Bitolterol
Also known as Bitolterolum, Benzoic acid, 4-methyl-, 4-(2-((1,1-dimethylethyl)amino)-1-hydroxyethyl)-1,2-phenylene ester, 4-(2-(tert-butylamino)-1-hydroxyethyl)-o-phenylene di-p-toluate
Key facts
What buyers check first
- CAS number
- 30392-40-6
- Formula
- C28H31NO5
- Molar mass
- 461.56 g/mol
- HS code
- 292250
- Category
- Respiratory, allergy and digestive drugs
What is Bitolterol?
Plain description, key identifiers and synonyms
Bitolterol is the di-4-toluate ester of (+-)-N-tert-butylnoradrenaline (colterol). A pro-drug for colterol, a beta2-adrenergic receptor agonist, bitolterol is used as its methanesulfonate salt for relief of bronchospasm in conditions such as asthma, chronic bronchitis and emphysema. It has a role as a beta-adrenergic agonist, a bronchodilator agent, an anti-asthmatic drug and a prodrug. It is a member of ethanolamines, a carboxylic ester, a secondary alcohol, a secondary amino compound and a diester.
Identifiers
Registry numbers, names and line notations, tap to copy
- IUPAC name
- [4-[2-(tert-butylamino)-1-hydroxyethyl]-2-(4-methylbenzoyl)oxyphenyl] 4-methylbenzoate
- CAS number
- 30392-40-6 CAS number cross-checked
- Molecular formula
- C28H31NO5
- UNII
- 9KY0QXD6LI
- InChIKey
- FZGVEKPRDOIXJY-UHFFFAOYSA-N
- InChI
- InChI=1S/C28H31NO5/c1-18-6-10-20(11-7-18)26(31)33-24-15-14-22(23(30)17-29-28(3,4)5)16-25(24)34-27(32)21-12-8-19(2)9-13-21/h6-16,23,29-30H,17H2,1-5H3
- SMILES (canonical and isomeric)
- CC1=CC=C(C=C1)C(=O)OC2=C(C=C(C=C2)C(CNC(C)(C)C)O)OC(=O)C3=CC=C(C=C3)C
Synonyms
- Bitolterolum
- Benzoic acid, 4-methyl-, 4-(2-((1,1-dimethylethyl)amino)-1-hydroxyethyl)-1,2-phenylene ester
- 4-(2-(tert-butylamino)-1-hydroxyethyl)-o-phenylene di-p-toluate
- 4-[2-(tert-Butylamino)-1-hydroxyethyl]-o-phenylene di-p-toluate
- bis(4-methylbenzoic acid) 4-[2-(tert-butylamino)-1-hydroxyethyl]-1,2-phenylene ester
- bitolterolo
- bis(4-methylbenzoic acid) 4-(2-(tert-butylamino)-1-hydroxyethyl)-1,2-phenylene ester
- 5-(2-(tert-butylamino)-1-hydroxyethyl)-2-(4-methylbenzoyloxy)phenyl 4-methylbenzoate
- [4-[2-(tert-butylamino)-1-hydroxyethyl]-2-(4-methylbenzoyl)oxyphenyl] 4-methylbenzoate
- WIN 32784
- Bitolterol (INN)
- Benzoic acid, 4-methyl-, 1,1'-[4-[2-[(1,1-dimethylethyl)amino]-1-hydroxyethyl]-1,2-phenylene] ester
- 4-(2-(tert-butylamino)-1-hydroxyethyl)-1,2-phenylene bis(4-methylbenzoate)
- p-Toluic acid, 4-[2-(tert-butylamino)-1-hydroxyethyl]-o-phenylene ester, S 1540
- Bitolterol-API
- 4-[2-(tert-Butylamino)-1-hydroxyethyl]-1,2-phenylene bis(4-methylbenzoate)
- 4-(2-(tert-Butylamino)-1-hydroxyethyl-o-phenylene di-p-toluate
- 4-(2-(tert-Butylamino)-1-hydroxyethyl-1,2-phenylen di-4-toluat
- alpha((tert-butylamino)methyl)-3,4-dihydroxybenzyl alcohol 3,4-di-p-toluate
- 4-[2-(tert-Butylamino)-1-hydroxyethyl]-2-[(4-methylbenzoyl)oxy]phenyl 4-methylbenzoate #
- 4-[2-(tert-butylamino)-1-hydroxyethyl]benzene-1,2-diyl bis(4-methylbenzoate)
- 4-{2-[(1,1-dimethylethyl)amino]-1-hydroxyethyl}benzene-1,2-diyl bis(4-methylbenzoate)
Physical and chemical properties
Measured values and descriptors computed from the structure
Physical and chemical properties
Measured values, check the supplier specification for your grade
No measured properties are recorded for this substance yet. Ask suppliers for a technical data sheet.
Values vary by grade. Ask suppliers for the COA or TDS of the batch you buy.
Computed descriptors
Calculated from the structure, useful for screening and formulation
| Molecular weight | 461.56 g/molcalc.Computed value |
|---|---|
| Exact mass | 461.2202 Dacalc.Computed value |
| LogP (octanol/water) | 5.16calc.Computed value |
| Topological polar surface area | 84.86 Ųcalc.Computed value |
| Hydrogen bond donors | 2calc.Computed value |
| Hydrogen bond acceptors | 6calc.Computed value |
| Rotatable bonds | 7calc.Computed value |
| Heavy atoms | 34calc.Computed value |
| Rings | 3calc.Computed value |
| Aromatic rings | 3calc.Computed value |
| Fraction sp3 carbons | 0.29calc.Computed value |
| Formal charge | 0calc.Computed value |
| Stereocentres | 1calc.Computed value |
| Lipinski rule of five | Passes (1 violation)calc.Computed value |
Calculated for screening. Confirm critical figures with the supplier.
Murcko scaffold
The ring system that remains when every side chain is removed
O=C(Oc1ccccc1OC(=O)c1ccccc1)c1ccccc1
3 rings, 24 atoms, the o-Phenylene dibenzoate ring system.
19 other chemicals share this scaffoldSafety and hazards
GHS classification summary, not a safety data sheet
No GHS hazard classification is recorded for this substance yet. That does not mean it is harmless.
GHS classification summary, not a safety data sheet (SDS). Classifications can differ by supplier, grade and concentration. Always check the supplier's SDS.
Bitolterol suppliers
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Bitolterol price
Indicative price range per kg from live supplier offers
Suppliers quote this chemical on request. Send one free request and compare quotes side by side.
Uses and applications
What the substance is used for, by industry and function
Industries and functions
Pharmacological actions
- Adrenergic beta-2 Receptor Agonists
- Bronchodilator Agents
Roles
- adrenergic agent
- adrenergic agonist
- anti-asthmatic agent
- anti-asthmatic drug
- beta-adrenergic agonist
- beta-adrenergic drug
- bronchodilator agent
- neurotransmitter agent
- pharmaceutical
- pro-agent
- prodrug
Pharmacology
Bitolterol is a diester sympathomimetic amine with bronchodilator activity. As an ester prodrug, bitolterol is hydrolyzed by esterases to its active metabolite colterol (N-t-butylarterenol). Colterol selectively binds to and activates beta-2 adrenergic receptors in bronchiolar smooth muscle, thereby causing stimulation of adenyl cyclase, the enzyme that catalyzes the conversion of adenosine triphosphate (ATP) to cyclic-3',5'-adenosine monophosphate (cAMP). Increased intracellular cAMP levels cause relaxation of bronchial smooth muscle. This increases air flow and prevents bronchospasms and may eventually lead to an improvement of airway function.
Regulatory status
Inventories, regulations and trade controls that list this substance
No regulatory list memberships are recorded for this substance yet. Always check the rules of the importing and exporting country before trade.
HS code and trade data
Customs classification and reported world trade statistics
Global trade
World import and export statistics for the HS code Bitolterol is traded under.
Amino-alcohol-phenols, amino-acid-phenols and other amino-compounds with oxygen function
- China39.2%
- United Kingdom27.1%
- India * partner reported4.8%
- United States20.7%
- Germany7.6%
- Italy6.6%
* Partner reported figures, a lower bound.
The HS code shown for Bitolterol is indicative (it was assigned by structure rules). Confirm the classification with your customs broker before shipping.
Frequently asked questions
Quick answers about Bitolterol, based on the data on this page
What is Bitolterol?
What is the CAS number of Bitolterol?
What is the molecular formula and weight of Bitolterol?
What is Bitolterol used for?
Is Bitolterol hazardous?
What is the HS code of Bitolterol?
Where can I buy Bitolterol?
What is the price of Bitolterol?
Guides for buyers
Practical guides that help when you source, ship or handle Bitolterol
- Article, QualityPharma grades explained: IP vs BP vs USP vs EPWhat the Indian, British, US and European pharmacopoeias are, how their monographs differ, what multi grade claims mean and why a grade alone does not make a product fit for medicines.Read
- Article, SourcingHow to write an RFQ that gets fast and accurate quotesWhat suppliers need to quote quickly and comparably: exact product identity, quantity and packing, delivery terms, documents, samples and payment, with a ready to use template.Read
- Guide, Trade and logisticsHS codes for chemicals and why they matterHow the Harmonized System classifies chemicals, the chapters that matter, the rules for chemically defined compounds and mixtures, and practical steps to find the right code.Read
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