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4-Methoxybenzyl Chloride (stabilized with Potassium carbonate) - >98.0%(GC)(T), high purity , CAS No.824-94-2

COA

Grade & Purity:

≥98%(GC)(T)

Cas Number: 824-94-2
Molecular Weight: 156.61
Beilstein Registry Number: 6(4)2137
PubChem CID: 69993
PubChem SID: 504754474

In stock

Item Number

M491599

Grouped product items
SKU	Size	Availability	Price
M491599-5ml	5ml	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$9.90
M491599-25ml	25ml	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$39.90
M491599-100ml	100ml	4	$69.90
M491599-500ml	500ml	Available within 4-8 weeks(?) Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!	$169.90

View related series

ether (317) Heterocyclic block (497)

Basic Description

Synonyms	4methoxybenzyl chloride \| 4-Methoxybenzyl chloride \| 4-methoxy-benzyl chloride \| DTXSID20231718 \| EINECS 212-540-6 \| NSC172955 \| NSC-172955 \| para-methoxybenzylchloride \| W-104172 \| 1-(chloro methyl)-4-methoxybenzene \| Benzene, 1-(chloromethyl)-4-methoxy-
Specifications & Purity	≥98%(GC)(T)
Storage Temp	Store at 2-8°C,Argon charged
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Product Description	4-Methoxybenzyl chloride can be used as a reactant: To synthesize 4-methoxybenzyl esters by reacting with cyclic anhydrides. In the mono-alkylation of trans-1,2-diaminocyclohexane. It can also be used as a: Protecting group for amino acids during peptide synthesis using triethylamine as a base. Co-catalyst in the intramolecular carboamination of aminodienes to N-heterocyclesvia benzyl-group transfer.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Benzyl halides

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Benzyl halides
Intermediate Tree Nodes	Not available
Direct Parent	Benzyl chlorides
Alternative Parents	Phenoxy compounds Methoxybenzenes Anisoles Alkyl aryl ethers Organochlorides Hydrocarbon derivatives Alkyl chlorides
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Phenoxy compound - Methoxybenzene - Benzyl chloride - Phenol ether - Anisole - Alkyl aryl ether - Ether - Organic oxygen compound - Hydrocarbon derivative - Organooxygen compound - Organochloride - Organohalogen compound - Alkyl halide - Alkyl chloride - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as benzyl chlorides. These are organic compounds containing a benzene skeleton substituted with a chloromethyl group.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	504754474
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504754474
IUPAC Name	1-(chloromethyl)-4-methoxybenzene
INCHI	InChI=1S/C8H9ClO/c1-10-8-4-2-7(6-9)3-5-8/h2-5H,6H2,1H3
InChIKey	MOHYOXXOKFQHDC-UHFFFAOYSA-N
Smiles	COC1=CC=C(C=C1)CCl
Isomeric SMILES	COC1=CC=C(C=C1)CCl
Molecular Weight	156.61
Beilstein	6(4)2137
Reaxy-Rn	606667
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=606667&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

18 results found

Lot Number	Certificate Type	Date	Item
F2512574	Certificate of Analysis	May 30, 2025	M491599
F2512613	Certificate of Analysis	May 30, 2025	M491599
F2512614	Certificate of Analysis	May 30, 2025	M491599
C2524621	Certificate of Analysis	Nov 06, 2024	M491599
C2518245	Certificate of Analysis	Nov 06, 2024	M491599
K2414611	Certificate of Analysis	Nov 06, 2024	M491599
K2414612	Certificate of Analysis	Nov 06, 2024	M491599
K2414617	Certificate of Analysis	Nov 06, 2024	M491599
K2414618	Certificate of Analysis	Nov 06, 2024	M491599
K2414631	Certificate of Analysis	Nov 06, 2024	M491599
H2308094	Certificate of Analysis	Jul 19, 2023	M491599
H2308099	Certificate of Analysis	Jul 19, 2023	M491599
H2308119	Certificate of Analysis	Jul 19, 2023	M491599
H2308091	Certificate of Analysis	Jul 19, 2023	M491599
H2308088	Certificate of Analysis	Jul 19, 2023	M491599
J2228574	Certificate of Analysis	Sep 05, 2022	M491599
J2228589	Certificate of Analysis	Sep 05, 2022	M491599
J2228590	Certificate of Analysis	Sep 05, 2022	M491599

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Chemical and Physical Properties

Sensitivity	Moisture sensitive；Heat sensitive
Refractive Index	1.547
Flash Point(°F)	228.2 °F
Flash Point(°C)	109°C
Boil Point(°C)	127°C/24mmHg
Molecular Weight	156.610 g/mol
XLogP3	2.400
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	2
Exact Mass	156.034 Da
Monoisotopic Mass	156.034 Da
Topological Polar Surface Area	9.200 Å²
Heavy Atom Count	10
Formal Charge	0
Complexity	87.300
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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