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201715

Sigma-Aldrich

Pinacyanol chloride

Synonym(s):

1,1′-Diethyl-2,2′-carbocyanine chloride, 2,2′-Trimethinequinocyanine chloride, Quinaldine blue

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About This Item

Empirical Formula (Hill Notation):
C25H25ClN2
CAS Number:
Molecular Weight:
388.93
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

form

powder

Quality Level

mp

270 °C (dec.) (lit.)

λmax

560 nm (2nd)
604 nm

ε (extinction coefficient)

≥150000 at 603-609 nm in ethanol at 0.001 g/L
≥65000 at 559-565 nm in ethanol at 0.001 g/L

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

room temp

SMILES string

[Cl-].CCN1C(=C\C=C\c2ccc3ccccc3[n+]2CC)\C=Cc4ccccc14

InChI

1S/C25H25N2.ClH/c1-3-26-22(18-16-20-10-5-7-14-24(20)26)12-9-13-23-19-17-21-11-6-8-15-25(21)27(23)4-2;/h5-19H,3-4H2,1-2H3;1H/q+1;/p-1

InChI key

FVMNARAKYNRZID-UHFFFAOYSA-M

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Biochem/physiol Actions

Pinacyanol chloride (1, 1-diethyl-2, 2-carbocyanine chloride), also known as quinaldine blue or PIN, belongs to the class of symmetric trimethinecyanine dyes. It is widely used as a histological stain. Pinacyanol chloride is used in the study of bacterial polysaccharides. Pinacyanol chloride exposure induces respiratory immunogenicity. PIN has two absorption maximums at 605nm and 550nm, which are known asα and β bands respectively.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Michaela Patila et al.
Sensors (Basel, Switzerland), 16(3), 287-287 (2016-03-02)
Multi-layer graphene oxide-enzyme nanoassemblies were prepared through the multi-point covalent immobilization of laccase from Trametes versicolor (TvL) on functionalized graphene oxide (fGO). The catalytic properties of the fGO-TvL nanoassemblies were found to depend on the number of the graphene oxide-enzyme
Spectral studies on the interaction of pinacyanol chloride with binary
surfactants in aqueous medium
Manna K and Panda A K
Spectrochimica Acta , 74, 1268-1274 (2009)
Ryan J Powell et al.
Applied and environmental microbiology, 80(13), 4042-4050 (2014-04-29)
Alga-derived biofuels are one of the best alternatives for economically replacing liquid fossil fuels with a fungible renewable energy source. Production of fuel from algae is technically feasible but not yet economically viable. Harvest of dilute algal biomass from the
R Nandini et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 75(1), 14-20 (2009-12-01)
The interactions of Acridine Orange with Sodium Alginate and Pinacyanol Chloride with Heparin have been investigated by spectrophotometric method. The polymers induce metachromasy in the dye as evidenced from the considerable blue shift in the absorption maxima of the corresponding
T Yamada et al.
Inorganic chemistry, 39(14), 3049-3056 (2001-02-24)
A variety of lariat ethers were employed to solubilize water-soluble cytochrome c in methanol, in which alcohol, ether, ester, amine, and amide functionalities were attached as cation-ligating side arms to 18-crown-6, 15-crown-5, and 12-crown-4 rings. Among these lariat ethers, the

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