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Ibutilide Hemifumarate

HCID 6437366
NotesReactions
Basic informationNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
122647-32-9
Standard SMILES
CCCCCCCN(CC)CCCC(O)c1ccc(NS(C)(=O)=O)cc1.O=C(O)/C=C/C(=O)O
InChIKey
PAXBPNBQGZYWHP-WLHGVMLRSA-N
Molecular formula
C24H40N2O7S
Average molar mass
500.7 g/mol
Monoisotopic mass
500.25562279

Names & identifiers

Preferred name
Ibutilide Hemifumarate
IUPAC
(E)-but-2-enedioic acid;N-[4-[4-[ethyl(heptyl)amino]-1-hydroxybutyl]phenyl]methanesulfonamide
English name
Ibutilide fumarate
Molecular formula
(C20H36N2O3S)2.C4H4O4
Molecular weight
885.24

Names & synonyms

RefChem:789647687-381-2Ibutilide Hemifumarate(2E)-but-2-enedioic acid; N-(4-{4-[ethyl(heptyl)amino]-1-hydroxybutyl}phenyl)methanesulfonamide1217204-74-4SCHEMBL1649397HY-B0387RIbutilide (fumarate) (Standard)EBC-29022PD052226EN300-21702894SR-01000942241
Show more names
D00648Corvert (tn)Corvert FumarateIbutilide fumarateIBUTILIDE FUMRTATEIbutibide FumarateIbulitide fumarateIbutilide 1/2FumarateIbutilideHemifumarate>
SR-01000942241-1(E)-2-butenedioic acid; N-[4-[4-[ethyl(heptyl)amino]-1-hydroxybutyl]phenyl]methanesulfonamide

Database identifiers

CAS
122647-32-9
PubChem CID
6437366

Properties

Computed structural properties

Topological polar surface area
153 Ų
Hydrogen bond donors
4
Hydrogen bond acceptors
9
Rotatable bonds
16
Heavy atoms
34
Formal charge
0
Complexity
561

Physicochemical properties

Melting point
112 · 112-117C
RTECS
475700 · PB0475700
storage temp.
2 · 2-8°C
solubility
2 O: · H2O: >20mg/mL
form
solid
color
off-white to tan
Water Solubility
2 O: · H2O: >20mg/mL
λmax
267 nm · 267nm(EtOH)(lit.)
Merck
14 · 14,4883
InChIKey
PCIOHQNIRPWFMV-WXXKFALUSA-N
SMILES
C1(=CC=C(NS(=O)(=O)C)C=C1)C(O)CCCN(CC)CCCCCCC.C1(C(O)CCCN(CC)CCCCCCC)C=CC(NS(=O)(=O)C)=CC=1.C(/C(=O)O)=C\C(=O)O
CAS DataBase Reference
122647 · 122647-32-9(CAS DataBase Reference)
FDA UNII
9 L5X4M5L6I · 9L5X4M5L6I
UNSPSC Code
41116107 · 41116107
NACRES
77 · NA.77
Symbol(GHS)
7 · GHS07,GHS08
Signal word

Safety & regulation

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

Safety data

wgk
1
hs_code
2935904000
Toxicity
rat,LD,oral,> 500mg/kg (500mg/kg),Teratology, The International Journal of Abnormal Development. Vol. 49, Pg. 406, 1994.
risk_code
22
Signal word
Warning
Symbol(GHS)
GHS07,GHS08
hazard_code
Xn
Storage Class
11 - Combustible Solids
Hazard statements
H302-H361d
Hazard Classifications
Acute Tox. 4 OralRepr. 2
Precautionary statements
P202-P264-P270-P280-P301+P312-P308+P313

Chemistry & industry

Applications · 3 items

DescriptionCovert was launched in the US and UK for treatment of atrial fibrillation and flutter and can be synthesized in three steps from N-phenyl rnethanesulfonamide. While ibutilide has an asymmetric center, it has been determined that the racemate is equipotent with either enantiomer. The antiarrhythmic action is derived from the compounds ability to prolong the action potential duration and lengthen the refractory period of myocardial tissue. Class Ⅲ antiarrhythrnic agents accomplish this by blocking outward potassium channels, however, ibutilide elicits the same effect by activation of slow inward sodium channels. Recent evidence indicates that it also is a potent blocker of the rapidly acting delayed rectifier potassium current (lkr)and may block the ATP-inhibited potassium channel.

Description(±)-Ibutilide is a class III antiarrhythmic agent. It inhibits the rapidly activating delayed-rectifier potassium current (IKr) in AT-1 myocytes with an IC50 value of 20 nM. (±)-Ibutilide also enhances the late inward sodium current (INa) and increases the action potential duration in isolated guinea pig ventricular cells. It decreases ventricular fibrillation induced by the ATP-dependent potassium channel activator pinacidil in Langendorff isolated perfused rabbit hearts when used at concentrations ranging from 3 to 30 μM. (±)-Ibutilide (15 μg/kg, i.v.) increases the effective refractory period (ERP) of the left and right atrium in anesthetized pigs. It prevents rapid pacing-induced atrial flutter in dogs when administered orally at doses ranging from 0.25 to 5 mg/kg. Formulations containing ibutilide have been used in the treatment of atrial arrhythmias.

UsesA methanesulfonanilide antiarrhythmic agent; prologns myocardial action potential duration, predominantly by activation of slow inward sodium current. Antiarrhythmic (class III).

Upstream & downstream products

Upstream raw materials

Lithium Aluminum HydrideAnilinePotassium sodium tartrateMethanesulfonyl chloride

Related reactions

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New reaction record

No reaction records under the current filter.

Compound notes

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On this pageBasic informationNames & identifiersPropertiesSafety & regulationChemistry & industryRelated reactionsCompound notes
Warning
Hazard statements
302 · H302-H361d
Precautionary statements
202 · P202-P264-P270-P280-P301+P312-P308+P313
Hazard Codes
Xn
Risk Statements
22 · 22
WGK Germany
1 · 1
HS Code
2935904000 · 2935904000
Storage Class
11 · 11 - Combustible Solids
Hazard Classifications
4 OralRepr · Acute Tox. 4 OralRepr. 2
Toxicity
500 mg/kg · rat,LD,oral,> 500mg/kg (500mg/kg),Teratology, The International Journal of Abnormal Development. Vol. 49, Pg. 406, 1994.
Fumaric acid
Succinic anhydride
ethylheptylamine
1-Hydroxybenzotriazole

Suppliers100 total

梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
南通飞宇生物科技有限公司0513-68819626 15152877458 · [email protected]
济南百隆化学有限公司[email protected] · [email protected]
成都超九八生物科技有限公司13348960310 13348960310 · [email protected]
合肥翰刚医药科技有限公司+8618062405514 · [email protected]
广州隽沐生物科技股份有限公司020-36607679; 13502246435 · [email protected]
Dayang Chem (Hangzhou) Co.,Ltd.+86-0571-88938639 17705817739 · [email protected]
上海钰源生物化学有限公司021-13814116 13814116708 · [email protected]
LGM Pharma1-(800)-881-8210 · [email protected]
江西瑞威尔生物科技有限公司400-880-2824 18107960669 · [email protected]
江西瑞威尔生物科技有限公司18502728206 · [email protected]
江西瑞威尔生物科技有限公司18502762009 · [email protected]
阿法埃莎(中国)化学有限公司400-6106006 · [email protected]
南京圣亿来化工有限公司19951936396 · [email protected]
西安泽邦生物科技有限公司[email protected]
MedBio脉铂医药021-69568360 18916172912 · [email protected]
浙江九旭药业有限公司[email protected]
Pure Chemistry Scientific Inc.001-857-928-2050 or 1-888-588-9418 · [email protected]
上海泰坦科技股份有限公司4006009262 13023226327 · [email protected]
MedChemexpress LLC021-58955995 · [email protected]
BOC Sciences1-631-485-4226; 16314854226 · [email protected]
AdooQ BioScience, LLC+1 (866) 930-6790 · [email protected]
TCI AMERICA800-4238616 · [email protected]
TOKYO CHEMICAL INDUSTRY CO., LTD.03-36680489 · [email protected]
TCI Europe320-37350700 · [email protected]
广州爱纯医药科技有限公司020-39119399 18927568969 · [email protected]
南京生利德生物科技有限公司025-57798810 18652991625 · [email protected]
苏州亚科科技股份有限公司0512-87182055 13451648594 · [email protected]
湖北鑫源顺医药化工有限公司13971561712, 13995564702, 027-50664929 · [email protected]
HBCChem, Inc.+1-510-219-6317 · [email protected]
天津普西唐生物医药科技有限公司010-60605840 · [email protected]
南京百鑫德诺生物科技有限公司025-58849295 · [email protected]
上海孚一生物科技有限公司+86 (21) 61124340
凯试(上海)科技有限公司021-50135380 · [email protected]
湖北巨胜科技有限公司027-59599241 18871490274 · [email protected]
池州凯隆进出口贸易有限公司[email protected]
Sigma-Aldrich西格玛奥德里奇(上海)贸易有限公司021-61415566 800-8193336 · [email protected]
深圳振强药物研发有限公司+86-0755-66853366 +86-13670046396 · [email protected]
上海泽涵生物医药科技有限公司021-61350663 13052117465 · [email protected]
TargetMol中国(陶术生物)021-021-33632979 15002134094 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354; +1-00000000000 · [email protected]
湖北威德利化学科技有限公司027-83989310 18627915365 · [email protected]
湖北威德利化学试剂有限公司18327179646 · [email protected]
西安美川生物科技有限公司029-89275612 +8618991951683 · [email protected]
武汉鑫儒化工有限公司15927387915 15337108568 · [email protected]
安耐吉化学&3A(安徽泽升科技股份有限公司)400-0056266 · [email protected]
武汉多普乐生物医药有限公司+86-02787215551 19945035818 · [email protected]
上海珞珐生化科技有限公司021-51111890 15317326293 · [email protected]
EMMX Biotechnology LLC888-539-0666 · [email protected]

Additional notes

DefinitionChEBI: Ibutilide fumarate is a member of benzenes and an organic amino compound.