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Merck
CN

STS0213

Sigma-Aldrich

Brij® O10

greener alternative

别名:

Brij 97, C18-1E10, 聚氧乙烯(10)油醚

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关于此项目

线性分子式:
C18H35(OCH2CH2)nOH, n~10
CAS Number:
MDL编号:
UNSPSC代码:
12165104
NACRES:
NA.28
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描述

non-ionic

质量水平

表单

semisolid

分子量

~709 g/mol

环保替代产品特性

Use of Renewable Feedstocks
Design for Degradation
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

杂质

≤3.0% water

mp

25 °F

酸值

≤1.0 mg KOH/g

羟基值

75‑95 mg KOH/g

溶解性

water: 100 mg/mL, clear, colorless to faintly yellow

密度

1 g/mL at 25 °C (lit.)

HLB

12.4

环保替代产品分类

SMILES字符串

O(CCO)CCCCCCCC\C=C/CCCCCCCC

InChI

1S/C20H40O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19-22-20-18-21/h9-10,21H,2-8,11-20H2,1H3/b10-9-

InChI key

KWVPFECTOKLOBL-KTKRTIGZSA-N

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一般描述

ECO Brij® O10, also known as oleyl alcohol polyoxyethylene ether, is a bio-based, high HLB nonionic surfactant manufactured from naturally occurring straight-chain oleyl alcohol. This detergent, derived from natural sources, provides various functional advantages, such as detergency, emulsification, and wetting, making it suitable for a range of applications in biochemical and biological research.
The ECO Brij series of ethoxylated fatty alcohols are non-ionic surfactants manufactured using renewable sources. ECO Brij O10 is a mixture of decaethylene glycol alkenyl ethers, primarily oleyl (C18:1) ether. The fatty alcohol ether profile of ECO Brij O10 may differ lot-to-lot due to natural variability in the lipid starting material (palm oil).
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Green Chemistry. This product is a biobased surfactant and is aligned with the 7th principle of Green Chemistry "Use of Renewable Feedstocks" and the 10th principle "Design for Degradation".

应用

Brij® O10 has been used in a study to assess the aqueous surfactant two-phase systems for the continuous countercurrent cloud point extraction.

特点和优势

  • 100 % Renewable
  • 100 % Bio-based
  • Certified to the USDA BioPreferred Program
  • Lower carbon footprint than petrochemical-based versions
  • High-purity chemical suitable for a wide variety of research applications

其他说明

For additional information on our range of Biochemicals, please complete this form.

法律信息

Brij is a registered trademark of Croda International PLC
ECO BRIJ is a registered trademark of Croda Inc.

象形图

Exclamation markEnvironment

警示用语:

Warning

危险声明

危险分类

Aquatic Chronic 2 - Skin Irrit. 2

储存分类代码

11 - Combustible Solids

WGK

WGK 1

闪点(°F)

>464.0 °F - Equilibrium method

闪点(°C)

> 240 °C - Equilibrium method


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Aqueous Surfactant Two-Phase Systems for the Continuous Countercurrent Cloud Point Extraction
Ingram, T., et al.
Chemie Ingenieur Technik, 84, 840-840 (2012)
Yash Kapoor et al.
International journal of pharmaceutics, 361(1-2), 222-229 (2008-06-26)
Cyclosporine A (CyA) is an immunosuppressant drug that is used for treating a variety of ocular diseases and disorders. CyA is commonly delivered via eye drops, which is highly inefficient due to a low bioavailability of less than 5%. The
Myriam Chentouf et al.
Journal of immunology (Baltimore, Md. : 1950), 179(1), 409-420 (2007-06-21)
The biological effects of rIgG(1) 13B8.2, directed against the CDR3-like loop on the D1 domain of CD4, are partly due to signals that prevent NF-kappaB nuclear translocation, but the precise mechanisms of action, particularly at the level of membrane proximal
R B Shah et al.
International journal of pharmaceutics, 341(1-2), 189-194 (2007-05-25)
In the present work, a novel application of ultrasonic measurements is detailed to characterize nano-emulsion formulations as a part of the overall Quality by Design (QbD) goal. Ultrasonic resonator technology (URT) was utilized to measure sound velocity and absorption of
Doaa Ahmed El-Setouhy et al.
The Journal of pharmacy and pharmacology, 62(1), 25-34 (2010-08-21)
The objective of this study was to improve systemic delivery of the highly analgesic ketorolac trometamol (ketorolac tromethamine) via the transdermal route, through cost-effective topical formulations, to avoid most of the problems associated with ketorolac trometamol therapy. In-vitro release behaviour

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