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Sigma-Aldrich

N-Lauroylsarcosine sodium salt

≥97.0% (HPLC)

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Synonym(s):
N-Dodecanoyl-N-methylglycine sodium salt, Sarkosyl NL
Linear Formula:
CH3(CH2)10CON(CH3)CH2COONa
CAS Number:
137-16-6
Molecular Weight:
293.38
Beilstein:
5322974
EC Number:
205-281-5
MDL number:
MFCD00042728
UNSPSC Code:
12161902
PubChem Substance ID:
57651863
NACRES:
NA.22

description

anionic

Quality Level

200

Assay

≥97.0% (HPLC)

form

powder

mol wt

micellar avg mol wt 600

aggregation number

2

technique(s)

protein expression: suitable
protein purification: suitable
protein quantification: suitable

impurities

≤7% water

CMC

14.6 mM (20-25°C)

solubility

H2O: very soluble 293 g/L at 20 °C

SMILES string

[Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O

InChI

1S/C15H29NO3.Na/c1-3-4-5-6-7-8-9-10-11-12-14(17)16(2)13-15(18)19;/h3-13H2,1-2H3,(H,18,19);/q;+1/p-1

InChI key

KSAVQLQVUXSOCR-UHFFFAOYSA-M

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General description

N-Lauroylsarcosine is an anionic surfactant with an ability to denature proteins. Due to its microbicidal property, N-lauroylsarcosine is being considered as a potent anti-microbicide in topical formulations, especially against sexually transmitted diseases (STDs).

Application

N-Lauroylsarcosine sodium salt has been used to study the complexing ability of a novel amphiphilic γ-cyclodextrin with anionic surfactants.

Other Notes

Anionic surfactant.

Pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Signal Word

Danger

Hazard Statements

H315,H318,H330

Hazard Classifications

Acute Tox. 2 Inhalation - Eye Dam. 1 - Skin Irrit. 2

WGK

WGK 1

Flash Point(F)

closed cup

Flash Point(C)

closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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The mechanisms of herpes simplex virus (HSV) inactivation by sodium lauryl sulfate (SLS) and n-lauroylsarcosine (LS), two anionic surfactants with protein denaturant potency, have been evaluated in cultured cells. Results showed that pretreatment of HSV type 1 (HSV-1) strain F
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