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Indigo

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Name

Indigo

EINECS 207-586-9
CAS No. 482-89-3 Density 1.417 g/cm3
PSA 58.20000 LogP 3.09080
Solubility Water: <0.1 g/100 mL Melting Point >300 °C(lit.)
Formula C16H10N2O2 Boiling Point 400.4 °C at 760 mmHg
Molecular Weight 262.268 Flash Point 158.2 °C
Transport Information UN 3264 8/PG 3 Appearance dark violet powder
Safety 26-36 Risk Codes 36/38-36/37/38
Molecular Structure Molecular Structure of 482-89-3 (Indigo) Hazard Symbols IrritantXi
Synonyms

Indigo PureBASF (6CI);[D2,2'-Biindoline]-3,3'-dione(8CI);Blue No. 201;C Blue 22;C.I. Pigment Blue 66;C.I. Vat Blue 1;Cystoceva;Diindogen;Indigo Blue;Indigo Ciba;IndigoCiba SL;Indigo J;Indigo N;Indigo NAC;Indigo Powder W;Indigo Pure BASF Powder K;Indigo Synthetic;Indigo VS;Indigotin;Indigotin (natural);Japan Blue 201;Lithosol Deep BlueB;Mitsui Indigo Paste;MonoliteFast Navy Blue BV;Natural Blue 1;Natural blue indigotin;Pigment Blue 66;Pigment Indigo;Pigment Indigo V;Reduced Dark Blue VB;Synthetic indigo;Vat Blue 1;Vulcafor BlueA;Vulcanosine Dark Blue L;[D2,2'(3H,3'H)-Biindole]-3,3'-dione;D2,2'-Bipseudoindoxyl;

Article Data 244

Indigo Synthetic route

59-48-3

2-oxoindole

612-54-4

2-chloro-3H-indol-3-one

482-89-3

1H,1H'-2,2'-Biindolylidene-3,3'-dione

Conditions
ConditionsYield
In toluene for 1h; Heating;96%
91-56-5

indole-2,3-dione

482-89-3

1H,1H'-2,2'-Biindolylidene-3,3'-dione

Conditions
ConditionsYield
With tetraphosphorus decasulfide In pyridine at 85℃; for 0.0833333h;90%
Multi-step reaction with 2 steps
1: PCl5 / benzene / 4 h / Heating
2: 70 percent / thiophenol / benzene / 4 h / Heating; further thiophenols used: 1) p-CH3C6H4SH, 2) p-ClC6H4SH, 3) m-CH3C6H4SH, 4) o-CH3C6H4SH
View Scheme
Multi-step reaction with 2 steps
1: benzene; phosphorus pentachloride
2: zinc dust; glacial acetic acid
View Scheme
16800-68-3

1-acetyl-2,3-dihydro-1H-indol-3-one

16800-67-2

N,O-diacetylindoxyl

A

110912-08-8

1,2-diacetyl-3-indolinone

B

482-89-3

1H,1H'-2,2'-Biindolylidene-3,3'-dione

Conditions
ConditionsYield
With sulfuric acid In acetic anhydride at 20℃; for 20h;A 88.8%
B n/a
110912-09-9

1-acetyl-2-propionyl-3-indolinone

A

110912-10-2

1-(3-Hydroxy-1H-indol-2-yl)-propan-1-one

B

482-89-3

1H,1H'-2,2'-Biindolylidene-3,3'-dione

Conditions
ConditionsYield
With sodium hydroxide at 20℃; for 2h;A 86.4%
B n/a
110912-08-8

1,2-diacetyl-3-indolinone

A

22079-15-8

1-(3-Hydroxy-1H-indol-2-yl)ethanon

B

482-89-3

1H,1H'-2,2'-Biindolylidene-3,3'-dione

Conditions
ConditionsYield
With sodium hydroxide at 20℃; for 2h;A 85.7%
B n/a
16800-67-2

N,O-diacetylindoxyl

123-62-6

propionic acid anhydride

A

110912-09-9

1-acetyl-2-propionyl-3-indolinone

B

482-89-3

1H,1H'-2,2'-Biindolylidene-3,3'-dione

Conditions
ConditionsYield
With sulfuric acid In acetic anhydrideA 72%
B n/a
612-54-4

2-chloro-3H-indol-3-one

482-89-3

1H,1H'-2,2'-Biindolylidene-3,3'-dione

Conditions
ConditionsYield
With thiophenol In benzene for 4h; Heating; further thiophenols used: 1) p-CH3C6H4SH, 2) p-ClC6H4SH, 3) m-CH3C6H4SH, 4) o-CH3C6H4SH;70%
With hydrogen iodide; acetic acid
With acetic acid; zinc
With ammonium sulfide
With phosphorous
110912-11-3

1-acetyl-2-benzoyl-3-indolinone

A

22078-82-6

2-benzoyl-3-hydroxyindole

B

482-89-3

1H,1H'-2,2'-Biindolylidene-3,3'-dione

Conditions
ConditionsYield
With sodium hydroxide In methanol at 20℃; for 20h;A 67.8%
B n/a
144646-98-0

1-(phenylsulfonyl)-2-trimethylsilylindol-3-yl trifluoromethanesulfonate

482-89-3

1H,1H'-2,2'-Biindolylidene-3,3'-dione

Conditions
ConditionsYield
With tetrabutyl ammonium fluoride In tetrahydrofuran51%
78551-19-6

2,3-dioxo-2,3-dihydro-1H-indole-5-sulfonate

1H-indol-3-ol anion

A

482-89-3

1H,1H'-2,2'-Biindolylidene-3,3'-dione

B

indirubin-5'-sulfonate

Conditions
ConditionsYield
With N,N'-bis(6A-deoxy-β-cyclodextrin-6A-yl)NHCOCONH In water at 20℃; pH=10.0; Product distribution; Further Variations:; Reagents;A 1.8%
B 36%

Indigo Consensus Reports

Reported in EPA TSCA Inventory.

Indigo Specification

The Indigo with the cas number 482-89-3, is also called (2E)-2-(3-oxo-1H-indol-2-ylidene)-1H-indol-3-one named by IUPAC. And it's systemic name are(1)(delta(sup 2,2')-Biindoline)-3,3'-dione; (2)(delta2,2'-Biindoline)-3,3'-dione (8CI) ; (3)2-(1,3-Dihydro-3-oxo-2H-indazol-2-ylidene)-1,2-dihydro-3H-indol-3-one ; (4)2-(1,3-Dihydro-3-oxo-2H-indol-2-ylidene)-1,2-dihydro-3H-indol-3-one ; (5)3H-Indol-3-one, 2-(1,3-dihydro-3-oxo-2H-indol-2-ylidene)-1,2-dihydro-. It belongs to rganics product categories. Besides, it seems like dark blue powder with coppery luster. Indigo occurs in isomeric forms (cis and trans). It is Stable but incompatible with strong oxidizing agents. Water solubility is lower than other edible pigment around 25 ° c. 0.05% solution appears blue. It is soluble in glycerin, propylene glycol, slightly soluble in ethanol, insoluble in grease. It shows darkblue when encounter sulfuric acid, and appear to be blue when diluted. with sodium hydroxide in solution, it turns green and yellow green. And it is sensitive to heat and light. Indigo  is used as a dye for cotton yarn, which is mainly for the production of denim cloth for blue jeans. Small amounts are used for dying wool and silk.

Physical properties about this chemical are: (1)ACD/LogP: 3.72 ; (2)# of Rule of 5 Violations: 0 ; (3)ACD/LogD (pH 5.5): 3.72 ; (4)ACD/LogD (pH 7.4): 3.72 ; (5)ACD/BCF (pH 5.5): 395.55 ; (6)ACD/BCF (pH 7.4): 395.55 ; (7)ACD/KOC (pH 5.5): 2515.82 ; (8)ACD/KOC (pH 7.4): 2515.82 ; (9)#H bond acceptors: 4 ; (10)#H bond donors: 2 ; (11)#Freely Rotating Bonds: 0 ; (12)Polar Surface Area: 40.62Å2 ; (13)Index of Refraction: 1.709 ; (14)Molar Refractivity: 72.22 cm3 ; (15)Molar Volume: 185 cm3 ; (16)Polarizability: 28.63 ×10-24cm3 ; (17)Surface Tension: 63.4 dyne/cm ; (18)Density: 1.417 g/cm3 ; (19)Flash Point: 158.2 °C ; (20)Enthalpy of Vaporization: 65.13 kJ/mol ; (21)Boiling Point: 400.4 °C at 760 mmHg ; (22)Vapour Pressure: 1.27E-06 mmHg at 25°C

Prepration of Indigo: Indigo powder sulfonation by sulfuric acid, diluted by water, neutralization with sodium carbonate, refined by salting-out. Indigo powder (100%) 210kg can be produced at the cost of every tons product. It is an synthesis edible pigment and applied to food, medicine and cosmetics.

1. N-phenylglycine is treated with a molten mixture of sodium hydroxide, potassium hydroxide, and sodamide. This highly sensitive melt produces indoxyl, which is subsequently oxidised in air to form indigo.

2. An alternative and also viable route to indigo involves heating N-(2-carboxyphenyl)glycine to 200 °C in an inert atmosphere with sodium hydroxide. Indoxyl-2-carboxylic acid is generated. This material readily decarboxylates to give indoxyl, which oxidises in air to form indigo.


When you are using this chemical, please be cautious about it as the following: It is quite irritating to eyes, respiratory system and skin. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. Before you are using it, please wear suitable protective clothing. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. 

You can still convert the following datas into molecular structure :
(1).SMILES: O=C/4c1ccccc1NC\4=C3\C(=O)c2ccccc2N3
(2).InChI:InChI=1/C16H10N2O2/c19-15-9-5-1-3-7-11(9)17-13(15)14-16(20)10-6-2-4-8-12(10)18-14/h1-8,17-18H/b14-13+

Toxic information of Indigo can be showed as follows:

Organism Test Type Route Reported Dose (Normalized Dose) Effect Source
mouse LD50 intraperitoneal 2200mg/kg (2200mg/kg)   "Zhongliu Yanjiu" Cancer Review, Yu, R., et al., eds., Shanghai Science/Technology Publisher,Peop. Rep. China, 1994Vol. -, Pg. 173, 1994.
mouse LD50 oral > 32gm/kg (32000mg/kg)   "Zhongliu Yanjiu" Cancer Review, Yu, R., et al., eds., Shanghai Science/Technology Publisher,Peop. Rep. China, 1994Vol. -, Pg. 173, 1994

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