C73400
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:
Molecular Weight:
140.61
Beilstein:
507387
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Quality Level
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
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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Małgorzata Pamuła et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 26(33), 7374-7383 (2020-02-23)
The synthesis of tetramethoxyresorcinarene podands bearing p-toluene arms connected by -SO3 - (1) and -CH2 O- (2) linkers is presented herein. In the solid state, the resorcinarene podand 1 forms an intramolecular self-inclusion complex with the pendant p-toluene group of
Electrophilic attack at carbon-5 of guanine nucleosides: structure and properties of the resulting guanidinoimidazole products.
R C Moschel et al.
IARC scientific publications, (70)(70), 235-240 (1986-01-01)
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.
Nicholas R Oranzi et al.
Analytical chemistry, 91(6), 4092-4099 (2019-02-27)
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
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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