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161667

10-十一酰氯

Name: 10-十一酰氯
Brand: ALDRICH

97%

别名:

ψ-Undecenoyl chloride, ψ-Undecylenic acid chloride, 10-Hendecenoyl chloride, Undec-10-enoyl chloride

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关于此项目

线性分子式:

CH₂=CH(CH₂)₈COCl

化学文摘社编号:

38460-95-6

分子量:

202.72

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24849945

EC Number:

253-951-0

Beilstein/REAXYS Number:

1635112

MDL number:

MFCD00000772

Assay:

97%

Form:

liquid

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属性

Quality Level

100

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

说明

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).

pictograms

GHS05,GHS07

signalword

Danger

hcodes

H314,H335

pcodes

P280 - P303 + P361 + P353 - P305 + P351 + P338 + P310

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B - STOT SE 3

target_organs

Respiratory system

存储类别

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

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Olefin cross-metathesis as a source of polysaccharide derivatives: cellulose ω-carboxyalkanoates.

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

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)

Self-Assembly of Surface-Acylated Cellulose Nanowhiskers and Graphene Oxide for Multiresponsive Janus-Like Films with Time-Dependent Dry-State Structures.

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

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全球贸易项目编号

货号	GTIN
161667-100G	04061836698874
161667-25G	04061838346384