161667
10-Undecenoyl chloride
97%
Synonym(s):
ψ-Undecenoyl chloride, ψ-Undecylenic acid chloride, 10-Hendecenoyl chloride, Undec-10-enoyl chloride
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About This Item
Linear Formula:
CH2=CH(CH2)8COCl
CAS Number:
Molecular Weight:
202.72
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
253-951-0
Beilstein/REAXYS Number:
1635112
MDL number:
Assay:
97%
Form:
liquid
Quality Level
assay
97%
form
liquid
refractive index
n20/D 1.454 (lit.)
bp
120-122 °C/10 mmHg (lit.)
density
0.944 g/mL at 25 °C (lit.)
functional group
acyl chloride, allyl
SMILES string
ClC(=O)CCCCCCCCC=C
InChI
1S/C11H19ClO/c1-2-3-4-5-6-7-8-9-10-11(12)13/h2H,1,3-10H2
InChI key
MZFGYVZYLMNXGL-UHFFFAOYSA-N
Application
10-Undecenoyl chloride was used as acylating reagent in the synthesis of cellulose ω-carboxyalkanoates and poly(ethylene glycol)–lipid amphiphiles. It was used in synthesis and modification of hyperbranched poly(glycidol).
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
target_organs
Respiratory system
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
199.4 °F
flash_point_c
93 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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Huan Liu et al.
Small (Weinheim an der Bergstrasse, Germany), 16(44), e2004922-e2004922 (2020-10-09)
For the first time Janus-like films of surface-acylated cellulose nanowhiskers (CNWs) with or without graphene oxide (GO) via one-step evaporation-driven self-assembly process are reported, which have reconstructible time-dependent micro-/nanostructures and asymmetric wettability. The heterogeneous aggregation of CNWs on rough Teflon
Enhancement of the impact strength of cationically cured cycloaliphatic diepoxide by adding hyperbranched poly (glycidol) partially modified with 10-undecenoyl chains.
Flores M, et al.
Eur. Polymer J., 49(6), 1610-1620 (2013)
Xiangtao Meng et al.
Biomacromolecules, 15(1), 177-187 (2013-12-18)
Cross-metathesis has been shown for the first time to be a useful method for the synthesis of polysaccharide derivatives, focusing herein on preparation of cellulose ω-carboxyalkanoates. Commercially available cellulose esters were first acylated with 10-undecenoyl chloride, providing esters with olefin-terminated
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 161667-100G | 04061836698874 |
| 161667-25G | 04061838346384 |