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Detail of "1095-90-5"

  • MSDS Download
  • CAS Number:
  • 1095-90-5
  • Name:
  • 3-Heptanone,6-(dimethylamino)-4,4-diphenyl-, hydrochloride (1:1)

  • Superlist Name:
  • Methadone hydrochloride
  • Molecular Structure:
  • Formula:
  • C21H27NO.HCl
  • Molecular Weight:
  • 345.95
  • Deleted CAS:
  • 125-56-4,70172-45-1,70181-39-4
  • Synonyms:
  • Methadose;Miadone;Moheptan;NSC 19600;Phenadone hydrochloride;Polamidon;Racemicmethadone hydrochloride;dl-6-Dimethylamino-4,4-diphenyl-3-heptanone hydrochloride;dl-Methadone hydrochloride;4,4-Diphenyl-6-dimethylamino-3-heptanone hydrochloride;6-Dimethylamino-4,4-diphenyl-3-heptanone hydrochloride;AN 148;Adanon;Adanonhydrochloride;Algolysin;Amidon;Depridol;Diaminon hydrochloride;Dolophin hydrochloride;Dolophine;Fenadone;Ketalgin;Ketalgin hydrochloride;Mecodin;Mephenon;
  • EINECS:
  • 214-140-7
  • Boiling Point:
  • 423.7 °C at 760 mmHg
  • Flash Point:
  • 126.5 °C
  • Solubility:
  • 120 mg/mL in water
  • Appearance:
  • White solid
  • Hazard Symbols:
  • ToxicT, FlammableF
  • Risk Codes:
  • 25-39/23/24/25-23/24/25-11
  • Safety:
  • 45-36/37 Details
  • Transport Information:
  • UN 2811

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CAS No.1095-90-5 Methadone hydrochloride

Methadone Hydrochloride (CII), USP

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CAS No.1095-90-5 Methadone hydrochloride

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CAS No.1095-90-5 Methadone hydrochloride

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CAS No.1095-90-5 Methadone hydrochloride

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CAS No.1095-90-5 Methadone hydrochloride

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CAS No.1095-90-5 Methadone hydrochloride

METHADONE HYDROCHLORIDE ORAL CONCENTRATE UNFLAVORED OR CHEERY USP is readily available in all forms to our client worldwide with free next day shipping. email back for details and more

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CAS No.1095-90-5 Methadone hydrochloride

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Supplier:Haihang Industry Co.,Ltd. [ China (Mainland)]

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CAS No.1095-90-5 Methadone hydrochloride

Supplier:shanghai sphchem co.,ltd [ China (Mainland)]

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Reference

Methadone hydrochloride: effects of acute administration on disposition and hepatic function in guinea pigs
Methadone hydrochloride: effects of acute administration on disposition and hepatic function in guinea pigs. Pak, R. C. K.; Ecobichon, D. J. (Dep. Pharmacol. Ther., McGill Univ., Montreal, Que., Can.). Can. J. Physiol. Pharmacol., 56(4), 610-16 (English) 1978. CODEN: CJPPA3. ISSN: 0008-4212. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacodynamics) After administration of 10 or 25 mg d,l-methadone-HCl (I) [1095-90-5] to adult female albino guinea pigs, the b-phase plasma half-lives were 13.2 and 13.8 h, resp. Animals treated with 6 consecutive daily doses of I showed peak plasma and hepatic levels by day 2 of the treatment followed by a gradual decline on subsequent days. I did not initially affect either hepatic monooxygenase [9038-14-6] or aniline hydroxylase [9012-80-0] activities. Significant decrease of glucuronyltransferase [37329-64-9] activity was obsd. 24 h after the initial dose. No overt toxicity was obsd. with I administration.
Effects of chronic methadone treatment on maternal body weight and food and water consumption in rats
Effects of chronic methadone treatment on maternal body weight and food and water consumption in rats. White, William J.; McLaughlin, Patricia J.; Zagon, Ian S. (Milton S. Hershey Med. Cent., Pennsylvania State Univ., Hershey, Pa., USA). Pharmacology, 17(4), 227-32 (English) 1978. CODEN: PHMGBN. ISSN: 0031-7012. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacodynamics) Body wt. gain and food and water consumption of female rats receiving daily methadone-HCl [1095-90-5] injections (5 mg/kg) i.p. prior to mating and during gestation and lactation were studied. In contrast to saline-injected controls, methadone-treated females had lower body wts. throughout pregnancy, but gained wt. during lactation; by postnatal day 21, both groups were of comparable body wt. No significant differences in food consumption throughout gestation or lactation were recorded. Total water consumption of methadone-treated rats was higher during the first 2 wk of gestation and lactation, and lower during the 3rd week of lactation when compared to controls. Thus, methadone-treated rats have lower body wts. throughout gestation and lactation, and that these wt. deficits are not caused by insufficient food and water consumption.
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