Home > Name List By d > D-ribo-Hexitol,2,5-anhydro-1,4,6-trideoxy-6-(trimethylammonio)-

CAS No 300-54-9 , D-ribo-Hexitol,2,5-anhydro-1,4,6-trideoxy-6-(trimethylammonio)-

  • Name: D-ribo-Hexitol,2,5-anhydro-1,4,6-trideoxy-6-(trimethylammonio)-
  • Synonyms: [2S-(2a,4b,5a)]-(Tetrahydro-4-hydroxy-5-methylfurfuryl)trimethylammonium;(+)-(2S,4R,5S)-Muscarine; L-(+)-Muscarine;2-Furanmethanaminium,tetrahydro-4-hydroxy-N,N,N,5-tetramethyl-, [2S-(2a,4b,5a)]-; Muscarine (alkaloid) (8CI);D-ribo-Hexitol,2,5-anhydro-1,4,6-trideoxy-6-(trimethylammonio)-; Muscarine; (+)-Muscarine;
  • CAS Registry Number:
  • Melting Point: 174.261
  • Flash Point: °C
  • Boiling Point: °Cat760mmHg
  • Density: g/cm3
  • Safety Statements: Human poison by an unspecified route. Experimental poison by ingestion, intravenous, intraperitoneal, and subcutaneous routes. When heated to decomposition it emits toxic fumes of NOx and NH3.
  • Hazard Symbols: Xn: Harmful;
  • Flash Point: °C
  • EINECS: 206-094-1
  • Molecular Weight: 174.2606
  • InchiKey: UQOFGTXDASPNLL-XHNCKOQMSA-N
  • InChI: InChI=1S/C9H20NO2/c1-7-9(11)5-8(12-7)6-10(2,3)4/h7-9,11H,5-6H2,1-4H3/q+1/t7-,8-,9+/m0/s1
  • Risk Statements: 22-36
  • Molecular Formula: C9H20NO2+
  • Molecular Structure:CAS No:300-54-9 D-ribo-Hexitol,2,5-anhydro-1,4,6-trideoxy-6-(trimethylammonio)-

Related products

Search by region :

Select to

300-54-9 Muscarine

  • IUPAC NAME-2,5-Anhydro-1,4,6-trideoxy-6-(trimethylammonio)-D-ribo-hexitol MOLECULAR FORMULA-C9H20NO2+ MOLAR MASS-174.26 g/mol Muscarine, L-(+)-muscarine, or muscarin is a natural product found in certain mushrooms, particularly in Inocybe and Clitocy...
  • India Swapnroop Drugs & Pharmaceuticals [Manufacturer, Trading Company]
  • Tel: 91-240-6641875
  • Fax: 91-240-6641875
  • Address: Harsool Aurangabad,MaharashtraIndia
Contact Supplier

300-54-9 (+/-)-MUSCARINE CHLORIDE

  • China Rongkang industry Co.,Ltd [Manufacturer]
  • Tel: +86-571-8801 0713
  • Fax: +86-571-8801 0679
  • Address: Rongkang Industry Co.,Ltd
    2-3-1502 XIANGXIELI GARDEN
    NO.4 STREET XIASHA
    HANGZHOU, CHINA P.C:310018 null,nullChina
Contact Supplier

300-54-9 (+ -)-MUSCARINE CHLORIDE

  • United States International Laboratory (IL) [Manufacturer]
  • Tel: 650-278-9963
  • Fax: 650-589-2786
  • Address: 1067 SNEATH LN
    SAN BRUNO
    CA 94066, USA null,nullUnited States
Contact Supplier

300-54-9 (+ -)-Muscarine chloride

  • (+ -)-Muscarine chloride
  • Germany CHEMOS GmbH [Manufacturer]
  • Tel: 0049 9402/9336 0
  • Fax: 0049 9402/9336 13
  • Address: CHEMOS GmbH
    Werner-von-Siemensstr. 3
    93128 Regenstauf
    Germany null,nullGermany
Contact Supplier

300-54-9 (+ -)-MUSCARINE CHLORIDE

  • (+ -)-MUSCARINE CHLORIDE
  • Hong kong Advanced Technology & Industrial Co., Ltd. [Manufacturer]
  • Tel: (852) 2390 2293/ (852) 2394 5546
  • Fax: (852) 2789 8314
  • Address: Unit B, 1/F., Cheong Shing Bldg.,
    17 Walnut St., Tai Kok Tsui, Kln,
    Hong Kong null,nullHong kong
Contact Supplier

Select to

1/1
References of D-ribo-Hexitol,2,5-anhydro-1,4,6-trideoxy-6-(trimethylammonio)-
Title: Muscarine
CAS Registry Number: 300-54-9
CAS Name: [2S-(2a,4b,5a)]-Tetrahydro-4-hydroxy-N,N,N,5-tetramethyl-2-furanmethanaminium
Molecular Formula: [C9H20NO2]+
Literature References: Alkaloid from the red variety of Amanita muscaria (L.) Pers., Agaricaceae, the fly fungus, a poisonous mushroom. Also found in some other fungi: Inocybe patouillardi; I. fastigiata, I. umbrina; I. rimosa. Isoln procedure for the naturally occurring L-(+)-form: Kuehl et al., J. Am. Chem. Soc. 77, 6663 (1955); Eugster, Helv. Chim. Acta 39, 1002 (1956). Structure and synthesis of racemate: K?gl et al., Rec. Trav. Chim. 76, 109 (1957); K?gl et al., Experientia 13, 137, 138 (1957); Cox et al., Helv. Chim. Acta 41, 229 (1958). Alternate syntheses: GB 828395 (1960 to Hoffmann-La Roche); Matsumoto et al., Tetrahedron 25, 5889 (1969); W. C. Still, J. A. Schneider, J. Org. Chem. 45, 3375 (1980). Synthesis of muscarine: Whiting et al., Can. J. Chem. 50, 3322 (1972); A. M. Mubarak, D. M. Brown, Tetrahedron Lett. 21, 2453 (1980); eidem, J. Chem. Soc. Perkin Trans. 1 1982, 809; S. Pochet, T. Huynhdinh, J. Org. Chem. 47, 193 (1982). Chemistry and pharmacology: Waser, Pharmacol. Rev. 13, 465-515 (1961). Toxicity study: P. J. Fraser, Br. J. Pharmacol. 12, 47 (1957). Reviews: C. H. Eugster, Adv. Org. Chem. 2, 427-455 (1960); S. Wilkinson, Q. Rev. Chem. Soc. 15, 153-171 (1961). Configurational relationship in the muscarine series: Bollinger, Eugster, Helv. Chim. Acta 54, 2704 (1971).
 
Derivative Type: Chloride
Molecular Formula: C9H20ClNO2
Molecular Weight: 209.71
Percent Composition: C 51.55%, H 9.61%, Cl 16.91%, N 6.68%, O 15.26%
Properties: Stout prisms from ethanol + acetone, mp 180-181°. Extremely hygroscopic. [a]D25 +8.1° (c = 3.5 in ethanol). Very sol in water, ethanol. Slightly sol in chloroform, ether, acetone. Aq solns are stable. LD50 i.v. in mice: 0.23 mg/kg (Fraser).
Melting point: mp 180-181°
Optical Rotation: [a]D25 +8.1° (c = 3.5 in ethanol)
Toxicity data: LD50 i.v. in mice: 0.23 mg/kg (Fraser)
 
CAUTION: Potential symptoms of toxicity following ingestion are profuse sweating, increased salivation, visual disturbances, nausea, vomiting, abdominal colic, diarrhea, headache, and bronchospasm. Very high doses may produce lacrimation, incontinence, bradycardia, hypotension and shock. See Clinical Toxicology of Commercial Products, R. E. Gosselin et al., Eds. (Williams & Wilkins, Baltimore, 5th ed., 1984) Section II, p 247.
Therap-Cat: Cholinergic.
Keywords: Cholinergic.