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主要文件

安全信息

175404

Sigma-Aldrich

4-异丙基苯酚

98%

别名:

对枯烯醇

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1 G
¥987.67

¥987.67


预计发货时间2025年6月20日详情


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1 G
¥987.67

About This Item

线性分子式:
(CH3)2CHC6H4OH
CAS号:
分子量:
136.19
Beilstein:
1363564
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

¥987.67


预计发货时间2025年6月20日详情


获取大包装报价

蒸汽密度

>1 (vs air)

方案

98%

表单

crystals

沸点

212-213 °C (lit.)

mp

59-61 °C (lit.)

SMILES字符串

CC(C)c1ccc(O)cc1

InChI

1S/C9H12O/c1-7(2)8-3-5-9(10)6-4-8/h3-7,10H,1-2H3

InChI key

YQUQWHNMBPIWGK-UHFFFAOYSA-N

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此商品
PHR1006S388985529
山梨醇 Pharmaceutical Secondary Standard; Certified Reference Material

PHR1006

山梨醇

D -山梨醇 ≥98% (GC), BioReagent, suitable for cell culture, suitable for plant cell culture

S3889

D -山梨醇

D -山梨醇 BioUltra, ≥99.0% (HPLC)

85529

D -山梨醇

form

viscous liquid

form

-

form

powder

form

powder

color

colorless

color

-

color

white

color

colorless

concentration

70 wt. % in H2O

concentration

-

concentration

-

concentration

-

refractive index

n20/D 1.46

refractive index

-

refractive index

-

refractive index

-

density

1.28 g/mL at 25 °C

density

-

density

-

density

-

一般描述

对 4-异丙基苯酚的声化学降解进行了研究 [1]

应用

乙烯基化合物的合成中使用了 4-异丙基苯酚 [2]

象形图

CorrosionExclamation mark

警示用语:

Danger

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

储存分类代码

8B - Non-combustible corrosive hazardous materials

WGK

WGK 3

闪点(°F)

230.0 °F - Pensky-Martens closed cup

闪点(°C)

110 °C - Pensky-Martens closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

法规信息

危险化学品

  • 历史批次信息供参考:

    分析证书(COA)

    Lot/Batch Number

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    Mahdi Chiha et al.
    Ultrasonics sonochemistry, 17(5), 773-782 (2010-04-15)
    Sonochemical degradation of phenol (Ph), 4-isopropylphenol (4-IPP) and Rhodamine B (RhB) in aqueous solutions was investigated for a large range of initial concentrations in order to analyze the reaction kinetics. The initial rates of substrate degradation and H(2)O(2) formation as
    Frédéric L P Gabriel et al.
    Chemistry & biodiversity, 4(9), 2123-2137 (2007-09-25)
    Sphingobium xenophagum Bayram is capable of metabolizing 4-alkoxyphenols and endocrine disruptive alpha-quaternary 4-nonylphenols by an ipso-substitution mechanism that involves ring hydroxylation at the site of the substituent. Here, we show that Bayram's ipso-hydroxylating activity was able to transform also bisphenol
    Ye Eun Park et al.
    Nutrients, 12(1) (2020-01-23)
    Probiotics can improve the intestinal environment by enhancing beneficial bacteria to potentially regulate lipid levels; however, the underlying mechanisms remain unclear. The aim of this study was to investigate the effect of Lactobacillus plantarum Q180 (LPQ180) on postprandial lipid metabolism
    David J Hopper et al.
    Applied and environmental microbiology, 69(6), 3650-3652 (2003-06-06)
    4-ethylphenol methylenehydroxylase from Pseudomonas putida JD1 acts by dehydrogenation of its substrate to give a quinone methide, which is then hydrated to an alcohol. It was shown to be active with a range of 4-alkylphenols as substrates. 4-n-propylphenol, 4-n-butylphenol, chavicol
    Shogo Kumagai et al.
    Scientific reports, 8(1), 13994-13994 (2018-09-20)
    The pyrolysis of bisphenol A (BPA), an essential process ingredient used in industry and many everyday life products, helps produce low-industrial-demand chemicals such as isopropenyl- and isopropyl-phenols (IPP and iPrP). In this study, tandem micro-reactor gas chromatography/mass spectrometry combined with

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