
CAS Number87-00-3
SynonymsOmatropina [DCIT]; Homatropin; Homotropine; DL-mandelic acid-tropane-3endo-yl ester; Homoatropine; homatropine; Mandelyltropeine; Homatropine [BAN]; Methylhomatropinum; DL-Mandelsaeure-tropan-3endo-ylester; EINECS 201-716-8; homatropine hydrobromide; 8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester; Mandelytropeine; MFCD00067305
Molecular FormulaC16H21NO3
Molecular Weight311.80
Purity98%
Density1.21 g/cm3
Boiling Point403.3ºC
Melting Point100ºC
| Chemical & Physical Properties | |
|---|---|
| CAS Number | 87-00-3 |
| Catalog No. | 2A-9010853 |
| Chinese Name | 后马托品 |
| Synonyms | Omatropina [DCIT]; Homatropin; Homotropine; DL-mandelic acid-tropane-3endo-yl ester; Homoatropine; homatropine; Mandelyltropeine; Homatropine [BAN]; Methylhomatropinum; DL-Mandelsaeure-tropan-3endo-ylester; EINECS 201-716-8; homatropine hydrobromide; 8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester; Mandelytropeine; MFCD00067305 |
| Molecular Formula | C16H21NO3 |
| Molecular Weight | 311.80 |
| Purity | 98 |
| Density | 1.21 g/cm3 |
| Boiling Point | 403.3ºC |
| Melting Point | 100ºC |
| Application | Homatropine is an orally active muscarinic acetylcholine receptor antagonist that can be used as an anticholinergic drug [1]. |
| HTC | 2933990090 |
| MDL Number | MFCD00050613 |
| SMILES | Cl.N1([C@@H]2C[C@H](C[C@H]1CC2)OC(=O)C(O)c3ccccc3)C |
| InChI | InChI=1S/C4H3ClF4O2/c1-11-2(10)3(6,7)4(5,8)9/h1H3 |
| InChI Key | FRMDDIJBLQNNTC-RDYJJYPNSA-N |
| NACRES Code | NA.21 |
| UNSPSC | 12352200 |
| MSDS | msds/10853_1_87_00_3.pdf |
| Use of | Homatropine is an orally active muscarinic acetylcholine receptor antagonist and can be used as an anticholinergic agent[1]. Properties Name [(1R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 2-hydroxy-2-phenylacetate Synonym More Synonyms Homatropine Biological Activity Description Homatropine is an orally active muscarinic acetylcholine receptor antagonist and can be used as an anticholinergic agent[1]. Related Catalog Signaling Pathways >> Neuronal Signaling >> mAChR Signaling Pathways >> GPCR/G Protein >> mAChR Research Areas >> Neurological Disease In Vitro Homatropine (20 μM) alone produces a dose ratio of 259 in atrium from guinea-pigs, and produces a dose ratio of only 95.0 when combined with Hexamethonium Bromide (HY-B0569) in atrium from guinea-pigs[1]. Homatropine has affinities for muscarinic receptors in stomach (pA2 = 7.13) and for those in atria mediating force (pA2 = 7.21) and rate (pA2 = 7.07) responses[2]. Chemical & Physical Properties Molecular Formula C16H21NO3 Exact Mass 275.15200 PSA 49.77000 LogP 1.82630 InChIKey ZTVIKZXZYLEVOL-DGKWVBSXSA-N Toxicological Information CHEMICAL IDENTIFICATION RTECS NUMBER : CHEMICAL NAME : 1-alpha-H,5-alpha-H-Tropan-3-alpha-ol, mandelate (ester) CAS REGISTRY NUMBER : BEILSTEIN REFERENCE NO. : LAST UPDATED : DATA ITEMS CITED : MOLECULAR FORMULA : C16-H21-N-O3 MOLECULAR WEIGHT : WISWESSER LINE NOTATION : T56 A ANTJ A1 GOVYQR HEALTH HAZARD DATA ACUTE TOXICITY DATA TYPE OF TEST : LDLo - Lowest published lethal dose ROUTE OF EXPOSURE : Intraperitoneal SPECIES OBSERVED : Rodent - rat DOSE/DURATION : TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : TXAPA9 Toxicology and Applied Pharmacology. (Academic Press, Inc., 1 E. First St., Duluth, MN 55802) V.1- 1959- Volume(issue)/page/year: 1,156,1959 TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : SPECIES OBSERVED : Rodent - mouse DOSE/DURATION : TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : FRXXBL French Demande Patent Document. (U.S. Patent and Trademark Office, Foreign Patents, Washington, DC 20231) Volume(issue)/page/year: #2035763 TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : Intraperitoneal SPECIES OBSERVED : Rodent - mouse DOSE/DURATION : TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : FRXXBL French Demande Patent Document. (U.S. Patent and Trademark Office, Foreign Patents, Washington, DC 20231) Volume(issue)/page/year: #2035763 TYPE OF TEST : LD50 - Lethal dose, 50 percent kill ROUTE OF EXPOSURE : Subcutaneous SPECIES OBSERVED : Rodent - mouse DOSE/DURATION : TOXIC EFFECTS : Details of toxic effects not reported other than lethal dose value REFERENCE : FRXXBL French Demande Patent Document. (U.S. Patent and Trademark Office, Foreign Patents, Washington, DC 20231) Volume(issue)/page/year: #2035763 *** NIOSH STANDARDS DEVELOPMENT AND SURVEILLANCE DATA *** NIOSH OCCUPATIONAL EXPOSURE SURVEY DATA : NOHS - National Occupational Hazard Survey (1974) NOHS Hazard Code - 84350 No. of Facilities: 170 (estimated) No. of Industries: 1 No. of Occupations: 6 No. of Employees: 2582 (estimated) Safety Information HS Code 2933990090 Synthetic Route Total: 1 Page Mandelic acid CAS#:611-71-2 CAS#:120-29-6 Homatropine CAS#:87-00-3 Literature: Journal fuer Praktische Chemie (Leipzig), , vol. <2> 117, p. 147 |
| Tax Rebate | 13.0% |
| Supervision | None. MFN tariff: 6.5%. Ordinary tariff: 20.0% |
| Transport Info | Product name: Chinese name Houmatropin English name [(1R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 2-hydroxy-2-phenylacetate Chinese alias mandelyltropine | 8-methyl-8-azabicyclo[3.2.1]octane-3-ol hydroxy(phenyl)acetate English aliases more |
| Related Products in Specialty Chemicals | ||
|---|---|---|
| Hexestrol | 84-16-2 | 2A-9010848 |
| Hexobendine | 54-03-5 | 2A-9010849 |
| Hinokitiol | 499-44-5 | 2A-9010850 |
| Hirsutine | 7729-23-9 | 2A-9010851 |
| Histrelin | 76712-82-8 | 2A-9010852 |
| Homatropine hydrobromide | 51-56-9 | 2A-9010854 |
| Homatropine methyl bromide | 80-49-9 | 2A-9010855 |
| Homoeriodictyol | 107657-60-3 | 2A-9010856 |
| Homprenorphine | 16549-56-7 | 2A-9010858 |
| Honeysuckle absolute | 8023-93-6 | 2A-9010859 |
| Browse all Specialty Chemicals products » | ||
Phone:
630-322-8886
630-322-8887
Email:
Office Locations:
Chicago, IL, USA
San Francisco, CA, USA