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526126

Sigma-Aldrich

4-(Chloromethyl)benzyl alcohol

99%

Synonym(s):

1-(Chloromethyl)-4-(hydroxymethyl)benzene, 4-(Chloromethyl)benzenemethanol, 4-Chloromethylbenzyl alcohol, 4-Hydroxymethylbenzyl chloride, [4-(Chloromethyl)phenyl]methanol, p-(Chloromethyl)benzyl alcohol, p-(Hydroxymethyl)benzyl chloride

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About This Item

Linear Formula:
ClCH2C6H4CH2OH
CAS Number:
16473-35-1
Molecular Weight:
156.61
MDL number:
MFCD03427011
UNSPSC Code:
12352100
PubChem Substance ID:
24874535
NACRES:
NA.22
Pricing and availability is not currently available.

Assay

99%

mp

58-60 °C (lit.)

functional group

chloro
hydroxyl

SMILES string

OCc1ccc(CCl)cc1

InChI

1S/C8H9ClO/c9-5-7-1-3-8(6-10)4-2-7/h1-4,10H,5-6H2

InChI key

OGALXJIOJZXBBP-UHFFFAOYSA-N

Related Categories

General description

4-(Chloromethyl)benzyl alcohol can be synthesized from 4-(chloromethyl)benzoyl chloride.[1]

Application

4-(Chloromethyl)benzyl alcohol may be used in the synthesis of 4-(chloromethyl)benzyl acetate.[2]

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SHBR9837
SHBF9621V
SHBF3235V
SHBD5980V
SHBC2746V

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Aoyagi N and Endo T.
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Fire properties of polystyrene-clay nanocomposites.
Zhu J, et al.
Chemistry of Materials, 13(10), 3774-3780 (2001)
Milada Šírová et al.
Journal of drug targeting, 25(9-10), 796-808 (2017-07-21)
Polymer carriers based on N-(2-hydroxypropyl)methacrylamide (HPMA) copolymers with incorporated organic nitrates as nitric oxide (NO) donors were designed with the aim to localise NO generation in solid tumours, thus highly increasing the enhanced permeability and retention (EPR) effect. The NO
Rodolfo M Moraes et al.
Polymers, 12(6) (2020-06-04)
Well-defined amphiphilic, biocompatible and partially biodegradable, thermo-responsive poly(N-vinylcaprolactam)-b-poly(ε-caprolactone) (PNVCL-b-PCL) block copolymers were synthesized by combining reversible addition-fragmentation chain transfer (RAFT) and ring-opening polymerizations (ROP). Poly(N-vinylcaprolactam) containing xanthate and hydroxyl end groups (X-PNVCL-OH) was first synthesized by RAFT/macromolecular design by the

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