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213721

Sigma-Aldrich

1,2-Dodecanediol

90%

Sinônimo(s):

1,2-Dihydroxydodecane, 1,2-Dodecylene glycol, 2-Hydroxylauryl alcohol, n-Dodecane-1,2-diol

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About This Item

Fórmula linear:
CH3(CH2)9CH(OH)CH2OH
Número CAS:
1119-87-5
Peso molecular:
202.33
Beilstein:
1700179
Número CE:
214-289-8
Número MDL:
MFCD00004726
Código UNSPSC:
12352100
ID de substância PubChem:
24852795
NACRES:
NA.22

Ensaio

90%

pf

56-60 °C (lit.)

cadeia de caracteres SMILES

CCCCCCCCCCC(O)CO

InChI

1S/C12H26O2/c1-2-3-4-5-6-7-8-9-10-12(14)11-13/h12-14H,2-11H2,1H3

chave InChI

ZITKDVFRMRXIJQ-UHFFFAOYSA-N

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Categorias relacionadas

Aplicação

1,2-Dodecanediol was used in the preparation of:
  • lipophilic diamines and amino alcohols
  • Fe(II), Co(II) and Ni(II) ferrite nanoparticles in the range of 9-25 nm

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 1

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)

Certificados de análise (COA)

Busque Certificados de análise (COA) digitando o Número do Lote do produto. Os números de lote e remessa podem ser encontrados no rótulo de um produto após a palavra “Lot” ou “Batch”.

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Recently, immunochromatography test strips (ICTS) have been fully developed for point-of-care testing (POCT). However, the intrinsic limitations including non-quantitative detection of colloidal gold ICTS and low sensitivity of fluorescence ICTS (FICTS) significantly restrict their further application in clinical diagnosis. Taking
Celso O R Júnior et al.
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A series of diamines and amino alcohols derived from 1-dodecanol, 1-tetradecanol, 1,2-dodecanediol and 1,2-tetradecanediol were synthesized and tested for their antitubercular activity. Compounds 3, 8 and 9 were found to be the most active (MIC of 6.25 microg/mL). Nine other
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We synthesized magnetic spinel ferrites from trimetallic single-source precursors. Fe(II), Co(II), and Ni(II) ferrite nanoparticles in the range of 9-25 nm were synthesized by solvothermal decomposition of trimetallic acetate complex precursors in benzyl ether in the presence of oleic acid
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