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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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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

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)

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

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全球贸易项目编号

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