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61689

Supelco

Methyl dodecanoate

analytical standard

Sinônimo(s):

Lauric acid methyl ester, Methyl laurate

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About This Item

Fórmula linear:
CH3(CH2)10COOCH3
Número CAS:
111-82-0
Peso molecular:
214.34
Beilstein:
1767780
Número CE:
203-911-3
Número MDL:
MFCD00008966
Código UNSPSC:
85151701
ID de substância PubChem:
329759639
NACRES:
NA.24

grau

analytical standard

Nível de qualidade

100

Ensaio

≥99.5% (GC)

prazo de validade

limited shelf life, expiry date on the label

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

índice de refração

n20/D 1.429-1.433

p.e.

261-262 °C (lit.)

pf

4.5-5 °C

densidade

0.869 g/mL at 20 °C (lit.)

Formato

neat

grupo funcional

ester

Condições de expedição

ambient

temperatura de armazenamento

room temp

cadeia de caracteres SMILES

CCCCCCCCCCCC(=O)OC

InChI

1S/C13H26O2/c1-3-4-5-6-7-8-9-10-11-12-13(14)15-2/h3-12H2,1-2H3

chave InChI

UQDUPQYQJKYHQI-UHFFFAOYSA-N

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Aplicação

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Produtos recomendados

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictogramas

Environment
GHS09

Palavra indicadora

Warning

Frases de perigo

H410

Declarações de precaução

P273

Classificações de perigo

Aquatic Acute 1 - Aquatic Chronic 2

Código de classe de armazenamento

10 - Combustible liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

282.2 °F - closed cup

Ponto de fulgor (°C)

139 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves

Escolha uma das versões mais recentes:

Certificados de análise (COA)

Lot/Batch Number
BCCH1551
BCCC4869
BCBW6005
BCBX0156
BCBR9399V

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Se precisar de uma versão específica, você pode procurar um certificado específico pelo número do lote ou da remessa.

Pesquise por COA

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Sigma-Aldrich

M3378

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Sigma-Aldrich

W505501

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Supelco

85769

Estearato de metila

Methyl pentadecanoate analytical standard

Supelco

76560

Methyl pentadecanoate

Methyl arachidate analytical standard

Supelco

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Methyl cis-13-docosenoate analytical standard

Supelco

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D A Dimas et al.
AAPS PharmSciTech, 1(2), E16-E16 (2004-01-20)
The effects of coating thickness, type of adhesive, and type and concentration of enhancer on the mechanical properties of two acrylic pressure-sensitive adhesives (PSAs) were investigated using a 2(4) factorial design and an optimization technique. Sixteen formulations containing 0% or
Y Komata et al.
Biological & pharmaceutical bulletin, 17(5), 705-708 (1994-05-01)
The effect of long chain fatty acid (FA) and its analogs on the accumulation of thiamine disulfide (TDS) in rat skin using propylene glycol as a vehicle was studied in vitro. Lauric acid (12:0) increased the accumulation of TDS in
E Barboza-Silva et al.
Oral microbiology and immunology, 24(4), 265-271 (2009-07-04)
The arginine deiminase system (ADS) of oral bacteria is a major generator of alkali (ammonia) in dental plaque and is considered to have anticaries effects. However, many of the antimicrobial agents used in oral care products may reduce alkali production
Néstor M Carballeira et al.
Lipids, 40(10), 1063-1068 (2005-12-31)
The hitherto unknown 2-methylsulfanyldecanoic acid and 2-methylsulfanyldodecanoic acid were synthesized from methyl decanoate and methyl dodecanoate, respectively, through the reaction of lithium diisopropylamide and dimethyldisulfide in THF followed by saponification with potassium hydroxide in ethanol. Both alpha-methylsulfanylated FA were cytotoxic
Tammar Hussein Ali et al.
Colloids and surfaces. B, Biointerfaces, 123, 981-985 (2014-12-04)
A series of sugar-based surfactants, involving a single hydrophobic chain (C12) and two side-by-side arranged head groups, was prepared form simple glucose precursors. All surfactants were highly water soluble and exhibited exclusively micellar assemblies. This behavior makes them interesting candidates
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