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About This Item
Linear Formula:
CH3(CH2)7OCH2Cl
CAS Number:
Molecular Weight:
178.70
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
95%
InChI
1S/C9H19ClO/c1-2-3-4-5-6-7-8-11-9-10/h2-9H2,1H3
SMILES string
CCCCCCCCOCCl
InChI key
YUMNZEWYPUBSQA-UHFFFAOYSA-N
assay
95%
contains
0.1% 2,6-di-tert-butylphenol as stabilizer
refractive index
n20/D 1.437 (lit.)
density
0.924 g/mL at 25 °C (lit.)
functional group
chloro, ether
storage temp.
2-8°C
Quality Level
Related Categories
Application
Chloromethyl octyl ether has been employed as chloromethylation reagent:
- in chloromethylation of calix[4]arene, methyl ethers of calix[6]arene and calix[8]arene
- in the synthesis of chloromethylated poly(phthalazinone ether sulfone ketone)
- in chloromethylation of polyetherethersulphone-polyethersulphone copolymers
- for polymers
signalword
Warning
hcodes
Hazard Classifications
Carc. 2 - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
192.2 °F - closed cup
flash_point_c
89 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Journal of Polymer Science, 23, 231-231 (1985)
Chloromethylation of calixarenes and synthesis of new water soluble macrocyclic hosts.
Almi m, et al.
Tetrahedron, 45(7), 2177-2182 (1989)
Synthesis and characterization of quaternized poly (phthalazinone ether sulfone ketone) for anion-exchange membrane.
Jian XG, et al.
Chinese Chemical Letters = Zhongguo Hua Xue Kuai Bao, 18(10), 1269-1272 (2007)
Br. Polym. J., 16, 234-234 (1984)
On the chloromethylation of polyetherethersulphone/polyethersulphone copolymers. The use of triflic acid as catalyst.
Naik HA, et al.
Polymer, 33(1), 166-169 (1992)
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