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Diphemanil methyl sulfate

HCID 6126
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Basic information

CAS
62-97-5
Standard SMILES
COS(=O)(=O)[O-].C[N+]1(C)CCC(=C(c2ccccc2)c2ccccc2)CC1
InChIKey
BREMLQBSKCSNNH-UHFFFAOYSA-M
Molecular formula
C20H24N.CH3O4S
Average molar mass
389.5 g/mol
Monoisotopic mass
389.16607952

Overview

Diphemanil methylsulfate is the alkene resulting from the formal Wittig olefination of benzophenone and 1,1-dimethyl-4-bromopiperidinium methylsulfate. A quaternary ammonium anticholinergic, it binds muscarinic acetycholine receptors and thereby decreases secretory excretion of stomach acids, saliva and sweat, It is used topically in the treatment of hyperhidorsis (excessive sweating). It has a role as a bronchodilator agent, a muscarinic antagonist and a parasympatholytic. It is a member of piperidines and a quaternary ammonium salt.

Names & identifiers

Preferred name
Diphemanil methyl sulfate
IUPAC
4-benzhydrylidene-1,1-dimethylpiperidin-1-ium;methyl sulfate
English name
Diphemanil Methylsulfate
Molecular formula
C20H24N.CH3O4S
Molecular weight
389.51

Names & synonyms

DIPHEMANIL METHYLSULFATE62-97-5Diphemanil metilsulfateDiphemanil methosulfateDiphemanil methylsulphateMetilsulfate de diphemanilMetilsulfato de difemaniloDiphemanili metilsulfasDiphemanil methyl sulfateDTXSID9022948W2ZG23MGYI4-(Diphenylmethylene)-1,1-dimethylpiperidinium methyl sulfate
Show more names
diphemanilprantalvaritonTalprandemotilnivelonadiphenatilvagophemanildiphenmethanilDiphemanil mesylate
NSC-41725N,N-Dimethyl-4-piperidylidene-1,1-diphenylmethane methylsulfatep-(alpha-Phenylbenzylidene)-1,1-dimethylpiperidinium methyl sulfatePiperidinium, 4-(diphenylmethylene)-1,1-dimethyl-, methyl sulfateDTXCID402948CHEBI:59782diphAmanil (cation)difemanile metilsolfato

Database identifiers

CAS
62-97-5

Properties

Computed structural properties

Topological polar surface area
74.8 Ų
Hydrogen bond donors
0
Hydrogen bond acceptors
4
Rotatable bonds
2
Heavy atoms
27
Formal charge
0
Complexity
426

Experimental & physicochemical properties

Human Drugs · 2 items

FDA approved drugs -> Active ingredient

FDA approved drugs -> Active ingredient

Physicochemical properties

Melting point
194 · 194-195℃
storage temp.
-20 °C · Inert atmosphere,Store in freezer, under -20°C
Water Solubility
Soluble in water
solubility
16.67 mg/mL · : 16.67 mg/mL (42.80 mM; Need ultrasonic)
form
powder to crystal
color
White to Almost white
Stability
Hygroscopic
EWG's Food Scores
1 · 1
FDA UNII
2 ZG23MGYI · W2ZG23MGYI
ATC code
3 AB15 · A03AB15
Symbol(GHS)
7 · GHS07
Signal word
Warning
Hazard statements
302 · H302-H315-H319

Safety & regulation

Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.

GHS classification

GHS Classification · 4 items

Danger

H301 (93.1%): Toxic if swallowed [Danger Acute toxicity, oral]

P260, P264, P264+P265, P270, P271, P280, P284, P301+P316, P304+P340, P305+P354+P338, P316, P317, P320, P321, P330, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 29 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Hazard information

Regulatory Information · 2 items

Chemical: Piperidinium, 4-(diphenylmethylene)-1,1-dimethyl-, methyl sulfate

Piperidinium, 4-(diphenylmethylene)-1,1-dimethyl-, methyl sulfate: Does not have an individual approval but may be used under an appropriate group standard

Other Safety InformationEvaluation - Chemicals not considered for in depth evaluation - Not commercially active in Australia
Hazard Classes and CategoriesAcute Tox. 3 (93.1%)

Safety data

hs_code
2933.39.4100
Toxicity
LD50 in rats, mice, guinea pigs (mg/kg): 1107, 64, 404 orally (Margolin)
Signal word
Warning
Symbol(GHS)
GHS07
Hazard statements
H302-H315-H319
Precautionary statements
P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Chemistry & industry

Pharmacology

MeSH Pharmacological Classification · 2 items

Agents that cause an increase in the expansion of a bronchus or bronchial tubes.

Agents that inhibit the actions of the parasympathetic nervous system. The major group of drugs used therapeutically for this purpose is the MUSCARINIC ANTAGONISTS.

Applications · 4 items

DescriptionDiphemanil is a quaternary ammonium anticholinergic agent. It induces relaxation of isolated guinea pig trachea strips precontracted with methacholine (EC50 = 0.12 nM). Diphemanil reverses increases in lung resistance and decreases in dynamic lung compliance induced by the non-selective acetylcholine receptor agonist carbachol (carbamoylcholine; ) in vagotomized cats (ED50s = 17.5 and 19.3 μg/kg, respectively). It reduces salivation induced by the muscarinic acetylcholine receptor agonist pilocarpine in mice when administered subcutaneously at doses ranging from 1.25 to 10 mg/kg.

UsesDiphemanil Methosulfate is an anticholinergic agent; a synthetic quaternary ammonium compound with anitmuscarinic properties used in the treatment of Frey''s syndrome and is used as a parasympatholytic bronchodilator agent.

UsesBronchodilatator;Anticholinergic

General DescriptionDiphemanil methylsulfate,4-(diphenylmethylene)-1,1-dimethylpiperidiniummethylsulfate (Prantal), or diphemanil methylsulfate is apotent cholinergic blocking agent. In the usual dosagerange, it acts as an effective parasympatholytic by blockingnerve impulses at the parasympathetic ganglia, but it doesnot invoke a sympathetic ganglionic blockade. It is claimedto be highly specific in its action on those innervations thatactivate gastric secretion and GI motility. Although thisdrug can produce atropine-like side effects, they rarelyoccur at recommended doses. The highly specific nature ofits action on gastric functions makes the drug useful inthe treatment of peptic ulcer, and its lack of atropine-likeeffects makes its use much less distressing than other antispasmodicdrugs. In addition to its action in decreasinggastric hypermotility, diphemanil methylsulfate is valuablein hyperhidrosis in low doses (50 mg twice daily) or topically.The drug is not well absorbed from the GI tract,particularly in the presence of food, and should be administeredbetween meals. The methylsulfate salt was chosen asthe best, because the chloride is hygroscopic and the bromideand iodide ions have exhibited toxic manifestations inclinical use.

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Compound notes

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On this pageBasic informationOverviewNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
PubChem CID
6126
DTXSID
DTXSID9022948
ChEMBL
CHEMBL1200880
ChEBI
CHEBI:59782
UNII
W2ZG23MGYI
EC Number
200-552-4
Precautionary statements
501 · P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330
HS Code
2933.39 · 2933.39.4100
Toxicity
50 in · LD50 in rats, mice, guinea pigs (mg/kg): 1107, 64, 404 orally (Margolin)

Upstream & downstream products

Upstream raw materials

Dimethyl sulfateSulfuric acidMagnesiumBromobenzene4-benzoyl-N-methylpiperidine
Additional notes · 1 item

DefinitionChEBI: The alkene resulting from the formal Wittig olefination of benzophenone and 1,1-dimethyl-4-bromopiperidinium methylsulfate. A quaternary ammonium anticholinergic, it binds muscarinic acetycholine receptors and thereby decreases secretory excretion of stoma h acids, saliva and sweat, It is used topically in the treatment of hyperhidorsis (excessive sweating).