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| PHTHALOCYANINE BLUE NCF | ||
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PRODUCT IDENTIFICATION |
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| CAS NO. | 147-14-8 |
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| EINECS NO. | 205-685-1 | |
| FORMULA | C32H16CuN8 | |
| MOL WT. | 576.08 | |
| H.S. CODE | ||
| TOXICITY | ||
| SYNONYMS | C.I. Pigment Blue 15:4; C.I. 74160; | |
| Copper phthalocyanine; Blue phthalocyanine beta form; Copper(II) phthalocyanine; Copper phthalocyanine blue; Cu-Phthaloblue; Copper tetrabenzoporphyrazine; Tetrabenzo-5,10,15,20-diazaporphyrinephthalocyanine; | ||
| DERIVATION |
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CLASSIFICATION |
Phthalocyanine Blue | |
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PHYSICAL AND CHEMICAL PROPERTIES |
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| PHYSICAL STATE | powder | |
| MELTING POINT | ||
| BOILING POINT | ||
| SPECIFIC GRAVITY | 1.57 | |
| SOLUBILITY IN WATER | Insoluble | |
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PRINTING RESISTANCE |
Light Full Shade (8), Light Tint Shade (7), Water (5), Acid (5), Alkali (5), Paraffin Wax (5), Heat (200 C) | |
| SOLVENT RESISTANCE |
Ethanol (5), Butanol (5), Butyl Acetate (5), M.E.K.(5),
Xylene (4), White Spirit
(5)
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| pH | 6 - 8 | |
| VAPOR DENSITY | ||
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AUTOIGNITION |
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| NFPA RATINGS | ||
| FLASH POINT |
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| STABILITY | Stable under ordinary conditions. | |
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GENERAL DESCRIPTION & APPLICATIONS |
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Phthalocyanine is
a macrocyclic compound, It consists of four isoindole-class
[(C6H4)C2N] units linked by four nitrogen atoms to form a conjugated chain,
which take play in hosting various different metal ions in its centrer. This
structure is Macrocyclic structure shows a striking feature as a colorant like
porphyrins (biopigments) in nature. Phthalocyanine derivatives derived from
the basic compound of (C6H4C2N)4N4 are used as light-fast blue or green
pigments. The hosted metals and substituted groups result in distinct colors;
phthalocyanine (blue-green), copper phthalocyanine (blue), chlorinated copper
phthalocyanine (green), and sulfonated copper phthalocyanine (green). Recently
they are involved in the study of photosensitizer chemistry or metal complex chemistry such
as transition-metal complex catalyst chemistry for uniform polymerization,
luminescence chemistry and spectrophotometric analysis, organic synthesis and
polymerization. Phthalocyanine pigments are used in enamels, linoleum, inks,
plastics, and rubber goods. Photoisomerizable phthalocyanines are used in rewritable CD or DVD printing. Some phthalocyanines such as fluoraluminium phthalocyanine are used in cancer treatment.
Due to pi-electron cloud overlaps, phthalocyanines exhibit semiconductor property. Organic semiconductors have some merits of self radiation, flexibility, light weight, easy fabrication, and low cost. They have been investigated as organic electroluminescence materials for the applications in organic solar cells, biosensitizers and display devices such as OLED(Organic Light Emiting Diode), OTFT(Organic Thin Film Transistor), Wearable Display, and e-paper. |
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| SALES SPECIFICATION | ||
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COLOR SHADE |
Similar to the standard | |
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STRENGTH |
> 100.0% | |
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MOISTURE |
1.0% max | |
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OIL ABSORBTION |
45 - 55 (g/100g) | |
| TRANSPORTATION | ||
| PACKING | ||
| HAZARD CLASS | ||
| UN NO. | ||
| ADDITIONAL CAS RN | ||
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10482-39-0; 11097-56-6; 11129-84-3; 12767-67-8; 34567-54-9; 37223-81-7; 39378-75-1; 39473-10-4; 51331-32-9; 53028-77-6; 53802-06-5; 55819-49-3; 57425-52-2; 57916-96-8; 59518-91-1; 59966-88-0; 60880-51-5; 60937-79-3; 61489-66-5; 61489-77-8; 61537-10-8; 64333-57-9; 66121-19-5; 69431-77-2; 78170-27-1; 78413-59-9; 85255-95-4; 90452-20-3; 92909-14-3; 95660-31-4; 95917-74-1; 96024-35-0; 109675-77-6; 109766-95-2; 115284-42-9; 158853-86-2; 172826-46-9; 177529-54-3; 184007-78-1; 213190-86-4; |
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