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157406

Sigma-Aldrich

2-Ethylhexanoyl chloride

98%

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About This Item

Linear Formula:
CH3(CH2)3CH(C2H5)COCl
CAS Number:
Molecular Weight:
162.66
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

0.72 mmHg ( 67.7 °C)

assay

98%

form

liquid

refractive index

n20/D 1.433 (lit.)

bp

67-68 °C/11 mmHg (lit.)

density

0.939 g/mL at 25 °C (lit.)

functional group

acyl chloride

SMILES string

CCCCC(CC)C(Cl)=O

InChI

1S/C8H15ClO/c1-3-5-6-7(4-2)8(9)10/h7H,3-6H2,1-2H3

InChI key

WFSGQBNCVASPMW-UHFFFAOYSA-N

Application

2-Ethylhexanoyl chloride was used in the preparation of 4-aza-6-ethyl-4-(2-ethylhexanoyloxy)-5-oxodecyl 2,3, 4,6-tetra-O-acetyl-l-thio-β-D glucopyranoside.[1] It was also used in the preparation of poly(4,8-bis-alkyloxybenzo(1,2-b:4,5-b′)dithiophene-2,6-diyl-alt-(alkyl thieno(3,4-b)thiophene-2-carboxylate)-2,6-diyl), having very promising photovoltaic properties.[2]

pictograms

Skull and crossbonesCorrosion

signalword

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 4 Oral - Met. Corr. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 1

flash_point_f

156.2 °F - closed cup

flash_point_c

69 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Spin-labelled glycolipid analogues: D-glucose series.
Tronchet JMJ, et al.
Carbohydrate Research, 275(2), 245-258 (1995)
Jianhui Hou et al.
Journal of the American Chemical Society, 131(43), 15586-15587 (2009-10-14)
HOMO level of the PBDTTT-based polymer was successfully reduced by introducing an ketone group in place of the ester group. The average PCE of the PBDTTT-based devices reached 6.3% with a champion PCE result of 6.58%. Due to its highly
Paul E Minkler et al.
Molecular genetics and metabolism, 120(4), 363-369 (2017-02-14)
While selectively quantifying acylcarnitines in thousands of patient samples using UHPLC-MS/MS, we have occasionally observed unidentified branched-chain C8 acylcarnitines. Such observations are not possible using tandem MS methods, which generate pseudo-quantitative acylcarnitine "profiles". Since these "profiles" select for mass alone

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