Anthraquinone
- CAS No.
- 84-65-1
- Chemical Name:
- Anthraquinone
- Synonyms
- AQ;9,10-Anthracenedione;anthracene-9,10-dione;9,10-ANTHRAQUINONE;Anthracenedione;MORKIT;9,10-anthracenequinone;CORBIT;Hoelite;GAUCHO BLE
- CBNumber:
- CB5420557
- Molecular Formula:
- C14H8O2
- Molecular Weight:
- 208.21
- MDL Number:
- MFCD00001188
- MOL File:
- 84-65-1.mol
- MSDS File:
- SDS
| Melting point | 284-286 °C (lit.) |
|---|---|
| Boiling point | 379-381 °C (lit.) |
| Density | 1.438 |
| vapor density | 7.16 (vs air) |
| vapor pressure | 1 mm Hg ( 190 °C) |
| refractive index | 1.5681 (estimate) |
| Flash point | 365 °F |
| storage temp. | no restrictions. |
| solubility | 0.00007g/l |
| form | Powder |
| color | Yellow-green to khaki to tan |
| Water Solubility | <0.1 g/100 mL at 23 ºC |
| Merck | 14,687 |
| BRN | 390030 |
| Stability | Stable. Incompatible with strong oxidizing agents. Combustible. |
| InChIKey | RZVHIXYEVGDQDX-UHFFFAOYSA-N |
| LogP | 3.39-3.4 at 30℃ |
| Indirect Additives used in Food Contact Substances | 9,10-ANTHRAQUINONE |
| CAS DataBase Reference | 84-65-1(CAS DataBase Reference) |
| EWG's Food Scores | 2 |
| NCI Dictionary of Cancer Terms | anthracenedione; anthraquinone |
| FDA UNII | 030MS0JBDO |
| Proposition 65 List | Anthraquinone |
| IARC | 2B (Vol. 101) 2013 |
| NIST Chemistry Reference | 9,10-Anthraquinone(84-65-1) |
| EPA Substance Registry System | Anthraquinone (84-65-1) |
SAFETY
Risk and Safety Statements
| Symbol(GHS) |   GHS07,GHS08 |
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Signal word | Danger | |||||||||
| Hazard statements | H317-H350 | |||||||||
| Precautionary statements | P202-P261-P272-P280-P302+P352-P308+P313 | |||||||||
| Hazard Codes | Xi | |||||||||
| Risk Statements | 43-36/37/38 | |||||||||
| Safety Statements | 36/37-37/39-26-24 | |||||||||
| RIDADR | 3077 | |||||||||
| WGK Germany | 1 | |||||||||
| RTECS | CB4725000 | |||||||||
| Autoignition Temperature | 650 °C | |||||||||
| TSCA | Yes | |||||||||
| HS Code | 2914 61 00 | |||||||||
| HazardClass | 9 | |||||||||
| PackingGroup | III | |||||||||
| Toxicity | LD50 orally in Rabbit: > 5000 mg/kg | |||||||||
| NFPA 704 |
|
Anthraquinone price More Price(31)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Sigma-Aldrich | 8.00465 | Anthraquinone for synthesis | 84-65-1 | 100g | $38.7 | 2024-03-01 | Buy |
| Sigma-Aldrich | 8.00465 | Anthraquinone for synthesis | 84-65-1 | 500g | $85.4 | 2024-03-01 | Buy |
| Sigma-Aldrich | 67372 | Melting point standard 283-286°C analytical standard | 84-65-1 | 250mg | $55.5 | 2024-03-01 | Buy |
| Sigma-Aldrich | 67372 | Melting point standard 283-286°C analytical standard | 84-65-1 | 1g | $194 | 2024-03-01 | Buy |
| TCI Chemical | A0502 | Anthraquinone >98.0%(GC) | 84-65-1 | 25g | $29 | 2024-03-01 | Buy |
Anthraquinone Chemical Properties,Uses,Production
Description
Anthraquinone is a combustible, light yellowto green crystalline solid. Molecular weight= 208.23;Boiling point= 380℃; Melting/Freezing point= 286℃(sublimes); Flash point= 185℃ (cc). NFPA 704 M HazardIdentification (based on NFPA-704 M Rating System):Health 0, Flammability 1, Reactivity 0. Very slightly solublein water; solubility=,13 mg/L at 22℃.
Chemical Properties
Anthraquinone is a combustible, light yellow to green crystalline solid. Soluble in ethanol, ether and acetone, insoluble in water. It may be prepared by reacting benzene with phthalic anhydride. The compoundis the basis of a range ofdyestuffs.
Occurrence
Anthraquinones naturally occur in some plants (eg. aloe, senna, rhubarb, and Cascara buckthorn), fungi, lichens, and insects, where they serve as a basic skeleton for their pigments. Natural anthraquinone derivatives tend to have laxative effects.
Uses
Anthraquinone is used in paper industry as a catalyst to increase the pulp production yield and to improves the fiber strength through reduction reaction of cellulose to carboxylic acid. It is also used as a precursor for dye formation.
Definition
ChEBI: Anthraquinone is an anthraquinone that is anthracene in which positions 9 and 10 have been oxidised to carbonyls. It is a colorless crystalline quinone used in producing dyestuffs such as alizarin.
Preparation
Anthraquinone is obtained by oxidation of anthracene using sodium dichromate plus sulfuric acid, and is purified by dissolving in concentrated sulfuric acid at 130 °C and pouring into boiling water, whereupon anthraquinone separates as pure solid, and is recovered by filtration. Further purification may be accomplished by sublimation or crystallization from nitrobenzene, aniline or tetrachloroethane.
Synthesis Reference(s)
Journal of the American Chemical Society, 102, p. 1457, 1980 DOI: 10.1021/ja00524a059
The Journal of Organic Chemistry, 29, p. 987, 1964 DOI: 10.1021/jo01027a538
Tetrahedron Letters, 24, p. 5499, 1983 DOI: 10.1016/S0040-4039(00)94122-4
General Description
Anthraquinone is a polycyclic aromatic hydrocarbon derived from anthracene or phthalic anhydride. Anthraquinone is used in the manufacture of dyes, in the textile and pulp industries, and as a bird repellant.
Air & Water Reactions
Insoluble in water.
Reactivity Profile
Anthraquinone is incompatible with strong oxidizing agents.
Hazard
Possible carcinogen.
Fire Hazard
Anthraquinone is combustible.
Flammability and Explosibility
Non flammable
Agricultural Uses
Repellent, Seed treatment: Used as a seed dressing or protectant. Banned in EU.
Trade name
(p)ANTHRAPEL®; FLIGHT CONTROL- PLUS®; HOELITE®; MORKIT®; REPELL®
Pharmacology
Anthraquinone is a secondary repellent and affects birds by causing post-ingestional distress (40). Sometimes, ingestion of anthraquinone-treated food produces vomiting, but often vomiting does not occur and the bird just sits quietly until the discomfort passes. Unlike methiocarb, anthraquinone doe not affect the bird’s nervous system and does not immobilize affected birds. Presumably, the emetic response is produced through irritation of the gut lining, but the actual mechanism is unclear. It is clear, however, that anthraquinone is not a taste repellent or contact irritant. Birds do not hesitate to eat treated food, and they exhibit no sign that treated food is unpalatable to them. The post-ingestional discomfort that results from eating anthraquinone-treated food produces a conditioned aversion to that food type. Birds need to experience the adverse consequences before learning to avoid the protected food. Thus, it is not reasonable to expect losses to cease immediately upon application of the repellent. There will be some level of loss in the crop as the depredating birds acquire the learned avoidance response.
Safety Profile
Moderately toxic by intraperitoneal route. A mild allergen. Mutation data reported. Combustible when exposed to heat or flame. To fight fire, use water, foam, CO2, water spray or mist, dry chemical. When heated to decomposition it emits acrid smoke and irritating fumes.
Toxicology
Based on present knowledge, anthraquinone, unlike
the “emodins” (hydroxyanthraquinone glycosides)
from anthraquinone drugs , is biologically
completely “inert,” i.e., inactive, presumably
as a consequence of its insolubility in
water and lipids.
There is no toxicologic information about
anthraquinone. Even in the Toxic Substances List
no LD50 is found for anthraquinone. In contrast
to benzoquinone, which causes severe local
irritation and is included in the list of occupational
hazards because of its damaging effect on
the cornea, a fine dust of anthraquinone to which
emulgators were added had no greater effect on
the eyes of rabbits than a talcum suspension, as
was shown in a BASF study.
An MAK value of 10 mg/m3 was recommended
; therefore, anthraquinone dust is
considered the same as inert dust.
Synthesis
Anthraquinone is produced from anthracene,
where this is available from coal tar, either by oxidation
with chromic acid in 48 % sulfuric acid
or by oxidation with air in the vapor phase. The
oxidation with chromic acid is competitive, provided
that the chromium(III) sulfate lye formed
can be processed to tanning agents. Anthracene
with purity of '94 % is required for both oxidation
processes; crude anthracene from coal tar
must be purified by recrystallization.
About 85 % of world production is based
on the oxidation of anthracene. Since the mid-
1970s, anthracene production has fallen continuously,
creating a supply shortage. Therefore, the
complex naphthalene process is gaining in importance.
There is an adequate supply of naphthalene
in coal tar. If necessary, additional naphthalene
can be isolated from the residual oils of
gasoline reforming, a process common in the
United States.
Potential Exposure
Anthraquinone is an important starting material for vat dye manufacture. Also used in making organics; and used as a bird repellent in seeds.
First aid
If this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions,including resuscitation mask) if breathing has stopped andCPR if heart action has stopped. Transfer promptly to amedical facility. When this chemical has been swallowed,get medical attention. Give large quantities of water andinduce vomiting. Do not make an unconscious person vomit.
storage
Color Code—Blue: Health Hazard/Poison: Store ina secure poison location. Prior to working with this chemicalyou should be trained on its proper handling and storage.Store in tightly closed containers in a cool, well-ventilatedarea away from oxidizers. Sources of ignition, such as smoking and open flames, are prohibited where this chemical isused, handled, or stored in a manner that could create apotential fire or explosion hazard.
Shipping
UN3143 Dyes, solid, toxic, n.o.s. or Dye intermediates, solid, toxic, n.o.s., Hazard Class: 6.1; Labels: 6.1-Poisonous materials, Technical Name Required.
Purification Methods
Crystallise anthraquinone from CHCl3 (38mL/g), *benzene, or boiling acetic acid, wash it with a little EtOH and dry it under vacuum over P2O5. [Beilstein 7 IV 2556.]
Toxicity evaluation
Anthraquinone is a stable compound that is virtually insoluble in water. It is not phytotoxic and does not inhibit germination of rice seeds or growth of sprouts. It has very low toxicity to birds and mammals, and it appears to be innocuous to insects as well. There is no known hazard to nontarget species from repellent applications of Flight Control.
Incompatibilities
Incompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides
Waste Disposal
Dissolve or mix the material with a combustible solvent and burn in a chemical incinerator equipped with an afterburner and scrubber. All federal, state, and local environmental regulations must be observed.
Anthraquinone Preparation Products And Raw materials
Raw materials
1of3
Preparation Products
1of5
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| Hebei Weibang Biotechnology Co., Ltd | +8615531157085 | abby@weibangbio.com | China | 8812 | 58 |
| Hebei Saisier Technology Co., LTD | +86-18400010335 +86-18034520335 | admin@hbsaisier.cn | China | 1015 | 58 |
| BINBO BIOLOGICAL CO.,LTD | +8618629063126 | info@binbobiological.com | China | 377 | 58 |
| Hebei Zhuanglai Chemical Trading Co.,Ltd | +8613343047651 | admin@zlchemi.com | China | 3002 | 58 |
| Hebei Longbang Technology Co., LTD | +86-18633929156 +86-18633929156 | admin@hblongbang.com | China | 941 | 58 |
| Hebei Shengyang Water Conservancy Engineering Co., Ltd. | +8615373025980 | clara@hbshengyang.com | China | 874 | 58 |
| Hebei Andu Technology Com.,Ltd | +86-86-17798073498 +8617798073498 | admin@hbandu.com | China | 299 | 58 |
| HebeiShuoshengImportandExportco.,Ltd | +86-18532138899 +86-18532138899 | L18532138899@163.com | China | 939 | 58 |
| Capot Chemical Co.,Ltd. | +86-（0）57185586718 +86-13336195806 | sales@capot.com | China | 29791 | 60 |
| Henan Tianfu Chemical Co.,Ltd. | +86-0371-55170693 +86-19937530512 | info@tianfuchem.com | China | 21634 | 55 |
View Lastest Price from Anthraquinone manufacturers
| Image | Update time | Product | Price | Min. Order | Purity | Supply Ability | Manufacturer | |
|---|---|---|---|---|---|---|---|---|
 |
2024-11-24 | Anthraquinone
84-65-1
|
US $3.50 / kg | 1kg | 0.99 | 3000tons/month | Hebei Andu Technology Com.,Ltd | |
 |
2024-11-22 | Anthraquinone
84-65-1
|
US $60.00 / kg | 1kg | 99 | 5000 | Hebei Zhuanglai Chemical Trading Co.,Ltd | |
 |
2024-11-22 | Anthraquinone
84-65-1
|
US $0.00 / KG | 1KG | 98%min | 30tons/month | WUHAN FORTUNA CHEMICAL CO., LTD |
-
- Anthraquinone
84-65-1
- US $3.50 / kg
- 0.99
- Hebei Andu Technology Com.,Ltd
-
- Anthraquinone
84-65-1
- US $60.00 / kg
- 99
- Hebei Zhuanglai Chemical Trading Co.,Ltd
-
- Anthraquinone
84-65-1
- US $0.00 / KG
- 98%min
- WUHAN FORTUNA CHEMICAL CO., LTD