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B83606

Sigma-Aldrich

4-Methylbenzyl bromide

97%

Synonym(s):

p-Xylyl bromide

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About This Item

Linear Formula:
CH3C6H4CH2Br
CAS Number:
104-81-4
Molecular Weight:
185.06
Beilstein:
507389
EC Number:
203-240-6
MDL number:
MFCD00000181
UNSPSC Code:
12352100
PubChem Substance ID:
24891943
NACRES:
NA.22

Assay

97%

form

powder

impurities

<1.5% 1,4-bis(bromomethyl)benzene

bp

218-220 °C (lit.)

mp

34-36 °C (lit.)

storage temp.

2-8°C

SMILES string

Cc1ccc(CBr)cc1

InChI

1S/C8H9Br/c1-7-2-4-8(6-9)5-3-7/h2-5H,6H2,1H3

InChI key

WZRKSPFYXUXINF-UHFFFAOYSA-N

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Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

208.4 °F - closed cup

Flash Point(C)

98 °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.

JAN Code

B83606-100G:
B83606-BULK:
B83606-25G:
B83606-VAR:
B83606-1KG:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Sigma-Aldrich

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Zhouyang Li et al.
Talanta, 174, 198-205 (2017-07-26)
This paper reports novel imidazole fluorescent poly(ionic liquid) nanoparticles (FPILNs) of poly(1-[(4-methyphenyl)methyl]-3-vinyl-imidazolium bromide (poly([MVI]Br) for selective and sensitive determination of pyrogallol. An imidazole ionic liquid of 1-[(4-methyphenyl)methyl]-3-vinyl-imidazolium bromide ([MVI]Br) was synthesized and used as the only monomer to obtain poly([MVI]Br)
Ngoc-Duc Doan et al.
Journal of peptide science : an official publication of the European Peptide Society, 21(5), 387-391 (2014-11-18)
The solid-phase synthesis of azapeptides possessing a C-terminal aza-residue has been accomplished by a protocol featuring regioselective alkylation of benzhydrylidene-aza-glycinamide and illustrated by the syntheses of [aza-Lys(6)] growth-hormone-releasing peptide-6 analogs.

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