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305626

Sigma-Aldrich

Hexylphosphonic dichloride

95%

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About This Item

Linear Formula:
CH3(CH2)5P(O)Cl2
CAS Number:
928-64-3
Molecular Weight:
203.05
MDL number:
MFCD00010386
UNSPSC Code:
12352100
PubChem Substance ID:
24858443
NACRES:
NA.22

assay

95%

form

liquid

refractive index

n20/D 1.465 (lit.)

bp

114-121 °C/16 mmHg (lit.)

density

1.185 g/mL at 25 °C (lit.)

SMILES string

CCCCCCP(Cl)(Cl)=O

InChI

1S/C6H13Cl2OP/c1-2-3-4-5-6-10(7,8)9/h2-6H2,1H3

InChI key

GZXBQDURAKBNAZ-UHFFFAOYSA-N

Related Categories

Application

Hexylphosphonic dichloride was used in preparation of:
  • hexylphosphonic acid via reaction with water
  • phosphonate esters
  • methyl 4-methylumbelliferyl hexylphosphonate

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

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

Certificates of Analysis (COA)

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Active-site titration analysis of surface influences on immobilized< i> Candida antarctica</i> lipase B activity.
Laszlo JA, et al.
Journal of Molecular Catalysis. B, Enzymatic, 69(1), 60-65 (2011)
Mechanisms of the shape evolution of CdSe nanocrystals.
Peng ZA and Peng X.
Journal of the American Chemical Society, 123(7), 1389-1395 (2001)
Alessandra Mezzetti et al.
Chemistry & biology, 12(4), 427-437 (2005-04-27)
Synthetic chemists often exploit the high enantioselectivity of lipases to prepare pure enantiomers of primary alcohols, but the molecular basis for this enantioselectivity is unknown. The crystal structures of two phosphonate transition-state analogs bound to Burkholderia cepacia lipase reveal this

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