LOFEPRAMINE HYDROCHLORIDE

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Names

[ CAS No. ]:
26786-32-3

[ Name ]:
LOFEPRAMINE HYDROCHLORIDE

[Synonym ]:
N-(4-Chlorobenzoylmethyl)-3-(10,11-dihydro-5h-dibenz[b,f]azepin-5-yl)-n-methylpropylamine hydrochloride
1-(4-chlorophenyl)-2-[3-(5,6-dihydrobenzo[b][1]benzazepin-11-yl)propyl-methylamino]ethanone,hydrochloride
Lofepramine hydrochloride

Chemical & Physical Properties

[ Boiling Point ]:
575ºC at 760 mmHg

[ Molecular Formula ]:
C26H28Cl2N2O

[ Molecular Weight ]:
455.42

[ Flash Point ]:
301.6ºC

[ Exact Mass ]:
454.15800

[ PSA ]:
23.55000

[ LogP ]:
6.64850

[ Vapour Pressure ]:
3.17E-13mmHg at 25°C

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
AM6485000
CHEMICAL NAME :
Acetophenone, 4'-chloro-2-((3-(10,11-dihydro-5H-dibenz(b,f)azepin-5 -yl)propyl)methylamin o)-, hydrochloride
CAS REGISTRY NUMBER :
26786-32-3
LAST UPDATED :
199707
DATA ITEMS CITED :
13
MOLECULAR FORMULA :
C26-H27-Cl-N2-O.Cl-H
MOLECULAR WEIGHT :
455.46
WISWESSER LINE NOTATION :
T676 BN IH JHJ B3N1&1VR DG &GH

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
>5 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
>1 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
>1 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>5 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
920 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Subcutaneous
SPECIES OBSERVED :
Rodent - mouse
DOSE/DURATION :
>1 gm/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
2800 mg/kg/4W-I
TOXIC EFFECTS :
Brain and Coverings - changes in brain weight Nutritional and Gross Metabolic - weight loss or decreased weight gain Related to Chronic Data - death
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
18200 mg/kg/26W-I
TOXIC EFFECTS :
Blood - changes in erythrocyte (RBC) count Nutritional and Gross Metabolic - weight loss or decreased weight gain Nutritional and Gross Metabolic - changes in potassium
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
DOSE :
180 mg/kg
SEX/DURATION :
female 17-22 day(s) after conception
TOXIC EFFECTS :
Reproductive - Effects on Newborn - stillbirth
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
DOSE :
630 mg/kg
SEX/DURATION :
female 14 day(s) pre-mating female 1-7 day(s) after conception
TOXIC EFFECTS :
Reproductive - Specific Developmental Abnormalities - musculoskeletal system
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
DOSE :
150 mg/kg
SEX/DURATION :
female 9-14 day(s) after conception
TOXIC EFFECTS :
Reproductive - Effects on Embryo or Fetus - fetotoxicity (except death, e.g., stunted fetus)
TYPE OF TEST :
TDLo - Lowest published toxic dose
ROUTE OF EXPOSURE :
Oral
DOSE :
1200 mg/kg
SEX/DURATION :
female 7-12 day(s) after conception
TOXIC EFFECTS :
Reproductive - Specific Developmental Abnormalities - musculoskeletal system

MUTATION DATA

TEST SYSTEM :
Insect - Drosophila melanogaster
DOSE/DURATION :
100 mmol/L
REFERENCE :
MUREAV Mutation Research. (Elsevier Science Pub. B.V., POB 211, 1000 AE Amsterdam, Netherlands) V.1- 1964- Volume(issue)/page/year: 286,155,1993

Related Compounds

  • Tyrocidine, hydrochloride
  • Triprolidine hydrochloride
  • Minoxidil hydrochloride
  • Elacridar hydrochloride
  • dodecylamine hydrochloride
  • Azetidine, hydrochloride, homopolymer (9CI)
  • (1S,3aR,3bR,5S,5aR,7S,9aR,9bR,11R,11aR)a1a[(2S)a 2,6adimethoxya6amethylheptana2ayl]a3a,3b,6,6,9aa pentamethylahexadecahydroa1Ha cyclopenta[a]phenanthrenea5,7,11atriol
  • (3beta,6alpha,12beta,20R)-20,24-Epoxydammarane-3,6,12,25-tetrol
  • (1S,3aR,3bR,5aR,7S,9aR,9bR,11R,11aR)a7a(acetyloxy)a1a [(2S)a2,6adihydroxya6amethylheptana2ayl]a 3a,3b,6,6,9aapentamethylahexadecahydroa1Ha cyclopenta[a]phenanthrena11ayl acetat
  • Phosphorothioic acid O-[2-Chloro-1-(1-methylethyl)-1H-imidazol-4-yl] O,O-diethyl ester
  • 2,2-Difluoro-1-(2-methyl-1,3-thiazol-5-yl)ethan-1-amine
  • (1R,3aR,3bS,9bR,11aR)-1-Hydroxy-11a-methyl-1,2,3,3a,3b,4,5,6,8,9,9b,10,11,11a-tetradecahydro-7H-cyclopenta[a]phenanthren-7-one
  • 2-Chloro-6-[(4,6-dimethoxy-2-pyrimidinyl)thio]benzoic acid octyl ester
  • 2-Amino-N-[3-cyano-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazol-5-yl]acetamide
  • 2-(4-Chloro-2-fluoro-5-hydroxyphenyl)-1H-isoindole-1,3(2H)-dione
  • 2,6-Dibromo-4-cyanophenyl pentanoate
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