indanthrenen.

/ˈɪndənθriːn/

Forms: Also Indanthren(e.

Etymology: < indo- comb. form² + anth- (in anthra- comb. form) + -ene comb. form.

(a) (With lower-case initial.) Indanthrone, C₂₈H₁₄N₂O₄ (in quot. 1921 used for the oxygen-free parent compound, C₂₈H₁₈N₂: cf. quot. 1920). (b) (Usually with capital initial.) Any of a large and important class of vat dyes derived from or containing indanthrone or other compounds based on the anthraquinone nucleus.Indanthren(e) has been registered as a proprietary term in Great Britain.

ΘΚΠ

the world > matter > chemistry > organic chemistry > organic compounds > [noun] > other organic compounds

xanthide1823

idrialin1838

barégin1863

violantin1866

biguanide1881

turmerol1890

tetrazole1892

oxazolone1899

indanthrene1901

silicone1906

platinum blue1908

hydroxycitronellal1929

haloform1931

octamethylcyclotetrasiloxane1946

organo-siloxane1946

chlorofluorocarbon1947

permethrin1975

CFC1976

the world > matter > colour > colouring > colouring matter > [noun] > dye > types of dyes

pallOE

sanders1329

raddlea1350

nutgallc1450

bark1565

logwood1581

sanders-wood1615

catechu1682

cate1698

cachou1708

valonia1722

India wood1742

cutch1759

alizari1769

standard1808

iron buff1836

colorine1838

acid dye1840

garancin1843

French tub1846

suranji1848

morindin1849

water blue1851

union dye1852

indigo-carmine1855

hernant1858

pigment colour1862

rosaniline1862

rose aniline1862

bezetta1863

bottom1863

acid colour1873

paraphenylenediamine1873

indigo-extract1874

tin-pulp1874

phthalein1875

sightening1875

chrome1876

rose bengal1878

azo-colours1879

azine1887

basic dye1892

chromotrope1893

garance1896

ice colour1896

xylochrome1898

cross-dye1901

indanthrene1901

Lithol1903

vat dye1903

thioindigo1906

para red1907

vat colour1912

vat dyestuff1914

indanthrone1920

ionamine1922

Soledon1924

Solochrome1924

Solacet1938

indigoid1939

thioindigoid1943

fluorol1956

Procion1956

the world > matter > colour > named colours > blue or blueness > blue colouring matter > [noun] > dyes and dyestuffs > other dyes

stone-blue1675

starch blue1742

Saxon blue1753

fig-blue1786

chemic1792

Turkey blue1815

Paris blue1835

Saxony blue1857

soluble blue1879

methylene blue1882

indoin1884

phenylene blue1884

indamine1888

Nile blue1888

gallamine blue1889

neutral blue1889

chrome-blue1892

toluidine blue1898

indanthrene1901

Saxe blue1905

trypan blue1911

mandarin blue1912

1901 Trade Marks Jrnl. 23 Oct. 1063 Indanthrene.

1901 Jrnl. Soc. Dyers & Colourists 17 (facing p. 302) Indanthrene X is a blue paste insoluble in water.

1901 Jrnl. Soc. Dyers & Colourists 17 (facing p. 302) Indanthrene S is a coppery coloured paste which is soluble in hot water.

1903 Jrnl. Chem. Soc. 84 i. 446 The substance ‘A’, of the German Patent 135407,..can be purified by dissolving it in concentrated sulphuric acid and allowing the solution to gradually absorb water; well-formed, blue needles separate which, in the case of ‘Indanthrene C’, have the composition C₂₈H₁₀O₄N₂Br₂, and, in the case of indanthrene itself, the composition C₂₈H₁₂O₄ N₂.

1920 F. A. Mason tr. G. von Georgievics Text-bk. Dye Chem. (ed. 2) 452 Flavanthrone..is sold as Indanthrene Yellow G (B.A.S.F.), Chloranthrene Yellow (B.D.L.), and Caledon Yellow G (Sol.).

1920 F. A. Mason tr. G. von Georgievics Text-bk. Dye Chem. (ed. 2) 449 Indanthrene (or more correctly Indanthrone, which expresses the quinoid character of the compound, whereas the name generally used would correspond to an oxygen-free compound) is a dianthraquinone-dihydroazine.

1921 E. de B. Barnett Anthracene & Anthraquinone xvi. 342 The first cyclic azine of the anthraquinone series to be prepared was trans. bisang.-anthraquinonedihydro azine. This was placed on the market under the name Indanthrene Blue, and the name ‘indanthrene’ has come into general use in the literature. The word ‘indanthrene’, however, is a registered trade name (B.A.S.F.) and is applied to many vat dyes which are not azines. Indanthrene Blue is an anthraquinone derivative and ketonic in structure, and in order to denote its ketonic nature the name should terminate in -one. In the following pages, therefore, the word ‘indanthrone’ is used to denote the ketonic hydroazine, indanthrene (without a capital) being used for the parent, oxygen free hydroazine (trans. bisang.-dihydroanthrazine). Where ‘Indanthrene’ is used as a registered trade name it is spelt with a capital.

1922 Trade Marks Jrnl. 8 Nov. 2019 Indanthren.

1952 K. Venkataraman Chem. Synthetic Dyes II. xxx. 861 With the amalgamation of the German dyemakers into the IG in 1924, Indanthrene was adopted as the group name for vat dyes with the maximum all-round fastness.

1961 S. R. Cockett & K. A. Hilton Dyeing of Cellulosic Fibres i. 13 In 1901, the first anthraquinone vat dye, Indanthrone (Indanthrene Blue B), was discovered by Bohn... This was followed in the same year, and from the same chemist, by Flavanthrone (Indanthrene Yellow G) and many other variations.

1971 R. L. M. Allen Colour Chem. x. 163 If hydroxyl groups are introduced into the molecule of Indanthren Yellow GK in positions 4 and 8 the shade becomes violet; this product is manufactured as Indanthren Brilliant Violet BBK.

This entry has not yet been fully updated (first published 1976; most recently modified version published online December 2020).

单词	indanthrene
释义	indanthrenen. /ˈɪndənθriːn/ Forms: Also Indanthren(e. Etymology: < indo- comb. form² + anth- (in anthra- comb. form) + -ene comb. form. (a) (With lower-case initial.) Indanthrone, C₂₈H₁₄N₂O₄ (in quot. 1921 used for the oxygen-free parent compound, C₂₈H₁₈N₂: cf. quot. 1920). (b) (Usually with capital initial.) Any of a large and important class of vat dyes derived from or containing indanthrone or other compounds based on the anthraquinone nucleus.Indanthren(e) has been registered as a proprietary term in Great Britain. ΘΚΠ the world > matter > chemistry > organic chemistry > organic compounds > [noun] > other organic compounds xanthide1823 idrialin1838 barégin1863 violantin1866 biguanide1881 turmerol1890 tetrazole1892 oxazolone1899 indanthrene1901 silicone1906 platinum blue1908 hydroxycitronellal1929 haloform1931 octamethylcyclotetrasiloxane1946 organo-siloxane1946 chlorofluorocarbon1947 permethrin1975 CFC1976 the world > matter > colour > colouring > colouring matter > [noun] > dye > types of dyes pallOE sanders1329 raddlea1350 nutgallc1450 bark1565 logwood1581 sanders-wood1615 catechu1682 cate1698 cachou1708 valonia1722 India wood1742 cutch1759 alizari1769 standard1808 iron buff1836 colorine1838 acid dye1840 garancin1843 French tub1846 suranji1848 morindin1849 water blue1851 union dye1852 indigo-carmine1855 hernant1858 pigment colour1862 rosaniline1862 rose aniline1862 bezetta1863 bottom1863 acid colour1873 paraphenylenediamine1873 indigo-extract1874 tin-pulp1874 phthalein1875 sightening1875 chrome1876 rose bengal1878 azo-colours1879 azine1887 basic dye1892 chromotrope1893 garance1896 ice colour1896 xylochrome1898 cross-dye1901 indanthrene1901 Lithol1903 vat dye1903 thioindigo1906 para red1907 vat colour1912 vat dyestuff1914 indanthrone1920 ionamine1922 Soledon1924 Solochrome1924 Solacet1938 indigoid1939 thioindigoid1943 fluorol1956 Procion1956 the world > matter > colour > named colours > blue or blueness > blue colouring matter > [noun] > dyes and dyestuffs > other dyes stone-blue1675 starch blue1742 Saxon blue1753 fig-blue1786 chemic1792 Turkey blue1815 Paris blue1835 Saxony blue1857 soluble blue1879 methylene blue1882 indoin1884 phenylene blue1884 indamine1888 Nile blue1888 gallamine blue1889 neutral blue1889 chrome-blue1892 toluidine blue1898 indanthrene1901 Saxe blue1905 trypan blue1911 mandarin blue1912 1901 Trade Marks Jrnl. 23 Oct. 1063 Indanthrene. 1901 Jrnl. Soc. Dyers & Colourists 17 (facing p. 302) Indanthrene X is a blue paste insoluble in water. 1901 Jrnl. Soc. Dyers & Colourists 17 (facing p. 302) Indanthrene S is a coppery coloured paste which is soluble in hot water. 1903 Jrnl. Chem. Soc. 84 i. 446 The substance ‘A’, of the German Patent 135407,..can be purified by dissolving it in concentrated sulphuric acid and allowing the solution to gradually absorb water; well-formed, blue needles separate which, in the case of ‘Indanthrene C’, have the composition C₂₈H₁₀O₄N₂Br₂, and, in the case of indanthrene itself, the composition C₂₈H₁₂O₄ N₂. 1920 F. A. Mason tr. G. von Georgievics Text-bk. Dye Chem. (ed. 2) 452 Flavanthrone..is sold as Indanthrene Yellow G (B.A.S.F.), Chloranthrene Yellow (B.D.L.), and Caledon Yellow G (Sol.). 1920 F. A. Mason tr. G. von Georgievics Text-bk. Dye Chem. (ed. 2) 449 Indanthrene (or more correctly Indanthrone, which expresses the quinoid character of the compound, whereas the name generally used would correspond to an oxygen-free compound) is a dianthraquinone-dihydroazine. 1921 E. de B. Barnett Anthracene & Anthraquinone xvi. 342 The first cyclic azine of the anthraquinone series to be prepared was trans. bisang.-anthraquinonedihydro azine. This was placed on the market under the name Indanthrene Blue, and the name ‘indanthrene’ has come into general use in the literature. The word ‘indanthrene’, however, is a registered trade name (B.A.S.F.) and is applied to many vat dyes which are not azines. Indanthrene Blue is an anthraquinone derivative and ketonic in structure, and in order to denote its ketonic nature the name should terminate in -one. In the following pages, therefore, the word ‘indanthrone’ is used to denote the ketonic hydroazine, indanthrene (without a capital) being used for the parent, oxygen free hydroazine (trans. bisang.-dihydroanthrazine). Where ‘Indanthrene’ is used as a registered trade name it is spelt with a capital. 1922 Trade Marks Jrnl. 8 Nov. 2019 Indanthren. 1952 K. Venkataraman Chem. Synthetic Dyes II. xxx. 861 With the amalgamation of the German dyemakers into the IG in 1924, Indanthrene was adopted as the group name for vat dyes with the maximum all-round fastness. 1961 S. R. Cockett & K. A. Hilton Dyeing of Cellulosic Fibres i. 13 In 1901, the first anthraquinone vat dye, Indanthrone (Indanthrene Blue B), was discovered by Bohn... This was followed in the same year, and from the same chemist, by Flavanthrone (Indanthrene Yellow G) and many other variations. 1971 R. L. M. Allen Colour Chem. x. 163 If hydroxyl groups are introduced into the molecule of Indanthren Yellow GK in positions 4 and 8 the shade becomes violet; this product is manufactured as Indanthren Brilliant Violet BBK. This entry has not yet been fully updated (first published 1976; most recently modified version published online December 2020). < n.1901
随便看	to have one's foot on one's native heath to have one's forth to have one's garret unfurnished to have one's guts about one's ears to have one's hand in to have one's hand in the till to have one's hand on another halfpenny to have one's hand on one's halfpenny to have one's hands free to have one's hands full to have one's hat chalked to have one's head in the clouds to have one's head screwed on right to have one's head screwed on the right way to come to good pass to come to grapnel to come to grasp to come to grief to come to gripes to come to grips to come to hand to come to hand blows to come to handgrips to come to handicuffs to come to hands