基本情報
- CAS
329-63-5- 標準SMILES
CNCC(O)c1ccc(O)c(O)c1.Cl- InChIKey
ATADHKWKHYVBTJ-UHFFFAOYSA-N- 分子式
- C9H14ClNO3
- 平均分子量
- 219.66 g/mol
- 単同位体質量
- 219.06622099
概要
Racepinephrine Hydrochloride is an organic molecular entity.
名称と識別子
- 優先名称
- (+-)-Epinephrine hydrochloride
- IUPAC
- 4-[1-hydroxy-2-(methylamino)ethyl]benzene-1,2-diol;hydrochloride
- 現地名
- DL-アドレナリン塩酸塩
- 英語名
- DL-Adrenaline hydrochloride
- 分子式
- C9H14ClNO3
- 分子量
- 219.67
名称と別名
329-63-5Racepinephrine hydrochlorideAsthmanefrin(+-)-Epinephrine hydrochlorideRacepinephrine HClRacepinefrine hydrochlorideAdrenaline hydrochloride, dl-Epinephrine hydrochloride, dl-336096P2WE1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]-, hydrochlorideEPINEPHRINE DL-FORM HYDROCHLORIDEEPINEPHRINE,RACEMIC HYDROCHLORIDE
名称をさらに表示
DL-アドレナリン塩酸塩(±)-エピレナミン塩酸塩DL-エピネフリン塩酸塩rac-(R*)-α-[(メチルアミノ)メチル]-3,4-ジヒドロキシベンジルアルコール·塩酸塩(±)-アドレナリン·塩酸塩(±)-エピネフリン·塩酸塩(±)‐エピネフリン塩酸塩標準品(±)-エピネフリン 塩酸塩(±)-エピネフリン塩酸塩標準品RAC EPINEPHRINE HCLDL-EPINEPHRINE HYDROCHLORIDEDL-EpinephAdrenalin HCLAdrenaline HCLEpinephrin HClDL-adrenaline hclrs-epinephrine hclTIMTEC-BB SBB003360Racepinephrine HydrochL
1,2-Benzenediol, 4-(1-hydroxy-2-(methylamino)ethyl)-, hydrochlorideEpi-MistS2 RacepinephrineRefChem:55960S2 Racepinephrine MULTI-DOSE206-346-0DL-ADRENALINE HYDROCHLORIDE(+/-)-Epinephrine hydrochloride
物性
構造計算による物性
- 極性表面積
- 72.7 Ų
- 水素結合供与体数
- 5
- 水素結合受容体数
- 4
- 回転可能結合数
- 3
- 重原子数
- 14
- 形式電荷
- 0
- 複雑度
- 154
物理化学的性質
- 融点
- 157 ° · 157°
- 貯蔵温度
- 2 · 2-8°C
- 溶解性
- 2 O: · H2O: >50 mg/mL
- 外見
- A crystalline solid
- 水溶解度
- 2 O: · H2O: 50mg/mL
- Merck
- 14 · 14,3619
- 安定性
- 安定していますが、光に敏感です。酸、酸塩化物、酸無水物、酸化剤とは混和しません。
- InChI
- InChI=1S/C9H13NO3.ClH/c1-10-5-9(13)6-2-3-7(11)8(12)4-6;/h2-4,9-13H,5H2,1H3;1H
- InChIKey
- ATADHKWKHYVBTJ-UHFFFAOYSA-N
- SMILES
- C1(C(O)CNC)=CC=C(O)C(O)=C1.Cl
- CAS データベース
- 329 · 329-63-5(CAS DataBase Reference)
- EPAの化学物質情報
- (+-)-Epinephrine hydrochloride (329-63-5)
化学的性質
化学的特性solid
安全と法規制
安全情報は参考情報です。供給元の安全データシート（SDS）、適用法令、専門家による評価に代わるものではありません。
GHS分類
GHS Classification
Danger
H301 (97.6%): Toxic if swallowed [Danger Acute toxicity, oral]
P261, P262, P264, P264+P265, P270, P271, P280, P301+P316, P302+P352, P304+P340, P305+P351+P338, P316, P319, P321, P330, P332+P317, P337+P317, P361+P364, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 41 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
危険有害性情報
Regulatory Information1,2-Benzenediol, 4-1-hydroxy-2-(methylamino)ethyl-, hydrochloride: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.
Hazard Classes and CategoriesAcute Tox. 3 (97.6%)
安全データ
- wgk
- 3
- tsca
- TSCA listed
- rtecs
- DO3330000
- ridadr
- UN 2811 6.1/PG 2
- hs_code
- 2937901500
- risk_code
- 24/25-36/37/38
- hazard_code
- T
- safety_code
- 26-36/37-45
- hazard_class
- 6.1(a)
- packing_group
- II
- Hazard Classifications
- Acute Tox. 3 DermalAcute Tox. 3 InhalationAcute Tox. 3 OralFlam. Liq. 2STOT SE 1
- ストレージクラス
- 3 - Flammable liquids
化学と産業
薬理情報
MeSH Pharmacological Classification
Drugs that selectively bind to and activate alpha adrenergic receptors.
Drugs that selectively bind to and activate beta-adrenergic receptors.
Agents that cause an increase in the expansion of a bronchus or bronchial tubes.
Agents that dilate the pupil. They may be either sympathomimetics or parasympatholytics.
Drugs that mimic the effects of stimulating postganglionic adrenergic sympathetic nerves. Included here are drugs that directly stimulate adrenergic receptors and drugs that act indirectly by provoking the release of adrenergic transmitters.
Drugs used to cause constriction of the blood vessels.
用途と製造
General Manufacturing Information1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]-, hydrochloride (1:1): ACTIVE
応用分野
使用bronchodilatator,
一般的な説明Epinephrine (adrenalin) is synthesized from norepinephrine (noradrenalin) by the action of the enzyme phenylethanolamine N-methyltransferase. Epinephrine comprises 5%-10% of the total catecholamines in the central nervous system. It is a mixed α/β-adrenergic receptor agonist and stimulates these receptors. Their site of synthesis is adrenal medulla and it travels through the vascular systems. Its breakdown occurs in the central nervous system (CNS), liver and kidney.
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