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Sigma-Aldrich

Rhamnolipids

greener alternative

90%

Synonym(s):

Rhamnolipids

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About This Item

UNSPSC Code:
12352211
NACRES:
NA.22

product name

Rhamnolipids, 90%,

biological source

Pseudomonas aeruginosa

Quality Level

form

solid/granular

greener alternative product characteristics

Design for Degradation: Greener alternative product characteristics
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

greener alternative category

shipped in

ambient

storage temp.

room temp

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General description

Rhamnolipid biosurfactants are glycolipids containing L-rhamnose and ß-hydroxyl fatty acids, with amphiphilic properties (both hydrophilic and hydrophobic). This rhamnolipid product has been purified from Pseudomonas aeruginosa and contains a mixture of rhamnolipids with fatty acids of varying tail length. They are highly biodegradable, non-toxic, and renewable. Functional roles include bioactive, surfactant and emulsifier. Rhamnolipids provide good detergency/foaming/wetting, stable microemulsion formation, and solubility under high alkalinity. They are mild with skin-friendly attributes. Surfactant and emulsion properties of rhamnolipids include reducing the surface tension of water to 25 to 40 mN/m, having a CMC of 5-380 mg/L, and decreasing the interfacial tension of oil and water to <1 dyne/cm. Rhamnolipid biosurfactants are superior to synthetic surfactants for several reasons: their CMC is 10-100 times lower than that of traditional chemical surfactants (meaning much less material is required to achieve reductions in surface tension/interfacial tension); they are easily biodegradable with very low toxicity (having higher EC50 values); they are not as affected by temperature, pH and salinity; and they are sustainably produced.

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for hydrocarbon degradation. For more information see the paper Environmental applications of biosurfacants: recent advances, and the many other articles available at: AGAE Technologies

Application

Rhamnolipids can be used in pharmaceuticals, cosmeceuticals, cosmetics, personal products, environmental bioremediation, the petroleum industry, household cleaners, food and beverage processing, agriculture and horticulture, therapeutics, nanotechnology, the polymer industry, cryo-protectants, the mining industry, biofuels, ethanol production, microbial fuel cells, protein research, and neural stem cell studies.

Legal Information

Product of AGAE Technologies

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

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Ibukun O Olasanmi et al.
Journal of advanced research, 21, 79-90 (2020-02-20)
Environmental pollution by petroleum hydrocarbons (PHCs) is a severe and widespread problem impacting human health and the environment. To combat this issue, innovative and sustainable treatment methods are required. This research study investigated rhamnolipid-enhanced washing of drill cuttings and petroleum-contaminated
Irene E Samonte-Padilla et al.
BMC developmental biology, 11, 55-55 (2011-09-14)
Rapid advances in genomics have provided nearly complete genome sequences for many different species. However, no matter how the sequencing technology has improved, natural genetic polymorphism complicates the production of high quality reference genomes. To address this problem, researchers have
Bartosz Gerard Gdaniec et al.
Environmental microbiology, 22(8), 3572-3587 (2020-06-24)
Interspecies bacterial competition may occur via cell-associated or secreted determinants and is key to successful niche colonization. We previously evolved Pseudomonas aeruginosa in the presence of Staphylococcus aureus and identified mutations in the Wsp surface-sensing signalling system. Surprisingly, a ΔwspF
[Factor VIII inhibitor postpartum].
I Ohkubo et al.
[Rinsho ketsueki] The Japanese journal of clinical hematology, 27(9), 1596-1602 (1986-09-01)
Metabolism of isoprenaline in the intestine.
C F George et al.
The Journal of pharmacy and pharmacology, 26(4), 265-267 (1974-04-01)

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