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Safety Information

L2136

Sigma-Aldrich

Lauric acid N,N-dimethylamide

~95%

Synonym(s):

N,N-Dimethyldodecanamide, N,N-Dimethyllauramide

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About This Item

Empirical Formula (Hill Notation):
C14H29NO
CAS Number:
3007-53-2
Molecular Weight:
227.39
EC Number:
221-117-5
MDL number:
MFCD00026554
UNSPSC Code:
12352211
PubChem Substance ID:
24896300

Assay

~95%

form

liquid

density

0.87 g/mL at 25 °C (lit.)

functional group

amide

shipped in

ambient

storage temp.

room temp

SMILES string

CCCCCCCCCCCC(=O)N(C)C

InChI

1S/C14H29NO/c1-4-5-6-7-8-9-10-11-12-13-14(16)15(2)3/h4-13H2,1-3H3

InChI key

BDYUSDIJIDGWCY-UHFFFAOYSA-N

Application

Dermal penetration enhancer; facilitates transport of solutes through the skin.

Pictograms

Environment
GHS09

Signal Word

Warning

Hazard Statements

H410

Precautionary Statements

P273 - P501

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

L2136-100G:
L2136-VAR:
L2136-50G:
L2136-10G:
L2136-25G:
L2136-BULK:

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Certificates of Analysis (COA)

Lot/Batch Number
107F5045
053F5077
077H5002

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B B Michniak et al.
Journal of pharmaceutical sciences, 82(2), 214-219 (1993-02-01)
A series of novel dermal penetration enhancers, esters and amides of clofibric acid, was synthesized. The permeation parameters and skin retention of two steroids (hydrocortisone-21-acetate and betamethasone-17-valerate) in propylene glycol were studied with athymic nude mouse skin by in vitro
Kuo-Yen Huang et al.
EMBO molecular medicine, 13(1), e12828-e12828 (2020-11-08)
To circumvent the devastating pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, a humanized decoy antibody (ACE2-Fc fusion protein) was designed to target the interaction between viral spike protein and its cellular receptor, angiotensin-converting enzyme 2 (ACE2).

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