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105740

Sigma-Aldrich

α,α′-Dichloro-p-xylene

98%

Synonym(s):

1,4-Bis(chloromethyl)benzene, p-Xylylene dichloride

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About This Item

Linear Formula:
C6H4(CH2Cl)2
CAS Number:
623-25-6
Molecular Weight:
175.06
Beilstein:
774706
EC Number:
210-782-7
MDL number:
MFCD00000920
UNSPSC Code:
12352100
PubChem Substance ID:
24846708
NACRES:
NA.22

Assay

98%

form

solid

bp

254 °C (lit.)

mp

98-101 °C (lit.)

functional group

chloro

SMILES string

ClCc1ccc(CCl)cc1

InChI

1S/C8H8Cl2/c9-5-7-1-2-8(6-10)4-3-7/h1-4H,5-6H2

InChI key

ZZHIDJWUJRKHGX-UHFFFAOYSA-N

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General description

α,α′-Dichloro-p-xylene undergoes phase transfer catalysed polycondensation with t-butylcyanoacetate to form carbon-carbon chain polymer.

Application

α,α′-Dichloro-p-xylene is a monomer used in preparation of poly(p-phenylene vinylene(PPV) nanotubes and nanorods by chemical vapor deposition (CVD) polymerization method. α,α′-Dichloro-p-xylene was used in a study to investigate the effect of CVD monomer selection and reaction conditions on the resulting PPV polymer layer composition and luminescence properties.

Pictograms

Skull and crossbonesEnvironment
GHS06,GHS09

Signal Word

Danger

Hazard Statements

H315,H317,H330,H410

Hazard Classifications

Acute Tox. 2 Inhalation - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2 - Skin Sens. 1A

Storage Class Code

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

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
WXBF1589V
MKCT6704
MKCR5796
MKCK3386
MKCD0277

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Synthesis of carbon-carbon chain polymer by phase-transfer-catalyzed polycondensation of α, α'-dichloro-p-xylene with t-butyl cyanoacetate.
Imai Y, et al.
Journal of Polymer Science - Part C: Polymer Letters, 19(4), 205-210 (1981)
Preparation of PPV nanotubes and nanorods and carbonized products derived therefrom.
Kim K and Jin J.
Nano Letters, 1(11), 205-210 (1981)
Poly (p-phenylene vinylene) prepared by chemical vapor deposition: Influence of monomer selection and reaction conditions on film composition and luminescence properties.
Vaeth KM and Jensen KF.
Macromolecules, 31(20), 6789-6793 (1998)
Contact dermatitis caused by "chloromethyl heterocyclic intermediates".
H Ippen
Contact dermatitis, 16(1), 52-52 (1987-01-01)
Jing-Wei Xu et al.
Colloids and surfaces. B, Biointerfaces, 133, 148-155 (2015-06-22)
Electrospun nanofibers with antibacterial activity are greatly promising for medical treatment and water purification. Herein we report antibacterial nanofibers electrospun from a series of poly(dimethylamino ethyl methacrylate-co-alkyl methacrylates) (poly(DMAEMA-co-AMA)) and to distinguish the effects of free and cross-linked cations derived

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