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Merck
CN

15S7

TERGITOL

greener alternative

Type 15-S-7

Synonym(s):

Secondary alcohol ethoxylate

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About This Item

NACRES:
NA.25
UNSPSC Code:
12161900
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Product Name

TERGITOL, Type 15-S-7

description

non-ionic

type

Type 15-S-7

form

liquid

mol wt

508 g/mol

greener alternative product characteristics

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

sustainability

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CMC

38 ppm

transition temp

pour point 1 °C
cloud point 37 °C

HLB

12.1

greener alternative category

Quality Level

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Application

Tergitol 15-S-7 has been used:
  • To study the synergistic effect of Tergitol 15-S-7 and AOT (dioctyl sulfosuccinate) on bacterial oxidation of alkanes in crude oils
  • In cloud-point extraction technique to extract polycyclic aromatic hydrocarbons from aqueous solutions
  • Along with MgSO4 in anolyte reservoir for electrokinetic experiments
  • As a very efficient surfactant in removing non-polar oil
  • To study the phase behavior of surfactant-brine–oil system, which is desired for enhanced oil recovery

Features and Benefits

  • Excellent formulation & handling properties
  • Superior wetting & rinseability
  • Low odor
  • Narrow gel range

General description

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 biodegradable surfactant and is aligned with the 10th principle of Green Chemistry "Design for Degradation".

Tergitol 15-S-7 is a linear non-ionic surfactant that is a secondary ethoxylated alcohol. It is compatible with anionic, cationic, and other nonionic surfactants.

Legal Information

TERGITOL is a trademark of The Dow Chemical Company ("Dow") or an affiliated company of Dow

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

469.4 °F - open cup

flash_point_c

243 °C - open cup

ppe

Eyeshields, Gloves, type N95 (US)


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Determination of estrogens in human urine by high-performance liquid chromatography/diode array detection with ultrasound-assisted cloud-point extraction.
Zou Y, et al.
Analytical Biochemistry, 421(2), 378-384 (2012)
Effects of surfactant mixtures, including Corexit 9527, on bacterial oxidation of acetate and alkanes in crude oil.
Bruheim P, et al.
Applied and Environmental Microbiology, 65(4), 1658-1661 (1999)
Rates of solubilization of triolein into nonionic surfactant solutions.
Chen BH, et al.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 128(1-3), 129-143 (1997)
Effects of additives on the cloud points of selected nonionic linear ethoxylated alcohol surfactants.
Li J L, et al.
Colloids and Surfaces. A, Physicochemical and Engineering Aspects, 346(1-3), 237-243 (2009)
Behavior of surfactant mixtures in model oily-soil detergency studies.
Aronson M P, et al.
Journal of the American Oil Chemists' Society, 60(7), 1333-1339 (1983)

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