466387
Brij® S 100
average Mn ~4,670
别名:
聚氧乙烯(100)十八烷基醚
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关于此项目
线性分子式:
C18H37(OCH2CH2)nOH, n~100
化学文摘社编号:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
MDL number:
产品名称
Brij® S 100, average Mn ~4,670
SMILES string
O(CC[O])CCCCCCCCCCCCCCCCCC
InChI
1S/C20H41O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-19-22-20-18-21/h2-20H2,1H3
InChI key
PSEGVHKUPXNGGJ-UHFFFAOYSA-N
mol wt
average Mn ~4,670
mp
51-54 °C (lit.)
hydroxyl value
13‑25 mg KOH/g
solubility
propylene glycol and xylene: insoluble
density
1.1 g/mL at 25 °C (lit.)
HLB
18
Quality Level
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Application
Brij® S 100 可用于：
- 作为一种非离子表面活性剂研究其与鲁米诺的相互作用电化学发光用于生物分析
- 作为载体材料，利用气体饱和溶液（PGSS）工艺中的颗粒研究尼莫地平、非诺贝特和 邻香草醛的配方
- 作为浇铸溶液中的亲水性表面活性剂，制备不对称平板纳滤膜，并研究其对聚醚砜（PES）纳滤膜亲水性能的影响
Legal Information
Brij is a registered trademark of Croda International PLC
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Formulation of nimodipine, fenofibrate, and o-vanillin with Brij S100 and PEG 4000 using the PGSS process
Kravanja G, et al.
Journal of Supercritical Fluids, 135, 245-253 (2018)
S O Williams et al.
Drug development and industrial pharmacy, 26(1), 71-77 (2000-04-01)
The purpose of this study was to scale up an oil/water (o/w) cream formulation containing 40% diethylene glycol monoethyl ether (DGME), developed via 300-g laboratory batches in a 2(5-2) fractional factorial design, to 7-kg batch sizes in a Brogli-10 homogenizer.
Jae-Haeng Song et al.
Drug development and industrial pharmacy, 35(8), 897-903 (2009-02-26)
The oral administration of loratadine, an antihistamine, can have a variety of adverse side effects, such as headache, fatigue, and nausea, because of the transient high blood concentration. To avoid these effects, loratadine can be administered using a transdermal drug
J Q Zhang et al.
Drug delivery, 14(6), 381-387 (2007-08-19)
The study describes the development of stealth solid lipid nanoparticles (SLNs) as colloidal carriers for silibinin, a drug with very low solubility. Stealth SLNs were constituted mainly of bioacceptable and biodegradable lipids, such as stearic acid and surfactant Brij 78
Y C Lee et al.
Journal of pharmaceutical sciences, 86(4), 430-433 (1997-04-01)
An ocular insert is developed for the controlled systemic delivery of insulin. Commercially available Gelfoam absorbable gelatin sponge, USP, is used in the fabrication of the ocular insert in the form of a matrix system. Two eyedrop formulations and 13
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