Pro_Molecular_Structure:
pro_cdbregno:CCD00011810
盐酸邻甲苯海拉明
pro_cas:
341-69-5
pro_formula:C18 H23 N O . Cl H
pro_molWeight:305.847
* If the product has intellectual property rights, a license granted is must or contact us.
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| Product_Name： | 盐酸邻甲苯海拉明 |
| CAS： | 341-69-5 |
| 中文同义词： | 盐酸邻甲苯海拉明 |
| EnglishSynonyms： | N,N-DIMETHYL-2-(2-METHYLBENZHYDRYLOXY)ETHYLAMINE HYDROCHLORIDE ; O-METHYLDIPHENHYDRAMINE HYDROCHLORIDE ; DIMETHYL((2-[(2-METHYLPHENYL)(PHENYL)METHOXY]ETHYL))AMINE HYDROCHLORIDE ; BETA-DIMETHYLAMINOETHYL 2-METHYLBENZHYDRYL ETHER HYDROCHLORIDE ; ORPHENADRINE HYDROCHLORIDE |
| pro_mdlNumber： | MFCD00012480 |
| pro_acceptors： | 2 |
| pro_donors： | 0 |
| pro_smile： | Cc1ccccc1C(c2ccccc2)OCCN(C)C.Cl |
| InChi： | InChI=1S/C18H23NO.ClH/c1-15-9-7-8-12-17(15)18(20-14-13-19(2)3)16-10-5-4-6-11-16;/h4-12,18H,13-14H2,1-3H3;1H |
| InChiKey： | InChIKey=UQZKYYIKWZOKKD-UHFFFAOYSA-N |
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| MeltingPoint： | 160-164 DEG C |
| Comments： | BIOCHEM/PHYSIOL ACTIONS: H1 HISTAMINE RECEPTOR ANTAGONIST BIOCHEM/PHYSIOL ACTIONS: MUSCARINIC RECEPTOR ANTAGONIST BIOCHEM/PHYSIOL ACTIONS: MUSCLE RELAXANT. ORPHENADRINE HAS ALSO BEEN REPORTED TO INHIBIT THE NORADRENERGIC TRANSPORTER AND TO BLOCK THE NMDA RECEPTOR ION CHANNEL RIDADR: UN 2811 6.1/PG 3 RTECS: KR6300000 UNSPSC: 12352100 WGK: 3 |
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| secure_symbol： |
GHS06
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| secure_signal_word： | Danger |
| secure_risk_stmt： | H301 |
| secure_cautionary_stmt： | P301 + P310 |
| secure_damage_code： | Xn |
| secure_risk_disclosure_stmt： | R:22 |
| secure_security_stmt： | S:36 |
| secure_wgk_germany： | 3 |
basic_info
* If the product has intellectual property rights, a license granted is must or contact us.
