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Pigment Red 149, also known as a perylenediimide dye, is a red powder with a yellowish shade. It is characterized by its heat resistance of at least 300°C, light fastness rating of 7-8, and good resistance to acids and alkalis with a rating of 5. Additionally, it has a fastness to bleeding rating of 5, oil absorption of 40-50%, a specific surface area of 28m2/g, a density of 1.50 g/cm3, and a maximum residue on 80 mesh of 5.0%. It also has a water solubility of 1.0% max and a volatile content at 105 °C of 1.0% max. With a tinting strength of 100-105%, Pigment Red 149 is a highly effective pigment.

4948-15-6

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4948-15-6 Usage

Uses

Used in Lithium-ion Batteries:
Pigment Red 149 is used as a cost-efficient cathode material for lithium-ion batteries, contributing to the development of more affordable and efficient energy storage solutions.
Used in Bioprobes for Biotinylated Antibodies:
Pigment Red 149 is used as a doping agent for poly(styrene-co-maleimide) nanoparticles, which are employed as bioprobes for biotinylated antibodies. This application takes advantage of the pigment's properties to enhance the functionality and performance of these bioprobes in various biological and medical applications.

Flammability and Explosibility

Notclassified

TEST ITEMS

SPECIFICATION

HEAT RESISTANCE

300 °C min

LIGHT FASTNESS

7-8

ACID RESISTANCE

5

ALKALI RESISTANCE

5

FASTNESS TO BLEEDING

5

OIL ABSORPTION

40-50%

SPECIFIC SURFACE

28m 2 /g

DENSITY

1.50 g/cm 3

RESIDUE ON 80 MESH

5.0% max

VOLATITE 105 °C

1.0% max

Check Digit Verification of cas no

The CAS Registry Mumber 4948-15-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,4 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4948-15:
(6*4)+(5*9)+(4*4)+(3*8)+(2*1)+(1*5)=116
116 % 10 = 6
So 4948-15-6 is a valid CAS Registry Number.
InChI:InChI=1/C40H26N2O4/c1-19-13-20(2)16-23(15-19)41-37(43)29-9-5-25-27-7-11-31-36-32(40(46)42(39(31)45)24-17-21(3)14-22(4)18-24)12-8-28(34(27)36)26-6-10-30(38(41)44)35(29)33(25)26/h5-18H,1-4H3

4948-15-6Downstream Products

4948-15-6Relevant academic research and scientific papers

A perylene pigment preparation method

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Paragraph 0031; 0032, (2019/04/11)

The present invention provides a perylene pigment preparation method, is to adopt the N - substituted - 1, 8 - naphthalene imide as the starting material, in order to N - methyl imidazole with DBU or DBN N - methyl imidazole with the mixed solvent as reaction medium, sodium alcoholate or polysiloxane as catalyst, through 130 - 170 °C reaction 3 - 10 hours, after the reaction, the reaction system cooling, concentrated under reduced pressure, recycling the reaction solvent, collects the product make the perylene pigment. Preparation of perylene pigment coloring high, bright color, good dispersibility, and this process is simple, time consuming and short, the reaction temperature is low, to reduce the use of strong alkali and concentrated sulfuric acid, the production cost is reduced, the reduction of the waste water and the solid waste discharge.

[...] derivatives and their use

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Paragraph 0070; 0071; 0072; 0073; 0074; 0075; 0076, (2016/11/21)

The invention relates to an N,N'-dimethyl-3,4,9,10-perylenetetracarboxylic diimide derivative and application thereof. The N,N'-dimethyl-3,4,9,10-perylenetetracarboxylic diimide derivative refers to the compound shown as a formula II in the specification or salts thereof. The designed and synthesized N,N'-dimethyl-3,4,9,10-perylenetetracarboxylic diimide derivative can be used for preparing perylene pigments such as C.I.pigment red 149. The perylene pigment prepared by the N,N'-dimethyl-3,4,9,10-perylenetetracarboxylic diimide derivative disclosed by the invention has large specific surface area and narrow particle size distribution.

Soluble Perylene Fluorescent Dyes with High Photostability

Rademacher, Andreas,Maerkle, Suse,Langhals, Heinz

, p. 2927 - 2934 (2007/10/02)

The preparation of several 3,4,9,10-perylenebis(dicarboximides) 1 is described and their photostability quantitatively determined and discussed.It is shown, that substitution of the insoluble perylene dye pigments with tert-butyl groups causes solubility in organic solvents leading to high quantum yields of these dyes.

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