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305626

Sigma-Aldrich

Hexylphosphonic dichloride

95%

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1 G
¥14,480

¥14,480

Estimated to ship onMay 30, 2025

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1 G
¥14,480

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

¥14,480

Estimated to ship onMay 30, 2025

Request a Bulk Order

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.)

functional group

phosphine oxide

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[1]
  • phosphonate esters[2]
  • methyl 4-methylumbelliferyl hexylphosphonate[3]

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302 + H312 + H332,H314

Hazard Classifications

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

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid

JAN Code

305626-VAR:
305626-BULK:
305626-1G:
305626-100G:
305626-5G:

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Certificates of Analysis (COA)

Lot/Batch Number
MKCM8151
MKCL5604
MKCK9799
MKCK9509
MKCK3397

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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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