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经验公式(希尔记法):
C25H25IN2
化学文摘社编号:
分子量:
480.38
UNSPSC Code:
12171500
NACRES:
NA.47
PubChem Substance ID:
EC Number:
210-099-4
Beilstein/REAXYS Number:
4117070
MDL number:
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
SMILES string
[I-].CCN1\C(=C\C=C\c2ccc3ccccc3[n+]2CC)C=Cc4ccccc14
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
Quality Level
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral
存储类别
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
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Kausik Manna et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 74(5), 1268-1274 (2009-10-28)
Interaction of pinacyanol chloride (PIN) with pure and binary mixtures of cetyltrimethylammonium bromide (CTAB) and sodium deoxycholate (NaDC) was spectroscopically studied. Interaction of PIN with pure NaDC produced a blue shifted metachromatic band (at approximately 502 nm), which gradually shifted
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
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
Sa'ib J Khouri et al.
Carbohydrate research, 344(13), 1729-1733 (2009-08-12)
The interaction between pinacyanol chloride and sodium alginate or guluronate-rich alginate is found to effect profound changes in the visible absorbance and circular dichroism spectra. Two different types of aggregates are observed depending on the relative dye/alginate concentrations. With a
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
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