アンブロキソール塩酸塩(18683-91-5)

ChemicalBook Optimization Suppliers
名前: JinYan Chemicals(ShangHai) Co.,Ltd.  
電話番号: 13817811078
電子メール: sales@jingyan-chemical.com
名前: Adamas Reagent, Ltd.  
電話番号: 400-6009262 16621234537
電子メール: zhangsn@titansci.com
名前: LGM Pharma  
電話番号: 1-(800)-881-8210
電子メール: inquiries@lgmpharma.com
名前: Nanjing Chemlin Chemical Co., Ltd  
電話番号: 025-83697070
電子メール: info@chemlin.com.cn
名前: China Langchem Inc.  
電話番号: 0086-21-58956006
電子メール:
アンブロキソール塩酸塩 製品概要
化学名:アンブロキソール塩酸塩
英語化学名:Ambroxol
别名:4-((2-amino-3,5-dibromobenzyl)amino)-(e)-cyclohexano;5-dibromophenyl)methyl)amino)-4-(((2-amino-trans-cyclohexano;Cyclohexanol, 4-((2-amino-3,5-dibromobenzyl)amino)- (E)-;Cyclohexanol, 4-[[(2-amino-3,5-dibromophenyl)methyl]amino]-, trans-;n-(2-amino-3,4-dibromociclohexil)-trans-4-aminociclohexanol;n-(2-amino-3,4-dibromocyclohexyl)-trans-4-aminocyclohexanol;N-(trans-4-Hidroxiciclohexil)-(2-amino-3,5-dibromobencil)amina;N-(trans-4-Hydroxycyclohexyl)-(2-amino-3,5-dibromobenzyl)-amine
CAS番号:18683-91-5
分子式:C13H18Br2N2O
分子量:378.1
EINECS:242-500-3
カテゴリ情報:API
Mol File:18683-91-5.mol
アンブロキソール塩酸塩
アンブロキソール塩酸塩 物理性質
融点 233-234 C
沸点 468.6±45.0 °C(Predicted)
比重(密度) 1.5863 (rough estimate)
屈折率 1.6220 (estimate)
貯蔵温度 Keep in dark place,Sealed in dry,2-8°C
溶解性Soluble in Water.
外見 solid
酸解離定数(Pka)15.12±0.40(Predicted)
White
安定性:Stable for 1 year from date of purchase as supplied. Solutions in distilled water may be stored at -20° for up to 3 months.
CAS データベース18683-91-5(CAS DataBase Reference)
NISTの化学物質情報Ambroxol(18683-91-5)
安全性情報
主な危険性 Xn,Xi
Rフレーズ 22-36/37/38
Sフレーズ 36-26
WGK Germany 3
RTECS 番号GV8423000
毒性guinea pig,LD50,intraperitoneal,280mg/kg (280mg/kg),Medicamentos de Actualidad. Vol. 15, Pg. 523, 1979.
MSDS Information
アンブロキソール塩酸塩 Usage And Synthesis
用途アンブロキソール(英語?ドイツ語: Ambroxol)は、去痰薬に属する医薬品の1種であり、痰の喀出に困難を伴う急性および慢性の下部気道症状の治療、および急性の咽頭部痛を緩和するのに用いられる。
用途肺胞表面活性代謝物の分泌を 増加します。
効能去痰薬, 粘液溶解薬
説明Ambroxol HCl (18683-91-5) is a radical scavenger with anti-inflammatory activity. Blocks the generation of reactive oxygen species by bronchoalveolar lavage cells, inhibits doxorubicin-induced lipid peroxidation (70 mg/kg in rat), and inhibits the release of inflammatory mediators from human leukocytes and mast cells (effective dose ~ 100 μM)
OriginatorMucosolvan,Thomae,W. Germany,1980
使用Ambroxol is a metabolite of Bromohexine. Ambroxol Hydrochloride is a bronchosecretolytic drug. Free base of Ambroxol Hydrochloride (A575900).
使用expectorant
定義ChEBI: Ambroxol is an aromatic amine.
Manufacturing Process6.5 g of N-(trans-p-hydroxycyclohexyl)-(2-aminobenzyl)-amine were dissolved in a mixture of 80 cc of glacial acetic acid and 20 cc of water, and then 9.6 g of bromine were added dropwise at room temperature while stirring the solution. After all of the bromine had been added, the reaction mixture was stirred for two hours more and was then concentrated in a water aspirator vacuum. The residue was taken up in 2 N ammonia, the solution was extracted several times with chloroform, and the organic extract solutions were combined and evaporated. The residue, raw N-(trans-phydroxycyclohexyl)-( 2-amino-3,5-dibromobenzyl)-amine, was purified with chloroform and ethyl acetate over silica gel in a chromatographic column, the purified product was dissolved in a mixture of ethanol and ether, and the solution was acidified with concentrated hydrochloric acid. The precipitate formed thereby was collected and recrystallized from ethanol and ether, yielding N-(trans-p-hydroxycyclohexyl)-(2-amino-3,5-dibromobenzyl)-amine hydrochloride, MP 233-234.5°C (decomposition).
Therapeutic FunctionExpectorant
参考文献1) Teramoto et al. (1999), Effects of ambroxol on spontaneous or stimulated generation of reactive oxygen species by bronchoalveolar lavage cells harvested from patients with or without chronic obstructive pulmonary diseases; Pharmacology, 59 135 2) Nowak et al. (1995), Ambroxol inhibits doxorubicin-induced lipid peroxidation in heart of mice; Free Radic. Biol. Med., 19 659 3) Gibbs et al. (1999), Ambroxol inhibits the release of histamine, leukotrienes and cytokines from human leukocytes and mast cells; Inflamm. Res., 48 86
Tags:18683-91-5