HOMATROPINE

Base Information Edit

Chemical Name:HOMATROPINE
CAS No.:87-00-3
Deprecated CAS:16175-83-0,104441-60-3,104441-60-3
Molecular Formula:C16H21 N O3
Molecular Weight:275.348
Hs Code.:2933990090
European Community (EC) Number:201-716-8
UNII:8QS6WCL55Z
DSSTox Substance ID:DTXSID6044014,DTXSID00858826
Nikkaji Number:J253.896B
Wikipedia:Homatropine
Wikidata:Q1038115,Q106039245
NCI Thesaurus Code:C61783
RXCUI:27084
ChEMBL ID:CHEMBL1618018
Mol file:87-00-3.mol

Synonyms:1aH,5aH-Tropan-3a-ol, (?à)-mandelate (ester) (8CI);Benzeneacetic acid, a-hydroxy-, 8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester, endo-(?à)-; (?à)-Homatropine; (?à)-Mandelic acid 1aH,5aH-tropan-3a-ylester; (?à)-Mandelyltropine; Benzeneaceticacid, a-hydroxy-,8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester, endo-; Homatropin; Homatropine; Homoatropine;Mandelyltropeine; Tropine (?à)-mandelate (ester); Tropine mandelate

Suppliers and Price of HOMATROPINE

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
HOMATROPINE 95.00%
10MG
$ 705.82

AHH
Homatropine 98%
50g
$ 230.00

Total 26 raw suppliers

Chemical Property of HOMATROPINE Edit

Chemical Property:

Melting Point:100ºC
Refractive Index:1.5500 (estimate)
Boiling Point:403.3 ºC
PKA:pKa 9.9 (Uncertain)
Flash Point:197.7 ºC
PSA：49.77000
Density:1.21 g/cm³
LogP:1.82630
XLogP3:1.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:4
Exact Mass:275.15214353
Heavy Atom Count:20
Complexity:340

Purity/Quality:

99%min ^*data from raw suppliers

HOMATROPINE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s): Moderately toxic by ingestion and subcutaneous routes.
Hazard Codes:Moderately toxic by ingestion and subcutaneous routes.

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C2CCC1CC(C2)OC(=O)C(C3=CC=CC=C3)O
Isomeric SMILES:CN1[C@@H]2CC[C@H]1CC(C2)OC(=O)C(C3=CC=CC=C3)O
Uses Anticholinergic (ophthalmic).

Technology Process of HOMATROPINE

There total 1 articles about HOMATROPINE which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: