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166510

Sigma-Aldrich

1,1′-Diethyl-2,2′-carbocyanine iodide

97%

Synonym(s):

Pinacyanol iodide, Quinaldine blue

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About This Item

Empirical Formula (Hill Notation):
C25H25IN2
CAS Number:
605-91-4
Molecular Weight:
480.38
Beilstein:
4117070
EC Number:
210-099-4
MDL number:
MFCD00011975
UNSPSC Code:
12171500
PubChem Substance ID:
24850168
NACRES:
NA.47

Assay

97%

form

powder

mp

295 °C (dec.) (lit.)

solubility

ethanol: 10 mg/mL

λmax

614 nm

ε (extinction coefficient)

≥180000 at 602-608 nm in ethanol
≥80000 at 560-566 nm in ethanol

application(s)

diagnostic assay manufacturing
hematology
histology

storage temp.

2-8°C

SMILES string

[I-].CCN1\C(=C\C=C\c2ccc3ccccc3[n+]2CC)C=Cc4ccccc14

InChI

1S/C25H25N2.HI/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

QWYZFXLSWMXLDM-UHFFFAOYSA-M

Related Categories

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Statements

H301 + H311 + H331

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

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)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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1,6-Diphenyl-1,3,5-hexatriene 98%

Sigma-Aldrich

D208000

1,6-Diphenyl-1,3,5-hexatriene

Tariq Mahmood et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(39), 12349-12356 (2012-08-22)
The synthesis of a geometrically constrained and near-planar hexacyclic acridinium cyanine dye 9 is reported. When compared to its unlocked and non-fluorescent monomethine cyanine dye analogue 3, this photostable dye emits in the green area of the spectrum with a
Y Iwamoto et al.
Journal of pharmacobio-dynamics, 13(5), 316-320 (1990-05-01)
Photobiological activities of pinacyanol chloride (PC), which is known as a non-intercalating dye, were investigated. Irradiation of PC-sensitized yeast cells in the dark brought about marked decrease of survival and induction of "petites" which are respiration-deficient mutants caused by partial
R Vazquez-Duhalt et al.
Enzyme and microbial technology, 15(11), 936-943 (1993-11-01)
The effect of five water-miscible organic solvents (tetrahydrofuran, N,N-dimethylformamide, acetonitrile, 2-propanol, and methanol) on the oxidation of pinacyanol chloride (Quinaldine Blue) by horse heart cytochrome c was determined. Hydrogen peroxide was used as the oxidant, and a change in catalytic
A Chakrabarti et al.
Indian journal of biochemistry & biophysics, 26(2), 74-79 (1989-04-01)
The acidic capsular polysaccharide isolated from Klebsiella K10 exhibited chromotropic character with respect to induction of metachromasy in the cationic dye pinacyanol chloride (1-ethyl-2-[3-(1-ethyl-2(1H)-quinolylidene)propenyl]quinolinium chloride). Klebsiella K10 polymer consists of hexasaccharide repeating units containing one residue of glucuronic acid along
Raimon Sabaté et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 70(2), 471-476 (2007-10-30)
Pinacyanol (PIN), as other cyanine dyes, has demonstrated a unique ability to form associates such as dimers, and H- and J-aggregates. This association is strongly favoured in water, and even at low dye concentrations, dimers and superior order aggregates are
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