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174866

Sigma-Aldrich

1,12-Dibromododecane

98%

Sinónimos:

Dodecamethylene dibromide

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About This Item

Fórmula lineal:
Br(CH2)12Br
Número de CAS:
3344-70-5
Peso molecular:
328.13
Beilstein/REAXYS Number:
1742763
EC Number:
222-096-5
MDL number:
MFCD00000226
UNSPSC Code:
12352100
PubChem Substance ID:
24850357
NACRES:
NA.22

assay

98%

form

solid

bp

215 °C/15 mmHg (lit.)

mp

38-42 °C (lit.)

SMILES string

BrCCCCCCCCCCCCBr

InChI

1S/C12H24Br2/c13-11-9-7-5-3-1-2-4-6-8-10-12-14/h1-12H2

Inchi Key

ZJJATABWMGVVRZ-UHFFFAOYSA-N

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Application

1,12-Dibromododecane was used in the preparation of tboc-protected ionenes.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sean M Ramirez et al.
Macromolecular bioscience, 9(11), 1127-1134 (2009-07-29)
Novel tboc-protected ionenes with M(w) exceeding 30 kDa were prepared from the step-growth polymerization of tert-butyl bis[3-(dimethylamino)propyl]carbamate and 1,12-dibromododecane. The protected ionenes yielded pH-sensitive, protonatable ionenes with pK(a) approximately 6.6 for the conjugate acid of the protonated secondary amine. Polyplexes
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The synthesis and characteristics are presented of novel double-salt herbicidal ionic liquids (DSHILs) that contain 4-chloro-2-methylphenoxyacetate and trans-cinnamate anions. In the designed synthesis, an anion of natural origin and a herbicidal anion were combined with an amphiphilic bisammonium cation to
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