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Merck

388831

SP Brij® C2 MBAL-SO-(SG)

average Mn ~330

Synonym(s):

Brij® 52, Polyethylene glycol hexadecyl ether, Polyoxyethylene (2) cetyl ether

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About This Item

Linear Formula:
C16H33(OCH2CH2)nOH, n~2
CAS Number:
9004-95-9
MDL number:
MFCD00080892
UNSPSC Code:
12162002
PubChem Substance ID:
24864248
NACRES:
NA.23
Beilstein/REAXYS Number:
1867431

Key Documents

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Product Name

SP Brij® C2 MBAL-SO-(SG), average Mn ~330

SMILES string

CCCCCCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO

InChI

1S/C56H114O21/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-17-58-19-21-60-23-25-62-27-29-64-31-33-66-35-37-68-39-41-70-43-45-72-47-49-74-51-53-76-55-56-77-54-52-75-50-48-73-46-44-71-42-40-69-38-36-67-34-32-65-30-28-63-26-24-61-22-20-59-18-16-57/h57H,2-56H2,1H3

InChI key

NLMKTBGFQGKQEV-UHFFFAOYSA-N

vapor pressure

0.26 psi ( 20 °C)

form

solid

mol wt

average Mn ~330

refractive index

n20/D 1.466 (lit.)

density

0.978 g/mL at 25 °C (lit.)

HLB

5

Quality Level

200

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Legal Information

Brij is a registered trademark of Croda International PLC

pictograms

Environment
GHS09

hcodes

H411

Hazard Classifications

Aquatic Chronic 2

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

302.0 °F - closed cup

flash_point_c

150 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCP0416
BCCJ5781
BCCG6514
BCCD0444
BCBV5468

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Anja Heins et al.
Lipids, 42(6), 561-572 (2007-04-21)
The location and the resulting chemical microenvironment of the antioxidant propyl gallate (PG) was studied in micellar solutions using the cationic emulsifier cetyl trimethyl ammonium bromide (CTAB), the anionic emulsifier sodium dodecyl sulphate (SDS) and the non-ionic emulsifier Brij 58
G Tataru et al.
International journal of pharmaceutics, 404(1-2), 83-93 (2010-11-16)
Magnetic micro- and nanoparticles based on ferrofluid (maghemite) were elaborated by inverse emulsion crosslinking of sodium salt of carboxymethylcellulose (CMCNa) and gelatin. Crosslinking was carried out with glutaric aldehyde within aqueous droplets dispersed into toluene in presence of surfactants. The
Sreekhar Cheboyina et al.
International journal of pharmaceutics, 359(1-2), 167-173 (2008-05-23)
A novel freeze pelletization technique was evaluated for the preparation of wax-based sustained release matrix pellets. Pellets containing water-soluble drugs were successfully prepared using a variety of waxes. The drug release significantly depended on the wax type used and the
Xue Li et al.
Chemosphere, 78(6), 752-759 (2009-12-17)
Currently, soil contamination by polybrominated diphenyl ethers (PBDEs) at e-waste recycling sites in China is of significant environmental concern and requires the identification of appropriate remediation technologies. In this paper, photodestruction of a model PBDE congener (BDE-99) in selected UV/surfactant
Yuji Ishii et al.
Drug metabolism and disposition: the biological fate of chemicals, 40(11), 2081-2089 (2012-08-02)
We have suggested that adenine-related compounds are allosteric inhibitors of UGT in rat liver microsomes (RLM) treated with detergent. To clarify whether the same occurs with a pore-forming peptide, alamethicin, the effects of adenine-related compounds on 4-metylumbelliferone (4-MU) glucuronidation were
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