Complexity
474
Covalently-Bonded Unit Count
2
Exact Mass
492.01909g/mol
Features And Benefits
Cyanine dyes contain some N-heterocycles on both sides of the polymethine structure. The N-heterocycle on the one side is a cationic ammonium with an electron-withdrawing effect, and the other N-heterocycle is a tertiary amine with an electron-donating effect. Accordingly, cyanine dyes show the light absorption of a charge transfer through the central polymethine structure.
Formal Charge
0
Heavy Atom Count
26
MDL Number
MFCD00011956
MeSH Entry Terms
3,3'-diethylthiacarbocyanine iodide
Monoisotopic Mass
492.01909g/mol
Rotatable Bond Count
4
Storage Conditions
Store at room temperature and dry
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