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CAS No 518-82-1 , 1,3,8-trihydroxy-6-methylanthracene-9,10-dione

  • Name: 1,3,8-trihydroxy-6-methylanthracene-9,10-dione
  • Synonyms: Emodol; Rheum emodin; 3-Methyl-1,6,8-trihydroxyanthraquinone;518-82-1; Schuttgelb; Persian Berry Lake; Frangula emodin;1,3,8-trihydroxy-6-methylanthracene-9,10-dione;
  • CAS Registry Number:
  • Melting Point: 253-257 ºC
  • Density: 1.583 g/cm3
  • Water Solubility: <0.1 G/100 ML AT 19 ºC
  • Safety Statements: R36/37/38
  • Hazard Symbols: Xi: Irritant;
  • EINECS: 208-258-8
  • Molecular Weight: 270.2369
  • InchiKey: RHMXXJGYXNZAPX-UHFFFAOYSA-N
  • InChI: InChI=1S/C15H10O5/c1-6-2-8-12(10(17)3-6)15(20)13-9(14(8)19)4-7(16)5-11
    (13)18/h2-5,16-18H,1H3
  • Risk Statements: S26;S37/39
  • Molecular Formula: C15H10O5
  • Molecular Structure:CAS No:518-82-1 1,3,8-trihydroxy-6-methylanthracene-9,10-dione

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References of 1,3,8-trihydroxy-6-methylanthracene-9,10-dione
Title: Emodin
CAS Registry Number: 518-82-1
CAS Name: 1,3,8-Trihydroxy-6-methyl-9,10-anthracenedione
Synonyms: 1,3,8-trihydroxy-6-methylanthraquinone; 4,5,7-trihydroxy-2-methylanthraquinone; frangula emodin; rheum emodin; archin; frangulic acid
Molecular Formula: C15H10O5
Molecular Weight: 270.24
Percent Composition: C 66.67%, H 3.73%, O 29.60%
Literature References: Occurs mostly as the rhamnoside (see Frangulin) in rhubarb root, in alder buckthorn (Rhamnus frangula L.), in Cascara sagrada (Rhamnus purshiana DC., Rhamnaceae), also in Rumex and in other Polygonaceae. Isoln from rhubarb root: Tutin, Clewer, J. Chem. Soc. 99, 946 (1911); Carelli, Giuliano, Farmaco Ed. Prat. 12, 184 (1957); from bark of alder buckthorn: Bridel, Charaux, Bull. Soc. Chim. Biol. 15, 648 (1933). Identity with archin: Chaudhry et al., J. Sci. Ind. Res. 9B, No. 6, 142 (1950), C.A. 44, 9396h (1950). Synthesis from 3,5-dinitrophthalic anhydride and m-cresol: Elder, Widmer, Helv. Chim. Acta 6, 966 (1923); from 2-methylanthraquinone: Ayyangar et al., J. Sci. Ind. Res. 20B, 493 (1961), C.A. 57, 8514b (1962).
Properties: Orange needles from alc or by sublimation at 12 mm. mp 256-257°. Absorption max (ethanol): 222, 252, 265, 289, 437 nm (log e 4.55, 4.26, 4.27, 4.34, 4.10). Practically insol in water; sol in alc, aq alkali hydroxide solns (cherry-red color), Na2CO3 and NH3 solns. Soly at 25° (g/100 ml of satd soln): ether 0.140; chloroform 0.071; carbon tetrachloride 0.010; carbon bisulfide 0.009; benzene 0.041.
Melting point: mp 256-257°
Absorption maximum: Absorption max (ethanol): 222, 252, 265, 289, 437 nm (log e 4.55, 4.26, 4.27, 4.34, 4.10)
 
Derivative Type: 3-Methyl ether
Synonyms: 1,8-Dihydroxy-3-methoxy-6-methylanthraquinone; rheochrysidin
Molecular Formula: C16H12O5
Molecular Weight: 284.26
Percent Composition: C 67.60%, H 4.26%, O 28.14%
Properties: Brick-red, monoclinic needles, mp 207°. Occurs naturally as physcione or parietin.
Melting point: mp 207°
 
Derivative Type: Trimethyl ether
Molecular Formula: C18H16O5
Molecular Weight: 312.32
Percent Composition: C 69.22%, H 5.16%, O 25.61%
Properties: Pale yellow needles, mp 225°.
Melting point: mp 225°
 
NOTE: See also Aloe emodin.
Therap-Cat: Cathartic.
Keywords: Laxative/Cathartic.