Online Database of Chemicals from Around the World

Dibucaine hydrochloride
[CAS# 61-12-1]

List of Suppliers
Jinan Chenghui-Shuangda Chemical Co., Ltd. China Inquire  
+86 (531) 5889-7051
+86 15053146086
jnchsd@qq.com
QQ chat
Chemical manufacturer since 2002
chemBlink standard supplier since 2007
BOC Sciences USA Inquire  
+1 (631) 485-4226
info@bocsci.com
Chemical manufacturer
chemBlink standard supplier since 2010
Jinan An-dm Chemical Co., Ltd. China Inquire  
+86 15550736712
andmchem@hotmail.com
Chemical manufacturer
chemBlink standard supplier since 2014
Chongqing Land Tower Pharmaceutical Co., Ltd. China Inquire  
+86 (23) 6898-0308
business@cqlandtower.com
Chemical manufacturer since 2010
chemBlink standard supplier since 2014
Hangzhou Leap Chem Co., Ltd. China Inquire  
+86 (571) 8771-1850
market19@leapchem.com
QQ chat
Chemical manufacturer since 2006
chemBlink standard supplier since 2015
Typu Group China Inquire  
+86 85220966
order@typugroup.com
Chemical distributor since 2008
chemBlink standard supplier since 2021
Shandong Chenghui Shuangda Pharmaceutical Co., Ltd. China Inquire  
+86-531-58897029
ericqiao@jnchsd.com
QQ chat
WeChat: 15550412551
WhatsApp: 15550412551
Chemical manufacturer since 2014
chemBlink standard supplier since 2025
Toronto Research Chemicals Inc. Canada Inquire  
+1 (416) 665-9696
info@trc-canada.com
Chemical manufacturer since 1982
Complete supplier list of Dibucaine hydrochloride
Identification
Classification API >> Anesthetic agents >> Local anesthetics
Name Dibucaine hydrochloride
Synonyms 2-Butoxy-N-[2-(diethylamino)ethyl]-4-quinolinecarboxamide monohydrochloride; 2-Butoxy-N-(2-diethylaminoethyl)cinchoninamide hydrochloride
Molecular Structure CAS # 61-12-1, Dibucaine hydrochloride, 2-Butoxy-N-[2-(diethylamino)ethyl]-4-quinolinecarboxamide monohydrochloride, 2-Butoxy-N-(2-diethylaminoethyl)cinchoninamide hydrochloride
Molecular Formula C20H29N3O2.HCl
Molecular Weight 379.93
CAS Registry Number 61-12-1
EC Number 200-498-1
SMILES CCCCOC1=NC2=CC=CC=C2C(=C1)C(=O)NCCN(CC)CC.Cl
Properties
Melting point 99 - 101 ºC (Expl.)
Solubility DMSO 76 mg/mL, Water 76 mg/mL (Expl.)
Safety Data
Hazard Symbols symbol symbol symbol   GHS05;GHS07;GHS09 Danger    Details
Hazard Statements H302-H317-H318-H411    Details
Precautionary Statements P261-P264-P264+P265-P270-P272-P273-P280-P301+P317-P302+P352-P305+P354+P338-P317-P321-P330-P333+P317-P362+P364-P391-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Serious eye damageEye Dam.1H318
Acute toxicityAcute Tox.4H302
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
Skin sensitizationSkin Sens.1H317
Acute toxicityAcute Tox.3H301
Acute toxicityAcute Tox.3H311
Skin irritationSkin Irrit.2H315
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Acute toxicityAcute Tox.2H330
Specific target organ toxicity - single exposureSTOT SE3H335
Acute hazardous to the aquatic environmentAquatic Acute1H400
SDS Available
up Discovory and Applicatios
Dibucaine hydrochloride is a potent local anesthetic belonging to the amide class of anesthetics. It is primarily used for topical anesthesia of the skin and mucous membranes and occasionally in small doses for spinal anesthesia. Dibucaine hydrochloride exerts its anesthetic effect by blocking voltage-gated sodium channels in nerve cell membranes, thereby inhibiting the initiation and propagation of nerve impulses and causing a reversible loss of sensation in the area of application.

The compound was developed and introduced into clinical use in the mid-20th century, with its chemical structure designed to provide strong and long-lasting local anesthesia. Dibucaine hydrochloride is noted for its high potency compared to other local anesthetics, which makes it effective in very small amounts. It is commonly supplied as a hydrochloride salt to enhance its solubility and stability in aqueous formulations.

Clinically, dibucaine hydrochloride is often used in topical creams, ointments, or solutions for the relief of pain, itching, and discomfort associated with conditions such as hemorrhoids, minor burns, insect bites, and anal fissures. Its use in spinal anesthesia is limited due to concerns about neurotoxicity when used in higher concentrations or volumes.

Pharmacodynamically, dibucaine blocks the conduction of nerve impulses by selectively binding to and stabilizing the inactive state of sodium channels on neuronal membranes. This action prevents the influx of sodium ions necessary for depolarization, effectively blocking nerve signal transmission.

Pharmacokinetically, dibucaine hydrochloride is absorbed slowly from topical sites, which contributes to its prolonged duration of action. When absorbed systemically, it is metabolized primarily in the liver by enzymatic hydrolysis and N-dealkylation pathways. The metabolites and unchanged drug are excreted mainly via the kidneys. The elimination half-life varies depending on the route of administration but is generally several hours.

Adverse effects are primarily related to local irritation or allergic reactions at the site of application. Systemic toxicity is rare but can occur if excessive amounts are absorbed or injected, potentially causing symptoms such as dizziness, tinnitus, nervousness, seizures, or cardiac disturbances. Due to its potency, careful dosing and application are important to avoid toxicity.

Dibucaine hydrochloride is also known for its use in the dibucaine number test, a diagnostic assay to measure atypical plasma cholinesterase activity, which helps identify individuals with genetic variants that affect the metabolism of certain anesthetics.

In summary, dibucaine hydrochloride is a highly potent local anesthetic used primarily for topical pain relief. Its mechanism of action involves sodium channel blockade leading to nerve impulse inhibition. The compound’s strong anesthetic effect, coupled with a relatively slow systemic absorption and metabolism, allows for prolonged local anesthesia with a generally favorable safety profile when used appropriately.

References

1974. Kinetic characteristics of monoamine oxidase and serum cholinesterase in several related rat strains. Biochemical Genetics, 11(4).
DOI: 10.1007/bf00485998

2018. Greenness assessment as per Eco-scale and AMVI metrics for the chromatographic assay of selected drugs in a semisolid dosage form and in tissues. Chemical Papers, 73(3).
DOI: 10.1007/s11696-018-0619-z

2022. A quantitative high-throughput screen identifies compounds that lower expression of the SCA2-and ALS-associated gene ATXN2. The Journal of Biological Chemistry, 298(8).
DOI: 10.1016/j.jbc.2022.102228
Market Analysis Reports
List of Reports Available for Dibucaine hydrochloride
Related Products
1,1'-Dibutylferrocene  N,N-Dibutylformamide  Dibutyl fumarate  Dibutylgermanium dichloride  4,5-Dibromo-o-xylene  2,5-Dibromo-m-xylene  alpha,alpha'-Dibromo-p-xylene-4,4'-difluorodiphenyl sulfone-4,4'-thiobisbenzenethiol copolymer  Dibromo zinc bis[3-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]phenyl]porphyrin  Dibromo zinc bis[3-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]phenyl]porphyrin-ethinyl dimer  2,3-Dibromo-1-propanol  Dibunate sodium  9,10-Dibutoxyanthracene  3,6-Dibutoxy-1,2-benzenedicarbonitrile  2,5-Dibutoxy-4-morpholinobenzenediazonium chlorozincate  1,4-Dibutoxy-2,3-naphthalenedicarbonitrile  [(2,5-Dibutoxy-1,4-phenylene)bis(methylene)]bis[triphenylphosphonium] dibromide  Dibutoxypropylborane  Dibutoxytitanium bis(ethyl acetoacetate)  1,1-Dibutoxytrimethylamine  N,N-Dibutylacetamide