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59-42-7

中文名稱(chēng) 去氧腎上腺素堿
英文名稱(chēng) Phenylephrine
CAS 59-42-7
EINECS 編號(hào) 200-424-8
分子式 C9H13NO2
MDL 編號(hào) MFCD00044749
分子量 167.21
MOL 文件 59-42-7.mol
更新日期 2026/07/07 17:08:35
59-42-7 結(jié)構(gòu)式 59-42-7 結(jié)構(gòu)式

基本信息

中文別名
3-羥基-alpha-((甲基氨基)甲基)-芐醇
去氧腎上腺素堿
去羥腎上腺素
去氧腎上腺
新交感酚
新辛內(nèi)井林
英文別名
3-(1-HYDROXY-2-METHYLAMINO-ETHYL)PHENOL
L-PHENYLEPHRINE
(-)-PHENYLEPHRINE
PHENYLEPHRINE BASE
(-)-m-Hydroxy-alpha-(methylaminomethyl)benzyl alcohol
(-)-m-hydroxy-alpha-(methylaminomethyl)benzylalcohol
(-)-m-oxedrine
(R)-3-Hydroxy-alpha-[(methylamino)methyl]benzenemethanol hydrochloride
(r)-benzenemethano
(r)-phenylephrine
Adrianol
Ak-dilate
Ak-nefrin
Alcon efrin
Benzyl alcohol, m-hydroxy-alpha-((methylamino)methyl)-, (-)-
Biomydrin
component of Cerose dm
component of Comhist
component of Cyclomydril
component of Decongestant
所屬類(lèi)別
分析化學(xué):藥典標(biāo)準(zhǔn)品和雜質(zhì)標(biāo)準(zhǔn)品

物理化學(xué)性質(zhì)

熔點(diǎn)171°C
沸點(diǎn)295.79°C (rough estimate)
密度1.1222 (rough estimate)
折射率-55.5 ° (C=5, 1mol/L HCl)
儲(chǔ)存條件-20°C Freezer, Under inert atmosphere
溶解度Slightly soluble in water, sparingly soluble in methanol, slightly soluble in ethanol (96 per cent). It dissolves in dilute mineral acids and in dilute solutions of alkali hydroxides.
酸度系數(shù)(pKa)pKa 8.9 (Uncertain)
形態(tài)neat
顏色白色至灰白色
主要應(yīng)用pharmaceutical (small molecule)
InChIInChI=1/C9H13NO2/c1-10-6-9(12)7-3-2-4-8(11)5-7/h2-5,9-12H,6H2,1H3/t9-/s3
InChIKeySONNWYBIRXJNDC-DJEYLCQNNA-N
SMILES[C@H](C1C=CC=C(O)C=1)(O)CNC |&1:0,r|
CAS 數(shù)據(jù)庫(kù)59-42-7(CAS DataBase Reference)

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)腐蝕 (GHS05)有害 (GHS07)
GHS05,GHS07
警示詞危險(xiǎn)
危險(xiǎn)性描述H302-H315-H318-H335
危險(xiǎn)品標(biāo)志Xn
危險(xiǎn)類(lèi)別碼R22-R36/37/38
安全說(shuō)明S26-S36-S45
WGK GermanyWGK 3
RTECS號(hào)DO7175000
REACH 注冊(cè)登記Active
海關(guān)編碼2922.19.7000
存儲(chǔ)類(lèi)別11 - Combustible Solids
危險(xiǎn)性類(lèi)別Acute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
毒害物質(zhì)數(shù)據(jù)59-42-7(Hazardous Substances Data)
毒性LD50 oral in rat: 350mg/kg

應(yīng)用領(lǐng)域

用途一
擬腎上腺素藥物,用于外科手術(shù)延長(zhǎng)局部麻醉時(shí)間、鼻粘膜充血、急性低血壓、感染中毒性及過(guò)敏性休克等癥

知名試劑公司產(chǎn)品信息

去氧腎上腺素堿價(jià)格(試劑級(jí))
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱(chēng)CAS號(hào)包裝價(jià)格
2026/06/06P0395L-苯腎上腺素
L-Phenylephrine
59-42-75G170元
2026/06/06P0395L-苯腎上腺素
L-Phenylephrine
59-42-725G330元
2026/06/05HY-B0769R去氧腎上腺素堿
Phenylephrine (Standard)
59-42-710 mg370元

常見(jiàn)問(wèn)題列表

生物活性
(R)-(-)-Phenylephrine是選擇性的α1-腎上腺素受體激動(dòng)劑,主要用作減充血?jiǎng)?/span>
體外研究

(R)-(-)-Phenylephrine is a selective α 1 -adrenoceptor agonist with pK i values of 5.86, 4.87 and 4.70 for α 1D , α 1B and α 1A receptors respectively. Phenylephrine promotes cardiac fibroblast proliferation. Phenylephrine activates CaN and evokes NFAT3 nuclear translocation. It suggests that the Ca( 2+ )/CaN/NFAT pathway mediates phenylephrine -induced cardiac fibroblast proliferation, and this pathway might be a possible therapeutic target in cardiac fibrosis.

體內(nèi)研究

Perfusion of hearts with 100 μM phenylephrine causes a rapid (maximal at 10 min) 12-fold activation of two p38-MAPK isoforms. α 1 -adrenoceptor agonists such as phenylephrine increase the contractility of the heart. Phenylephrine also activates SAPKs/JNKs in neonatal ventricular myocytes. Phenylephrine could increase the alveolar fluid clearance in high tidal volume-ventilated rats and accelerate the absorption of pulmonary edema.

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