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Emil Wich

Sandoz Color & Chemicals


Pigments Department
East Hanover, New Jersey 07936

The Colour lndex

An extensive international compilation of the structure in 1894, a second edition of the translation in 1904 and a
and properties of dyes and pigments, as well as a system reprint in 1908.
of numbering these materials, the Colour Index is a po- Development of the British dye industry necessitated by
tentially valuable tool for all users of colorants. For lack the 1914-18 war again brought to mind the need for a
offamiliarity it is not as widely used as it should be. This current survey of available commercial dyes and this was
paper describes the Colour lndex and how to use it. undertaken by the Society of Dyers and Colourists. This
resulted in the publishing of the first Colour Index in 1924
and a Supplement in 1928 with F. M. Rowe as the Editor.
History
The example of Schultz and Julius was followed in ar-
Prior to the discovery of Mauve and the founding of the coal ranging the dyes according to their chemical constitution.
tar industry by Perkin in 1856, the number of colorants It became apparent that frequent supplements would be
available for use in dyeing and manufacturing processes was required to keep the Colour Index up to date but the
very limited. Other workers were encouraged by this dis- worldwide economic depression of the early 1930’s pre-
covery to produce new coloring matters, and the increase vented this. In the late 1930’s consideration was given to
in the number which became available soon created the updating the current index, but the outbreak of the war in
need for a reference book. 1939 prevented any further work.
This need was first met by J. W. Slater who compiled The At the termination of the war in 1945, the Society of
Manual of Colors and Dyewares published in London in Dyers and Colourists took up the work again and asked the
1870 with a second edition in 1882. Colorants were listed assistance of the American Association of Textile Chemists
strictly in alphabetical order and the same system was fol- and Colorists, who readily accepted. Review of the format
lowed by G . H. Hurst in the Dictionary of the Coal Tar of the Colour Index disclosed that while listing by chemical
Colours, also published in London in 1892, with a second constitution was desired by most color chemists, it was by
edition in 1896, and by C. Rawson, W. M. Gardner and W. no means the best arrangement for users of colorants since
F. Laycock in their Dictionary of Dyes, Mordants and it made no provision for listing dyes whose constitution was
Other Compounds used in Dyeing and Calico Printing, unknown or had not been disclosed. As a result it was de-
released in 1901 and again in 1905 and 1926. cided to divide the Colour Index into two parts: one part
I n 1885 the need existed for a more systematic method (Part I ) to contain the colorants grouped according to their
for listing dyes and pigments according to their hues ar- recognized usage categories, the dyes or pigments them-
ranged in spectral order. This was done by W. R. Rich- selves being arranged in spectral hue order, and the second
ardson in his A Classijkation of the Coal Tar Colours part (Part 11) to contain the colorants arranged according
giving their commercial names, chemical nomenclature, and to their chemical constitutions. Each colorant in Part I was
chemical formulae. given a usage number, e.g., C. I. Acid Yellow 1, and each
This was followed in 1888 by Tabellarische Ubersicht constitution in Part I1 a five-digit number, e.g., C. I. 10316,
der im ~andelbe~ndlichenkunstlicherOrganischen which made the necessary cross-referencing very simple.
Farbstoffe compiled in Germany by G. Schultz and P. It was also decided to have a third part (Part 111) to consist
Julius, classifying the colorants solely by chemical structure. essentially of an alphabetical listing of commercial names
This was the best publication to date and remained the together with the Part I and Part I1 numbers. This second
standard text on the subject for forty years. Seven editions edition of the Colour Zndex was published in 1956, Part I
were published between 1888 and 1939. An English consisting of two volumes and Parts I1 and I11 of one volume
translation of the second edition was published in England each. It was intended to keep the Index up to date by issuing
supplementary volumes as occasion demanded, and the first
supplement to the second edition was published in 1963.
0 1977 by John Wiley & Sons, Inc. Since the Colour Index had now been established as the

Volume 2, Number 2, Summer 1977 77


leading work in the field of colorant classification, is the ican dyes, and for dyes from all countries in Central and
most valuable reference for manufacturers and users, and South America, excluding British possessions, are directed
is officially recognized by departments of many govern- to the Colour Zndex Editorial Committee of the American
ments for both scientific and commercial purposes, the Association of Textile Chemists and Colorists, a subcom-
demand for the second edition led to its going out of print mittee of the AATCC Publications Committee. These re-
long before it was originally expected. The need for a quests are forwarded to the Colour Index Editorial Board
completely revised and enlarged third edition was made of the Society of Dyers and Colourists in England. Requests
evident by the increase in the number of generic names of for names from all other countries are referred directly to
individual dyes and pigments from approximately 6,000 in the English Board, who alone assigns the names. The Cof-
the second edition to approximately 8,000 in the second our Index is published by the Society of Dyers and Col-
edition and supplement, an increase of 33% in seven ourists with acknowledgment to the American Association
years. of Textile Chemists and Colourists for its contribution of
technical information. The AATCC Editorial Committee
sees all the additions and amendments and corrections of
Third Edition of the Colour Index
errors at several stages.
The third and latest edition of the Colour Index, published In order to keep the Colour Index up to date, not only will
in 197 I , consists of five volumes. Volumes 1-3 contain, in the additions and amendments be issued quarterly, but Vol.
labular form, the technical information for each C. I. 5 , which contains the commercial names indexed alpha-
Generic Name, and Vol. 4 gives the structural formula betically and under the C. 1. Generic Names, will be
where known or disclosed, together with an outline of the brought up to date and issued in revised form at possibly
method of preparation and literature references. The entries five-year intervals.
in Vol. 1-3 and Vol. 4 are crossreferenced. Volume 5 con- Between the date of publication of the third edition of the
tains lists of manufacturers and code letters allocated to Colour Zndex (November 197 1) and July 1974, there were
them, the C. 1. Generic Names Index, and an alphabetical twelve issues of “Additions and Amendments.” (Products
Commercial Names Index. The format of the third edition no longer available from a given manufacturer were deleted
is described in Table I. from the listings.) All of this information has been expanded
A reference book of this type can never be final, and and consolidated into two volumes and published in 1975
additions and amendments as well as corrections of errors as: Revised Vol. 5 (updated replacement for current Vol.
become necessary. Additions are handled in the following 5) and Supplement-Vol. 6 (supplementary information to
way. Requests for Colour Index generic names for Amer- Vols. 1-4 contained in Additions and Amendments 1 -
12).
TABLE I. Format of the third edition of the Colouf Index.

Vol. Generic Name of Colorant Class Number of Listings


How to Use the Colour Index

1783
When dyes are bought and sold, the user may be inter-
1 AcidDyes
Azoic Coloring Matters ested in finding a substitute or alternate source of supply,
Coupling Components 113 particularly if it is in short supply. A salesman may wish to
Diazo Components 140
373
know which of his products to offer as a replacement for one
Basic Dyes
2 Developers 26 now being used by his customer. A manufacturer may wish
Direct Dyes 1319 to recommend a dye or pigment suitable as a colorant for
Disperse Dyes 752
269
his product and may not favor a particular dye manufac-
Fluorescent Brighteners
Food Dyes 56 turer. This is accomplished through the listing of dyes or
Ingrain Dyes 22 pigments by Colour Index generic name. By definition, the
Leather Dyess -
C. 1. Name and Number are the generic name and number
3 Mordant Dyes 598
Natural Dyes 93 assigned to a given product according to its general usage,
Oxidation Bases 35 e.g., acid dyes, basic dyes, solvent dyes, pigments, etc.
Pigments 633
526
For example, if one knows the trade name of a solvent-
Reactive Dyes
Reducing Agents 13 soluble dye used for coloring plastics and wishes to find the
Solvent Dyes 582 Colour Index Number and the manufacturer, he would
Sulphur Dyes 180
17
refer to the alphabetical product listing in Vol. 5 for that
Condense Sulfur Dyes
Vat Dyes 422 dye. Taking Calco Oil Red D as an example, p. 5392 of
Total 7952b revised Vol. 5 shows ACY as the code letters for the man-
4 Chemical Constitutions ufacturer, C. I. Solvent Red 24 as the generic Colour Index
Intermediate Compounds
5 Manufactures and Code Name Name and Number, and C. I. 26105 as the C. I. Constitu-
Generic Index tion Number. The identity of the manufacturer can be
Alphabetical Index verified by referring to the forepart of Vol. 5 which indicates
Use category for previously listed dyes. ACY as being American Cyanamid. If one wishes to find
Including additions and Amendments Nos. 1-8. other manufacturers of the same product, he would refer

70 COLOR research and application


C.I. Solvent Red 24-37

FASTNESS

Hue us.ux
5 5:

24 26105 I D ~ s ~ r o Red- Good 184- 120 Insol Unalt Unalt Hydrocarbon r o l ~ e n f i ,


Bluish Red 185 (mineral oil) oils. fats and n a c s in
(recryst) shoe and floor polisher
A'otr: Some brands are mixtures of homologous and/or i w - in petrol, oils and
rneric dyes (e.g. with C.I. Solvent Re& 27 and 23) and the greases, \vwd stains.
fastnesn and solubility prapertiea vary accordingly soap, polyrr).rer.e. N C
CF and oily resin 13:
qucn and varnishes.
Cellulose acecate and
acrylic resins
Aka used as an indlcarol

SOLUBILITY IN
CJ.
-=- 1
*x
Y .
9: 2 - " - a
c"g x,
z -
$7 -5: $!
5 +, 9 . 5 ; solvent
g$9 =s.2 $=-k
; *:A3
xg
; k'd B .:z
Eg 2 Red
<-
2
*
=
c
i) ": z z z 0 3 z; 9'5 E 2% g g

0 !5- 0 0.12- - SS 0.02- - 0-38- - - 0.08- 0.26- - VS S 0.2-5 0.03- - a


J ? 3 1 1 1 5 1

to the C. I. Generic Names Index, also in revised Vol. 5, facturer, C. I. Pigment Blue 15 as the generic Colour Index
where the listing for C. I. Solvent Red 24 on p. 5273 shows name and number, and C. I. 74160 as the C. I. Constitution
that NAC (National Aniline), GAF (General Aniline Number. Some Colour Index numbers, particularly for the
Corporation), and SDH (Hilton Davis) are among the pigments, are divided in subgroups to indicate different
many listed as being manufacturers of the same or similar physical properties or different salts of a colorant having
products, with the trade name indicated for each manu- the same basic chemical constitution. Different physical
facturer. forms of a given dye or pigment are also listed under the
If technical information for this product is desired, the same C. I. number. For example, aqueous dispersions,
reader can refer top. 3594 and 3595 of Vol. 3 to locate the plastic chips or concentrates, flushings in vehicles for
data shown in Fig. 1 on chemical class, hue, fastness, usage, printing inks and in plasticizers for plastics, dry toners, and
and solubility in various solvents. The chemical constitution presscake of phthalocyanine blue are all listed as C. I.
of this product is given on p. 4227 of Vol. 4, reproduced in Pigment Blue 15. In this case, C. I. Pigment Blue 15 is the
part in Fig. 2, as the product obtained by coupling 4-o-to- alpha-type red-shade crystallizing, 15:1 the alpha-type
lylazo-o-toluidine with 2-naphthol. By definition, the C. 1. red-shade nonflocculating, 15:3 the beta-type green-shade,
Constitution Number (five-digit number) is the number for and 15:4 the beta-type green-shade nonflocculating pig-
a given product according to its chemical classification,e.g., ment. In the case of Permanent Red 2B (C. I. Pigment Red
monoazo, disazo, triphenylmethane, anthraquinone, etc. 48), however, Pigment Red 48 is the sodium salt, 48:l the
If the trade name of a pigment is known, the same pro- barium salt, 48:2 the calcium salt, 48:3 the strontium salt,
cedure is followed to determine the information desired. The and 48:4 the manganese salt. These subgroups are of great
entry for Monastral Fast Blue BF, as indicated on p. 5618 assistance to the end user in selecting colorants for a specific
of Revised Volume 5, lists DUP (du Pont) as the manu- purpose.

FIAT 764 - Sudan Red BB I

Soluble in ethanol and one


Vtry .oluhlc in b e m e
HISO, conc. - bluish gmn;on dilution - red ppt.

FIG. 2. Chemical structure of C. I. Solvent Red 24, found on p. 4227 of Vol. 4 of the Colour Index.

Vdunw 2, Number 2, Summer 1977 79


~- ~~

74160 C.1. Pigment Blue 15 (Hngbt Mvr) D~JCOUWWI - Dandridye, Drerher and 'I'homar 1928
Scottish Dyes, BP 322169
I.C.I.. BP 41O814, 464126, 476243
American Cynnnmid Co., USP 2460779. 2460783
Du Pont, USP 2452606
Montecatini. BP 503029
Roberta Chemical Co., USP 2471794
Sherwin-Williams Co., BP 640576, 648688
\
c=s
. " s\- c/ Standard Ultramarine Co., USP 2469663
Wiswall, USP 2486351
BIOS 960, 33 - Heliogen Blue B
FD 2696/46 (PB 74220)
FIAT 1309, 8; 1313, 111, 273-385 - Heliogen Blue B
Dent & Linstead, JCS (1934). 1027
Dent, Linstead & Lowe, JCS (1934). 1033
Vanous methods, e.g. - Barren, Dent & Lidstead, JCS (1936), 1719
(1) Heat phthalonitrile with cupmus chloride at 180-200"C Dahlen, Ind. Eng. C h .(1939). 839
de Diesbach, et al., Heir. Chim. Acto. 10 (192i). 886
(2) Heat phthalic anhydride, phthalimide or phthalamide with a Haddock, JSDC. 61 (1945). 68; Rescorch. l(1948). 685
copper salt and urea, cyanoguanidine or p-toluenesulfonamide and Hamm & Norman, J . Appi. Phys. 19 (19+8). 109;
cuprous (or cupric) chloride in prracnce of ammonium molybdate or I.C.I., JSDC, 52 (1936), 22
arsenic oxide (phthalic anhydridelurea process) Stadlinger, Chon. 2.60 (19361, 315
(3) Impregnate the fibre with 1,3-diiminoisoindoline and a copper vop Susich, FIAT 1313. 111, 446
palr and heat in presence of reducing agents to form copper hthalo- Tarantino. Stubbs. Cooke & \Ielsheimer, C a h Trrh. mi.
cyanine in sifu. T h i s pncumr is Phthalogen Brilliant Blue I F k (C.I. No. 902 (1951)
Ingrain Blue 2); when a nickel salt U used. nickel phthalocyanine is Chinolfi, Ind. vmricr (Milon).9 (1955\, 181
formed in situ yielding a nore greenish blue than the bright blue dyeing Biplow & Perkins, Allen, L&r, SVO. 658
ohtamed ,with a copper uIt-FBy. BP 698039. 698049. 698070; Bau-
mann. Bienert. R a u h , Vollrnann and Wolf, Angew. C'hcm. 68 (1956), Soluble in 98% H,SO,
133-150; F. Cund. J.S.D.C.. 76 (1960) 151-158 Inaoluble in wuter. alcohol and hvdnrarhnns
HaSOI conc. -olive dlution: on dilution - blur pm-ipituitc

FIG. 3. Chemical structure and related information on C. I. Pigment Blue 15, found on p. 4618 of Vol. 4 of the CoIour Index.

Continuing with C. I. Pigment Blue 15, under the generic intentionally to indicate a brighter or duller shade, or a
names listing on p. 5235-6 of Revised Vol. 5 the various shade shifted from yellow to redder, green to bluer, etc., by
manufacturers of this product are listed. For technical in- the addition of another intermediate during the course of
formation one must refer to Vol. 3, p. 3344-5, and for the manufacture. These dissimilar and chemically different
chemical constitution, Vol. 4, p. 46 18 (Fig. 3). This figure types have been classified under the same C. I. name and
illustrates the wealth of background information provided Constitution Number, the justification being that the
in the Colour Index. Constitution Number shows the major component cor-
Other technical information is found in the Colour Index rectly.
which may be of interest in solving certain problems. If one With this in mind, most buyers and users of dyes and
has a colorant which has performed successfully in his pigments know that small differences can and do exist
product and he wishes to find other colorants of the same among various samples that have the same C. I. name, and
general chemical structure, this information can be located that samples of products claimed to be the same C. I. name
in the Colour Index. must and should be evaluated in their own particular end
In the case of C. I. Solvent Red 24, C. I. 26105, previously use product to determine any variations.
referred to as having the general chemical classification of
a disazo dye, by referring to the section on those dyes in the Conclusions
Colour Index, p. 4225 of Vol. 4, it is noted that there are The usefulness of the Colour Index as a reference and aid
18 dyes in the series C. 1.26000-C. I. 26150, dyes without to the buyer, user, and the salesman is well established. The
-COOH, -SO,H, or -S02NHz salt forming groups. This U. S. Tariff Commission also makes use of the Colour
could lead by crossreference to the selection of other dyes Index generic names in reporting the volume of dyes and
for a given end use application. In the case of C. I. Pigment pigments manufactured, sold, or imported in its annual
Blue 15, C. I. 74160, by referring to the section on statistical report. With the cooperation of the various
phthalocyanine dyes and pigments on p. 4617 of Vol. 4 of manufacturers and careful editing of information by the
the Colour Index, additional information is found con- Editorial and Publication Committees, the Colour Index
cerning the general classification of phthalocyanine dyes can be made even more useful in the future.
and pigments. The Colour Index (3rd ed., revised) is published by the
The fact that most dyes (but, in general, not pigments, Society of Dyers and Colourists, P. 0. Box 244, Perkin
although there are some) are mixtures even though they are House, 82 Grattan Road, Bradford, Yorkshire BDl 2JB,
classified under a single C . 1. Name and Constitution England (Vols. 1-4, 1971; Vols. 5 (revised), 6, 1975). It is
Number, is well known. In some cases, the designation available in the U. S. from American Association of Textile
"similar to" is noted. This variation is attributed to the Chemists and Colorists, P. 0. Box 12215, Research
presence of subsidiary dyes normally formed during man- Triangle Park, N. C. 27709.
ufacture, by the presence of isomers in the intermediates The illustrations in this article are 0 1975 by the Society
and as a result unintentionally present in the finished of Dyers and Colourists and the American Association of
product in some reacted form. Textile Chemists and Colorists (all rights reserved) and are
Variations within a C. I. name, however, may be made reprinted with permission.

80 COLOR research and application

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