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Otilonium bromide

Otilonium bromide Structure
CAS No.
26095-59-0
Chemical Name:
Otilonium bromide
Synonyms
Otilonium;OCTYLONIUM BROMIDE;Spasmomen;SPASMONEN;SP-63;Spasen;Doralin;Menoctyl;Pasminox;Spasmome
CBNumber:
CB6712880
Molecular Formula:
C29H43BrN2O4
Molecular Weight:
563.58
MOL File:
26095-59-0.mol
MSDS File:
SDS
Modify Date:
2024/6/3 18:47:13

Otilonium bromide Properties

Melting point 130-133°C
storage temp. -20°C
solubility DMSO (Slightly), Methanol (Slightly)
form powder
color white to beige
CAS DataBase Reference 26095-59-0(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P305+P351+P338
Toxicity LD50 in mice (mg/kg) 87.0 i.p.
NFPA 704
0
1 0

Otilonium bromide price More Price(2)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) SML1454 Otilonium bromide ≥98% (HPLC) 26095-59-0 5MG ₹10792.53 2022-06-14 Buy
Sigma-Aldrich(India) SML1454 Otilonium bromide ≥98% (HPLC) 26095-59-0 25MG ₹43505.68 2022-06-14 Buy
Product number Packaging Price Buy
SML1454 5MG ₹10792.53 Buy
SML1454 25MG ₹43505.68 Buy

Otilonium bromide Chemical Properties,Uses,Production

Description

Otilonium is an inhibitor of L-type (IC50 = 2.3 μM) and T-type calcium channels (IC50s = 0.8, 1.1, and 0.4 μM for Cav3.1, Cav3.2, and Cav3.3, respectively). It is also an antagonist of muscarinic acetylcholine receptors (mAChRs; IC50s = 0.054, 0.4, 0.222, and 0.156 μM for M1, M2, M4, and M5 muscarinic receptors, respectively) and the platelet activating factor (PAF) receptor (IC50 = 0.0552 μM). Otilonium inhibits the inward calcium current in isolated rat colonic smooth muscle cells (EC50 = 885 nM), an effect that can be blocked by the L-type calcium channel inhibitor nifedipine . It inhibits contractions induced by the muscarinic acetylcholine receptor (mAChR) agonist methacholine in isolated circular muscle of the guinea pig proximal colon (IC50 = 3.7 μM). Otilonium (4 mg/kg) decreases fecal excretion and wet dog shakes and increases the tail withdrawal latency in the tail-flick test in a rat model of opioid withdrawal syndrome induced by morphine and naloxone.

Chemical Properties

White Powder

Uses

Otilonium bromide is an antimuscarinic

General Description

Otilonium bromide is an antispasmodic. It contains a red color ACh (acetylcholine) like moiety bound to an aromatic system that ends with an octyl ether.

Safety Profile

Poison by intraperitoneal route. Moderately toxic by ingestion and subcutaneous routes. When heated to decomposition it emits toxic fumes of Brí and NOx.

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Otilonium bromide Spectrum

Menoctyl N,N-Diethyl-N-methy-2-[[4-[[2-(octyloxy)benzoyl]amino]benzoyl]oxy]ethanaminium Bromide Pasminox SP-63 Spasen Spasmoctyl Spasmome OTYLONIUMBROMIDE diethyl-methyl-[2-[4-[(2-octoxybenzoyl)amino]benzoyl]oxyethyl]azanium bromide Aotixiuan OtioniuM BroMide OtiloniuM broMide(OctyloniuM broMide) Octylonium IodideDiscontinued See: O293250 Ethanaminium, N,N-diethyl-N-methyl-2-[[4-[[2-(octyloxy)benzoyl]amino]benzoyl]oxy]-, bromide (1:1) ammonium,diethyl(2-hydroxyethyl)methyl-,bromide,p-(o-(octyloxy)benzamido)ben diethyl(2-hydroxyethyl)methylammoniumbromidep-(o-(octyloxy)benzamido)benzoa ethanaminium,n,n-diethyl-n-methyl-2-((4-((2-(octyloxy)benzoyl)amino)benzoyl) octylonium ottiloniobromuro n,n-diethyl-n-methyl-2-((4-((2-(octyloxy)benzoyl)amino)benzoyl)oxy)-ethanaminium bromide OCTYLONIUM IODIDE otilonium bromide diethyl(2-hydroxyethyl) methylammonium bromide p-(o-(octyloxy)benzamido)-benzoate Doralin diethyl-[2-[[4-[[(2-heptoxyphenyl)-oxomethyl]amino]phenyl]-oxomethoxy]ethyl]-methylammonium bromide aoixijan DORALIN;OCTYLONIUM BROMIDE;SP63;SPASMOMEN Otilonium bromide USP/EP/BP Otilonium bromideQ: What is Otilonium bromide Q: What is the CAS Number of Otilonium bromide Q: What is the storage condition of Otilonium bromide Otilonium Spasmomen OCTYLONIUM BROMIDE SPASMONEN Isoleucine Impurity 14 26095-59-0 C29H43BrN2O4 C29H43IN2O4 C29H43N2O4Br BrC29H43N2O4 Inhibitors Intermediates & Fine Chemicals Pharmaceuticals