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C73400

Sigma-Aldrich

4-Methylbenzyl chloride

98%

Synonym(s):

α-Chloro-p-xylene, p-Xylyl chloride

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About This Item

Linear Formula:
CH3C6H4CH2Cl
CAS Number:
104-82-5
Molecular Weight:
140.61
Beilstein:
507387
EC Number:
203-241-1
MDL number:
MFCD00000919
UNSPSC Code:
12352100
PubChem Substance ID:
24892958
NACRES:
NA.22

Quality Level

100

Assay

98%

form

liquid

refractive index

n20/D 1.533 (lit.)

bp

200 °C (lit.)

mp

4 °C (lit.)

density

1.062 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

Cc1ccc(CCl)cc1

InChI

1S/C8H9Cl/c1-7-2-4-8(6-9)5-3-7/h2-5H,6H2,1H3

InChI key

DMHZDOTYAVHSEH-UHFFFAOYSA-N

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Related Categories

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302 - H314

Hazard Classifications

Acute Tox. 4 Oral - Skin Corr. 1B

Storage Class Code

8A - Combustible, corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

167.0 °F - closed cup

Flash Point(C)

75 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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IARC scientific publications, (70)(70), 235-240 (1986-01-01)
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Quantitation of the serum concentration of 25-hydroxyvitamin D is a high-demand assay that suffers from long chromatography time to separate 25-hydroxyvitamin D from its inactive epimer; however, ion mobility spectrometry can distinguish the epimer pair in under 30 ms due
K Hemminki et al.
Journal of applied toxicology : JAT, 3(4), 203-207 (1983-08-01)
Benzyl chloride, benzyl bromide, p-methylbenzyl chloride, and p-nitrobenzyl chloride were used to study chemical reactivity with 4-(p-nitrobenzyl)-pyridine (NBP), and with guanosine in vitro, in relation to mutagenic potency in S. typhimurium and sister chromatid exchange (SCE) induction in CHO cells.
Enis Nadia Md Yusof et al.
International journal of molecular sciences, 20(4) (2019-02-20)
Six new organotin(IV) compounds of Schiff bases derived from S-R-dithiocarbazate [R = benzyl (B), 2- or 4-methylbenzyl (2M and 4M, respectively)] condensed with 2-hydroxy-3-methoxybenzaldehyde (oVa) were synthesised and characterised by elemental analysis, various spectroscopic techniques including infrared, UV-vis, multinuclear (¹H
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