Sodium dodecanoate

Inquiry

Molecular Formula:

C12H23NaO2

Molecular Weight:

222.30

CAS Number:

629-25-4

Catalog Number:

629-25-4

Product Information

Molecular Formula:

C12H23NaO2

Molecular Weight:

222.30

Description

Sodium dodecanoate is an organic sodium salt resulting from the replacement of the proton from the carboxy group of dodecanoic acid by a sodium ion. It has a role as a detergent. It contains a dodecanoate.

Synonyms

Dodecanoic acid sodium salt, Lauric acid sodium salt, Sodium laurate

IUPAC Name

sodiumdodecanoate

Canonical SMILES

CCCCCCCCCCCC(=O)[O-].[Na+]

InChI

InChI=1S/C12H24O2.Na/c1-2-3-4-5-6-7-8-9-10-11-12(13)14/h2-11H2,1H3,(H,13,14)/q+1/p-1

InChI Key

BTURAGWYSMTVOW-UHFFFAOYSA-M

Boiling Point

296.1°C at 760 mmHg

Melting Point

43.8°C

Flash Point

134.1°C

Purity

95%

Solubility

water, 3244 mg/L @ 25 °C (est)

Appearance

slightly yellow powder

Application

Used as an anticaking agent, lubricant or release agent, and emulsifier for foods; Used as a laboratory chemical and intermediate.

Stability

Stable. Combustible. Incompatible with strong oxidizing agents, strong bases, strong acids. May be moisture sensitive.

Safety Information

Hazards

H315:
Causes skin irritation.
H318:
Causes serious eye damage.
H411:
Toxic to aquatic life with long-lasting effects.

Precautionary Statement

P264:
Wash thoroughly after handling.
P273:
Avoid release to the environment.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P305+P351+P338+P310:
IF IN EYES:
Rinse cautiously with water for several minutes.
Remove contact lenses if present and easy to do. Continue rinsing.
Immediately call a POISON CENTER or doctor/physician.
P391:
Collect spillage.
P501:
Dispose of contents/container in accordance with local/regional/national/international regulations.

Computed Properties

Hydrogen Bond Donor Count

Hydrogen Bond Acceptor Count

Rotatable Bond Count

Exact Mass

222.15957425 g/mol

Monoisotopic Mass

222.15957425 g/mol

Topological Polar Surface Area

40.1Å²

Heavy Atom Count

Formal Charge

Complexity

138

Isotope Atom Count

Defined Atom Stereocenter Count

Undefined Atom Stereocenter Count

Defined Bond Stereocenter Count

Undefined Bond Stereocenter Count

Covalently-Bonded Unit Count

Compound Is Canonicalized

Yes

Patents

Publication Number	Title	Priority Date
CN-114058220-A	Antibacterial and mildewproof coating and preparation method and application thereof	2021-12-31
CN-114085588-A	Allyl polyoxyethylene ether phosphate modified acrylic resin water-based paint	2021-12-15
CN-114029050-A	Synthesis method of supported high-load carbon-coated noble metal nanoparticle catalyst	2021-12-13
CN-114163884-A	Waterproof anti-slip coating special for outer wall and preparation method and application thereof	2021-12-10
CN-114105152-A	Preparation method of nano white carbon black	2021-11-30
CN-113973817-A	Compound insecticidal composition containing D-limonene and fluorine lice sulfanilamide and application thereof	2021-11-25
CN-113956555-A	Low-temperature-resistant, antioxidant and flame-retardant sheath material and preparation method thereof	2021-11-17
CN-113862820-A	Three-dimensional crimped polyester fiber, fabric and application of fabric in pillow, quilt or mattress filling material	2021-11-15
CN-113832710-A	Anti-wrinkle fabric and preparation method thereof	2021-11-12
CN-113943509-A	Environment-friendly long-life anti-fouling stone-like paint and preparation method thereof	2021-11-09

Literatures

PMID	Publication Date	Title	Journal
34506767	2021-10-01	Lauric acid alleviates deoxynivalenol-induced intestinal stem cell damage by potentiating the Akt/mTORC1/S6K1 signaling axis	Chemico-biological interactions
28729181	2017-09-01	Expression of CYP4V2 in human THP1 macrophages and its transcriptional regulation by peroxisome proliferator-activated receptor gamma	Toxicology and applied pharmacology
22795601	2012-11-01	Bioactive constituents in Prunus africana: geographical variation throughout Africa and associations with environmental and genetic parameters	Phytochemistry
22854496	2012-10-01	Cyclic glycolipids from glandular trichome exudates of Cerastium glomeratum	Phytochemistry
22922311	2012-10-01	A series of hybrid P450 BM3 enzymes with different catalytic activity in the light-initiated hydroxylation of lauric acid	Journal of inorganic biochemistry
22920263	2012-09-26	Efficient solvent-free synthesis of phytostanyl esters in the presence of acid-surfactant-combined catalyst	Journal of agricultural and food chemistry
22890798	2012-09-24	Rates of fatty acid oxidations by P450 compound I are pH dependent	Chembiochem : a European journal of chemical biology
22876990	2012-08-21	Single molecule dynamics on hydrophobic self-assembled monolayers	Langmuir : the ACS journal of surfaces and colloids
22252881	2012-07-01	BESSICC, a COSMO-RS based tool for in silico solvent screening of biocatalyzed reactions	Biotechnology and bioengineering
23077821	2012-07-01	Activity of virgin coconut oil, lauric acid or monolaurin in combination with lactic acid against Staphylococcus aureus	The Southeast Asian journal of tropical medicine and public health

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

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The dilution calculator equation

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

This equation is commonly abbreviated as: C₁V₁ = C₂V₂

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