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3-苯丙醇

规格或纯度: 99%
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货号 (SKU) 包装规格 是否现货 价格 数量
P103663-25ml
25ml 现货 Stock Image
P103663-100ml
100ml 现货 Stock Image
P103663-500ml
500ml 现货 Stock Image
P103663-1L
1L 现货 Stock Image
P103663-5L
5L 现货 Stock Image
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非杂环砌块

基本描述

别名 γ-苯丙醇|氢化肉桂醇|3-苯基-1-丙醇|苯丙醇|利胆醇
英文别名 3-PHENYL-1-PROPANOL|3-Phenylpropan-1-ol|122-97-4|Benzenepropanol|Hydrocinnamyl alcohol|3-Phenylpropanol|3-Phenylpropyl alcohol|Hydrocinnamic alcohol|3-Benzenepropanol|Phenylpropyl alcohol|1-Propanol, 3-phenyl-|3-Phenyl-n-propanol|(3-Hydroxypropyl)benzene|
规格或纯度 99%
英文名称 3-phenylpropanol
应用 用于合成香料和医药品。在医药工业中是中枢骨骼肌松弛剂强筋松的中间体。 作为化妆品中防腐剂,3-苯丙醇带有对细菌和霉菌抗菌性能的自然香味。因此用在与胡椒醛或胡椒的组合作为化妆品的防腐剂。 3-苯丙醇或其酯衍生物被用作鲜花的香味成分,如丁香花,风信子,以及由于其具有香醋气味特征也作为铃兰的组成部分。
运输条件 常规运输
产品介绍

有果香。微溶于水,溶解度: 10.3 g/l 水(20°C) ,溶于甲醇、苯、环己烷和乙酸乙酯。

Product Introduction

3-Phenyl-1-propanol is a fragrance ingredient.


Application

3-Phenyl-1-propanol was used to study the hydrogenation of trans-cinnamaldehyde using water-soluble organometallic complexes. It was used as starting reagent during the enantioselective synthesis of (S)- and (R)-dapoxetine.

名称和标识符

PubChem SID 488183140
EC号 204-587-6
IUPAC Name 3-phenylpropan-1-ol
INCHI InChI=1S/C9H12O/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6,10H,4,7-8H2
InChi Key VAJVDSVGBWFCLW-UHFFFAOYSA-N
Canonical SMILES C1=CC=C(C=C1)CCCO
Isomeric SMILES C1=CC=C(C=C1)CCCO
WGK Germany 1
RTECS UB8970000
PubChem CID 31234
分子量 136.19
Beilstein号 1857542
Reaxy-Rn 1857542

化学和物理性质

溶解性 Not miscible in water.
密度 1
折光率 1.5365
闪点(℉) 248 °F
闪点(℃) 120℃
沸点 119-121°C
熔点 -18°C

安全和危险性(GHS)

象形图
ghs07

Harmful

信号词 Warning
危险声明 H315: Causes skin irritation
H319: Causes serious eye irritation
预防措施声明 P305+P351+P338,P280,P302+P352,P321,P264,P362+P364,P264+P265,P337+P317,P332+P317
WGK Germany 1
RTECS UB8970000
Reaxy-Rn 1857542
个人防护装备 Eyeshields,full-face respirator (US),Gloves,multi-purpose combination respirator cartridge (US),type ABEK (EN14387) respirator filter

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参考文献

1. Jörgen Samuelsson,Torgny Undin,Anders Törncrona,Torgny Fornstedt.  (2010-10-12)  Improvement in the generation of adsorption isotherm data in the elution by characteristic points method--the ECP-slope approach..  Journal of chromatography. A,  1217  ((46)):  (7215-7221).  [PMID:20933238]
2. D Belsito,D Bickers,M Bruze,P Calow,M Dagli,A D Fryer,H Greim,Y Miyachi,J H Saurat,I G Sipes.  (2011-08-09)  A toxicologic and dermatologic assessment of cinnamyl phenylpropyl materials when used as fragrance ingredients..  Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association,  49 Suppl 2  ():  (S256-S267).  [PMID:21820026]
3. S P Bhatia,G A Wellington,J Cocchiara,J Lalko,C S Letizia,A M Api.  (2011-08-23)  Fragrance material review on 3-phenyl-1-propanol..  Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association,  49 Suppl 2  ():  (S246-S251).  [PMID:21855595]
4. Ritwika Ray,Rahul Dev Jana,Mayukh Bhadra,Debabrata Maiti,Goutam Kumar Lahiri.  (2014-10-07)  Efficient and simple approaches towards direct oxidative esterification of alcohols..  Chemistry (Weinheim an der Bergstrasse, Germany),  20  ((47)):  (15618-15624).  [PMID:25284591]
5. E Baciocchi,M Fabbrini,O Lanzalunga,L Manduchi,G Pochetti.  (2001-02-13)  Prochiral selectivity in H(2)O(2)-promoted oxidation of arylalkanols catalysed by chloroperoxidase. The role of the interactions between the OH group and the amino-acid residues in the enzyme active site..  European journal of biochemistry,  268  ((3)):  (665-672).  [PMID:11168405]
6. Soyeong Kang,Hyeon-Kyu Lee.  (2009-12-05)  Highly efficient, enantioselective syntheses of (S)-(+)- and (R)-(-)-dapoxetine starting with 3-phenyl-1-propanol..  The Journal of organic chemistry,  75  ((1)):  (237-240).  [PMID:19957926]
7. Ryan L Jones,Bronwyn L Harrod,James D Batteas.  (2010-09-23)  Intercalation of 3-phenyl-1-proponal into OTS SAMs on silica nanoasperities to create self-repairing interfaces for MEMS lubrication..  Langmuir : the ACS journal of surfaces and colloids,  26  ((21)):  (16355-16361).  [PMID:20857994]