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61689

Supelco

Methyl dodecanoate

analytical standard

Sinonimo/i:

Lauric acid methyl ester, Methyl laurate

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About This Item

Formula condensata:
CH3(CH2)10COOCH3
Numero CAS:
111-82-0
Peso molecolare:
214.34
Beilstein:
1767780
Numero CE:
203-911-3
Numero MDL:
MFCD00008966
Codice UNSPSC:
85151701
ID PubChem:
329759639
NACRES:
NA.24

Grado

analytical standard

Livello qualitativo

100

Saggio

≥99.5% (GC)

Durata

limited shelf life, expiry date on the label

tecniche

HPLC: suitable
gas chromatography (GC): suitable

Indice di rifrazione

n20/D 1.429-1.433

P. ebollizione

261-262 °C (lit.)

Punto di fusione

4.5-5 °C

Densità

0.869 g/mL at 20 °C (lit.)

Formato

neat

Gruppo funzionale

ester

Condizioni di spedizione

ambient

Temperatura di conservazione

room temp

Stringa SMILE

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
UQDUPQYQJKYHQI-UHFFFAOYSA-N

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Applicazioni

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

Prodotti consigliati

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.

Pittogrammi

Environment
GHS09

Avvertenze

Warning

Indicazioni di pericolo

H410

Consigli di prudenza

P273

Classi di pericolo

Aquatic Acute 1 - Aquatic Chronic 2

Codice della classe di stoccaggio

10 - Combustible liquids

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

282.2 °F - closed cup

Punto d’infiammabilità (°C)

139 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
BCCH1551
BCCC4869
BCBW6005
BCBX0156
BCBR9399V

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Methyl octanoate 99%

Sigma-Aldrich

260673

Methyl octanoate

Methyl myristate ≥99% (GC)

Sigma-Aldrich

M3378

Methyl myristate

Methyl decanoate ≥99%, FG

Sigma-Aldrich

W505501

Methyl decanoate

Methyl stearate analytical standard

Supelco

85769

Methyl stearate

Methyl pentadecanoate analytical standard

Supelco

76560

Methyl pentadecanoate

Methyl arachidate analytical standard

Supelco

10941

Methyl arachidate

Methyl cis-13-docosenoate analytical standard

Supelco

45659

Methyl cis-13-docosenoate

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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