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Detail of "912-60-7"

  • CAS Number:
  • 912-60-7
  • Name:
  • 1(3H)-Isobenzofuranone,6,7-dimethoxy-3-[(5R)-5,6,7,8-tetrahydro-4-methoxy-6-methyl-1,3-dioxolo[4,5-g]isoquinolin-5-yl]-,hydrochloride (1:1), (3S)-

  • Superlist Name:
  • Noscapine hydrochloride
  • Molecular Structure:
  • Formula:
  • C22H23 N O7 . Cl H
  • Molecular Weight:
  • 449.92
  • Synonyms:
  • 1(3H)-Isobenzofuranone,6,7-dimethoxy-3-(5,6,7,8-tetrahydro-4-methoxy-6-methyl-1,3-dioxolo[4,5-g]isoquinolin-5-yl)-,hydrochloride, [S-(R*,S*)]-; 1(3H)-Isobenzofuranone,6,7-dimethoxy-3-[(5R)-5,6,7,8-tetrahydro-4-methoxy-6-methyl-1,3-dioxolo[4,5-g]isoquinolin-5-yl]-,hydrochloride, (3S)- (9CI); Narcotine, hydrochloride (7CI,8CI);1,3-Dioxolo[4,5-g]isoquinoline, 1(3H)-isobenzofuranone deriv.; Noscapinehydrochloride; Opianine hydrochloride; l-Narcotine hydrochloride
  • Density:
  • 1.332g/cm3
  • Melting Point:
  • 221-223 °C(lit.)
  • Boiling Point:
  • 565.3°Cat760mmHg
  • Flash Point:
  • 295.7°C
  • Hazard Symbols:
  • Risk Codes:
  • 22
  • Safety:
  • Poison by intravenous route. Moderately toxic by ingestion and subcutaneous routes. Mutation data reported. When heated to decomposition it emits very toxic fumes of HCl and NOx. Details

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CAS No.912-60-7 Noscapine hydrochloride

supply high quality 1(3H)-Isobenzofuranone,6,7-dimethoxy-3-[(5R)-5,6,7,8-tetrahydro-4-methoxy-6-methyl-1,3-dioxolo[4,5-g]isoquinolin-5-yl]-,hydrochloride (1:1), (3S)- at good prices. contact us with your email address for details.

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CAS No.912-60-7 Noscapine hydrochloride

Noscapine Hydrochloride

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CAS No.912-60-7 Noscapine hydrochloride

Noscapine

Supplier:shreeji pharma international [ India]

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CAS No.912-60-7 Noscapine hydrochloride

Noscapine hydrochloride

Supplier:Beijing Earlybird Industry Development Co.,Ltd [ China (Mainland)]

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CAS No.912-60-7 Noscapine hydrochloride

Supplier:Alkaloids Corporation [ India]

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CAS No.912-60-7 Noscapine hydrochloride

Supplier:Hubei Hengluyuang Technology Co.,Ltd [ China (Mainland)]

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Reference

Comparative bioavailability and pharmacokinetics of noscapine hydrogen embonate and noscapine hydrochloride
Comparative bioavailability and pharmacokinetics of noscapine hydrogen embonate and noscapine hydrochloride. Haikala, V.; Sothmann, A.; Marvola, M. (Univ. Pharm., Univ. Helsinki, Helsinki SF-00510, Finland). Eur. J. Clin. Pharmacol., 31(3), 367-9 (English) 1986. CODEN: EJCPAS. ISSN: 0031-6970. DOCUMENT TYPE: Journal CA Section: 63 (Pharmaceuticals) Section cross-reference(s): 1 The relative bioavailability and pharmacokinetics of two orally administered aq. suspensions of noscapine hydrogen embonate [106611-48-7] were compared with those of a noscapine HCl [912-60-7] soln in volunteers. Noscapine HCl showed faster absorption and gave a higher peak concn. than the embonate. The av. bioavailability of the embonates was 70% of that of the noscapine soln. No significant difference was obsd. when the embonate was administered with water, polyvidone [9003-39-8] and flavoring agents.
Determination of antitussives, expectorants, and antihistaminic agents in anti-cold preparations by high-speed liquid chromatography
Determination of antitussives, expectorants, and antihistaminic agents in anti-cold preparations by high-speed liquid chromatography. Tatsuzawa, Masayoshi; Hashiba, Shigeko; Ejima, Akira (Natl. Inst. Hyg. Sci., Tokyo, Japan). Eisei Kagaku, 23(5), 282-9 (Japanese) 1977. CODEN: ESKGA2. ISSN: 0013-273X. DOCUMENT TYPE: Journal CA Section: 64 (Pharmaceutical Analysis) Glyceryl guaiacol ether [93-14-1], noscapine [128-62-1], noscapine-HCl [912-60-7], chlorpheniramine maleate [113-92-8], diphenhydramine salicylate [7491-10-3], diphenhydramine-HCl [147-24-0], promethazine methylenedisalicylate [66277-13-2], alimemazine tartrate [4330-99-8], and isothipendyl-HCl [1225-60-1] in anticold prepns. were sepd. successfully by styrene-divinylbenzene copolymer gel or poly(methacrylate) gel as a stationary phase and a mixt. of MeOH and conc. ammonia water as a mobile phase. The sepd. ingredients were detected by spectrophotometry using a UV monitor. Methylephedrine-HCl (I) [942-46-1] was undetected by this method because of its low sensitivity. It had to be sepd. from other ingredients by an ion-exchanger. The sepd. I was oxidized with K ferricyanide, chromatographed, and quantitated by substituting MeOH for the mixt. of MeOH and concd. ammonia water in this procedure.
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