STS0214
BRIJ® O20
average Mn ~1,150
別名:
Brij® 98, ポリオキシエチレン(20)オレイルエーテル
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この商品について
化学式:
C18H35(OCH2CH2)nOH, n~20
CAS番号:
分子量:
1149.53
UNSPSC Code:
12165104
NACRES:
NA.28
MDL number:
SMILES string
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
description
non-ionic
form
solid
mol wt
average Mn ~1,150
greener alternative product characteristics
Use of Renewable Feedstocks
Design for Degradation
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
mp
25-30 °C (lit.)
hydroxyl value
50‑65 mg KOH/g
solubility
water: soluble 1 g/L at 20 °C
density
0.901 g/cm3 at 20 °C
HLB
15.5
greener alternative category
Quality Level
General description
ECO Brij® O20, 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.
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".
Features and Benefits
- 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
Other Notes
For additional information on our range of Biochemicals, please complete this form.
Legal Information
Brij is a registered trademark of Croda International PLC
ECO BRIJ is a registered trademark of Croda Inc.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Skin Irrit. 2
保管分類
11 - Combustible Solids
wgk
WGK 1
flash_point_f
>464.0 °F - Equilibrium method
flash_point_c
> 240 °C - Equilibrium method
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
第一種指定化学物質
prtr
STS0214-BULK: + STS0214-500G: + STS0214-100G: + STS0214-VAR:
jan
Yash Kapoor et al.
Journal of colloid and interface science, 322(2), 624-633 (2008-03-25)
Surfactants are commonly incorporated into hydrogels to increase solute loading and attenuate the release rates. In this paper we focus on understanding and modeling the mechanisms of both surfactant and drug transport in hydrogels. Specifically, we focus on Brij 98
Xi Chen et al.
Biochimica et biophysica acta, 1788(2), 477-483 (2009-01-03)
The size and the bilayer thickness of detergent-resistant membranes isolated from rat brain neuronal membranes using Triton X-100 or Brij 96 in buffers with or without the cations, K+/Mg2+ at a temperature of either 4 degrees C or 37 degrees
Carles Gil et al.
Biochemical and biophysical research communications, 348(4), 1334-1342 (2006-08-22)
Although the high presence of cholesterol in nerve terminals is well documented, specific roles of this lipid in transmitter release have remained elusive. Since cholesterol is a highly enriched component in the membrane microdomains known as lipid rafts, it is
Jia-You Fang et al.
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V, 67(1), 67-75 (2007-02-27)
Acoustically active lipospheres (AALs) were prepared using perfluorocarbons and coconut oil as the cores of inner phase. These AALs were stabilized using coconut oil and phospholipid coatings. A lipophilic antioxidant, resveratrol, was the model drug loaded into the AALs. AALs
Jessica Phelps et al.
Colloids and surfaces. B, Biointerfaces, 87(2), 391-398 (2011-06-28)
In this study, fluid precursor formulations for subcutaneous injection and in situ formation of hexagonal phase gels upon water absorption were developed as a strategy to sustain the release of naltrexone, a drug used for treatment of drug addiction. Precursor
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