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Rhein

  • CAS No.: 478-43-3
  • Purity: 99%
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China cas 478-43-3 manufacturer wholesale Rhein at affordable price

  • Molecular Formula: C15H8O6
  • Molecular Weight: 284.225
  • Appearance/Colour: Yellowish brown solid 
  • Vapor Pressure: 3.85E-15mmHg at 25°C 
  • Melting Point: ≥300 °C(lit.) 
  • Refractive Index: 1.4413 (estimate) 
  • Boiling Point: 597.8 °C at 760 mmHg 
  • PKA: 3.17±0.20(Predicted) 
  • Flash Point: 329.4 °C 
  • PSA: 111.90000 
  • Density: 1.687 g/cm3 
  • LogP: 1.57140 

Rhein(Cas 478-43-3) Usage

Physical and Chemical Properties

The chemical name of Rhein is 1,8-dihydroxy anthraquinone-3-carboxylic acid, with the molecular formula C15H8O6 and the molecular weight of 284.21. It becomes yellow acicular crystal after sublimation, with the melting point 321~322 ℃ and decomposition temperature 330 ℃ and UVλmax (methanol) 229, 258, 435nm. It is soluble in alkali and pyridine, and slightly soluble in alcohol, ether, benzene, chloroform, petroleum ether, and insoluble in water. It can form red sylvine and pink sodium salt, and form a red precipitate with calcium hydroxide and barium hydroxide. Production Method: being acquired from the hydrolysis of Rhein diacetic ester. diethyl acetate. Uses: Current clinical treatment of rheumatic drugs often contain Rhein. Rhein is extracted from the root of the plant Rheum palmatum L. in Polygonaceae family, which is a anthraquinones and has the functions of antibacterial, anti-cancer, cathartic, and diuretic. The contents of rhein, aloe-emodin and rheum emodin in rhubarb are listed in the following table: Table 1. The contents of rhein, aloe-emodin and rheum emodin in rhubarb (n=2%).

Pharmacological effects

There are chemical compounds chrysophanic acid, rhein, aloe-emodin, rheum emodin, aloe emodin, and Sennoside in rhubarb. Both the rhein and rheum emodin have the anti-tumor effect, especially a strong inhibitory effect for melanoma and they have certain inhibition on breast cancer and ehrlich’s ascites carcinoma. When rhein was applied to intratumoral administration in mice with breast cancer, there was a significant damaging in the cancer tissue. The inhibition rate of 5mg/kg rhein and rheum emodin on murine melanoma was 76% and 73%, respectively. Rheum emodin has significant competitive inhibition on tyrosinase, and this inhibition may be one of the mechanisms why rhubarb has the anti-melanoma effect. At the concentration of 10μg/ml, Rheum emodin significantly inhibited the cell division and DNA biosynthesis of human lung cancer A-549 cells. After the subcutaneous injection of crude extracts of rhubarb, an inhibition of mouse sarcoma S37 was found. The inhibition rate of Rhein on ehrlich’s ascites carcinoma and sarcoma S180 in mice was 15% and 21%, respectively. The inhibition rate of hot water extracts of Rhubarb on sarcoma S180 in mice was 48.8%. Rhein has inhibition effect on mouse leukemia P388. Rhein, aloe-emodin and rheum emodin are extracted from rhubarb and these three anthraquinone derivatives could minimize the amount of ascites and the number of cancer cells in different extent in mice with tumors, among which the effect of rhein was most obvious and the effect of aloe-emodin was poorer, with a almost parallel relationship with prolonged survival time. The inhibition of rhein and rheum emodin on biosynthesis of DNA, RNA and protein was stronger, whereas the inhibition of aloe-emodin was weaker.

Air & Water Reactions

Insoluble in water.

Reactivity Profile

Rhein forms a red potassium salt and a pink sodium salt.

Hazard

Low toxicity by ingestion.

Fire Hazard

Flash point data for Rhein are not available; however, Rhein is probably combustible.

Biochem/physiol Actions

Constituent that is enriched in rhubarb with anti-inflammatory, anti-osteoarthritic, and anti-cancer activity. It reduces IL-1β production and secretion, caspase-3 activity, inducible nitric oxide synthase activity, and phosphorylation of c-Jun and c-Jun NH2-terminal kinase (JNK).

Safety Profile

A poison by intravenous route. Low toxicity by ingestion. When heated to decomposition it emits acrid smoke and irritating vapors.

General Description

Yellow needles (from methanol) or yellow-brown powder.

InChI:InChI=1/C15H8O6/c16-9-3-1-2-7-11(9)14(19)12-8(13(7)18)4-6(15(20)21)5-10(12)17/h1-5,16-17H,(H,20,21)/p-1

478-43-3 Relevant articles

Synthesis and pharmacokinetic profile of rhein- boswellic acid conjugate

Suneela, Dhaneshwar,Dipmala, Patil

, p. 7582 - 7587 (2012)

Rhein, an active metabolite of diacerein...

A biocatalytic approach towards the preparation of natural deoxyanthraquinones and their impact on cellular viability

Das, Kiran,De, Arijit,Husain, Syed Masood,Maity, Biswanath,Mondal, Amit,Rajput, Anshul

, p. 3087 - 3090 (2022/02/21)

Herein, a two-step chemoenzymatic proces...

Synthesis of rhein and diacerein: a chemoenzymatic approach using anthrol reductase of Talaromyces islandicus

Rajput, Anshul,Mondal, Amit,Pandey, Satyendra Kumar,Husain, Syed Masood

supporting information, p. 358 - 361 (2022/01/20)

Herein, we report two methods for the sy...

Bis(methoxypropyl) ether-promoted oxidation of aromatic alcohols into aromatic carboxylic acids and aromatic ketones with O2 under metal- and base-free conditions

Liu, Kai-Jian,Jiang, Si,Lu, Ling-Hui,Tang, Ling-Li,Tang, Shan-Shan,Tang, Hai-Shan,Tang, Zilong,He, Wei-Min,Xu, Xinhua

supporting information, p. 3038 - 3043 (2018/07/13)

We describe an eco-friendly, practical a...

Industrial production method suitable for diacerein

-

, (2018/07/30)

The invention discloses an industrial pr...

478-43-3 Process route

sennidin A-8-monoglucoside
82334-26-7,82373-27-1,111144-51-5

sennidin A-8-monoglucoside

1,8-dihydroxy-3-carboxy-anthraquinone
478-43-3

1,8-dihydroxy-3-carboxy-anthraquinone

sennidin B
517-44-2

sennidin B

sennidin A
517-44-2,641-12-3,57762-62-6,67479-20-3,98461-42-8

sennidin A

Conditions
Conditions Yield
With supernatant fluid of rat feces; at 37 ℃; for 2h; Product distribution; anaerobic incubation;
diacetylrhein
13739-02-1

diacetylrhein

1,8-dihydroxy-3-carboxy-anthraquinone
478-43-3

1,8-dihydroxy-3-carboxy-anthraquinone

Conditions
Conditions Yield
With sodium carbonate; In water;
100%
diacetylrhein; With water; sodium carbonate;
With hydrogenchloride; In water; pH=2;
100%
With sodium hydroxide; In water; for 0.5h;
60%
With methanol; potassium hydroxide;
In sodium carbonate;
diacetylrhein; With water; potassium hydroxide; In methanol; at 60 - 65 ℃; for 0.5h;
With hydrogenchloride; In methanol; water; for 0.5h; Reflux;

478-43-3 Upstream products

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    diacetylrhein

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    1,8,9-triacetoxy-3-methyl-anthracene

  • 517-44-2
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    sennidin B

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    517-44-2

    (+)-4,5,4',5'-tetrahydroxy-10,10'-dioxo-9,10,9',10'-tetrahydro-[9,9']bianthryl-2,2'-dicarboxylic acid

478-43-3 Downstream products

  • 13739-02-1
    13739-02-1

    diacetylrhein

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    120-12-7

    anthracene

  • 480-09-1
    480-09-1

    rhein anthrone

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    864652-90-4

    4,5-bis(2-benzyloxyacetyloxy)-9,10-dioxo-9,10-dihydroanthracene-2-carboxylic acid

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