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安全性情報

722987

Sigma-Aldrich

2-シアノ-2-プロピルベンゾジチオエート

>97% (HPLC)

別名:

2-シアノ-2-イルベンゾジチオエート

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About This Item

実験式（ヒル表記法）:
C11H11NS2
CAS番号:
201611-85-0
分子量:
221.34
MDL番号:
MFCD09037881
UNSPSCコード:
12352100
PubChem Substance ID:
329763965
NACRES:
NA.23

アッセイ

>97% (HPLC)

形状

solid or liquid

屈折率

n20/D 1.621

mp

28-31 °C

密度

1.146 g/mL at 25 °C

保管温度

2-8°C

SMILES記法

CC(C)(SC(=S)c1ccccc1)C#N

InChI

1S/C11H11NS2/c1-11(2,8-12)14-10(13)9-6-4-3-5-7-9/h3-7H,1-2H3

InChI Key

IDSLBLWCPSAZBL-UHFFFAOYSA-N

関連するカテゴリー

詳細

適切なRAFT剤の選択にお困りですか。モノマーに対するRAFT剤compatibility tableをご覧ください。

アプリケーション

可逆的付加開裂連鎖移動（RAFT）重合
制御ラジカル重合のRAFT剤；特にメタクリレート（メタクリル酸塩）およびメタクリルアミドモノマーの重合に適しています。 連鎖移動剤（CTA）

ピクトグラム

Exclamation mark
GHS07

シグナルワード

Warning

危険有害性情報

H317

危険有害性の分類

Skin Sens. 1

保管分類コード

10 - Combustible liquids

WGK

WGK 3

引火点(°F)

>230.0 °F - closed cup

引火点(℃)

> 110 °C - closed cup

適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

毒物及び劇物取締法

劇物

Jan Code

722987-5G:4548173299563
722987-VAR:
722987-BULK:
722987-1G:4548173299556

最新バージョンのいずれかを選択してください：

試験成績書（COA）

Lot/Batch Number
MKCP5045
MKCN2568
MKCM5874
MKCL7228
MKCM0323

適切なバージョンが見つかりませんか。

特定のバージョンが必要な場合は、ロット番号またはバッチ番号で特定の証明書を検索できます。

COAを検索

以前この製品を購入いただいたことがある場合

文書ライブラリで、最近購入した製品の文書を検索できます。

文書ライブラリにアクセスする

Laura Marcela Forero Ramirez et al.
Carbohydrate polymers, 224, 115153-115153 (2019-09-02)
A multi-reactive polysaccharide-based transurf (acting both as macro-Chain Transfer Agent and stabilizer) was used to confine RAFT polymerization of methyl methacrylate (MMA) at the oil/water (o/w) miniemulsion interface. Dithiobenzoate groups and hydrophobic aliphatic side chains were introduced onto dextran, conferring
Katharina Nieswandt et al.
Materials (Basel, Switzerland), 12(19) (2019-09-29)
In this work, we present a novel synthetic route to diblock copolymers based on styrene and 3-vinylpyridine monomers. Surfactant-free water-based reversible addition-fragmentation chain transfer (RAFT) emulsion polymerization of styrene in the presence of the macroRAFT agent poly(3-vinylpyridine) (P3VP) is used
Xiaohan Zhang et al.
Langmuir : the ACS journal of surfaces and colloids, 34(27), 7998-8006 (2018-06-28)
Amphiphilic poly( N-(2-hydroxypropyl)methacrylamide) copolymers ( pHPMA) bearing cholesterol side groups in phosphate buffer saline self-assemble into nanoparticles (NPs) which can be used as tumor-targeted drug carriers. It was previously shown by us that human serum albumin (HSA) interacts weakly with
Ryuichi Nakatani et al.
ACS applied materials & interfaces, 9(37), 31266-31278 (2017-03-18)
In this study, a series of perpendicular lamellae-forming poly(polyhedral oligomeric silsesquioxane methacrylate-block-2,2,2-trifluoroethyl methacrylate)s (PMAPOSS-b-PTFEMAs) was developed based on the bottom-up concept of creating a simple yet effective material by tailoring the chemical properties and molecular composition of the material. The
Laure Gevaux et al.
Polymers, 11(2) (2019-04-10)
Fouling Release Coatings are marine antifouling coatings based on silicone elastomers. Contrary to commonly used biocide-based antifouling coatings, they do not release biocides into the marine environment, however, they suffer from poor antifouling efficacy during idle periods. To improve their
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資料

Evaluation of RAFT Agents

Evaluation of RAFT Agents

Evaluation of RAFT Agents

A series of polymerization were carried out using RAFT agents and monomers yielding well-defined polymers with narrow molecular weight distributions. The process allows radical-initiated growing polymer chains to degeneratively transfer reactivity from one to another through the use of key functional groups (dithioesters, trithiocarbonates, xanthates and dithiocarbamates). RAFT agents help to minimize out-of-control growth and prevent unwanted termination events from occurring, effectively controlling polymer properties like molecular weight and polydispersity. RAFT agents are commercially available. RAFT does not use any cytotoxic heavy metal components (unlike ATRP).

Reversible Addition Fragmentation Chain Transfer (RAFT) Polymerization

RAFT (Reversible Addition Fragmentation chain Transfer) polymerization is a reversible deactivation radical polymerization (RDRP) and one of the more versatile methods for providing living characteristics to radical polymerization.

Reversible Addition Fragmentation Chain Transfer (RAFT) Polymerization

RAFT (Reversible Addition Fragmentation chain Transfer) polymerization is a reversible deactivation radical polymerization (RDRP) and one of the more versatile methods for providing living characteristics to radical polymerization.

すべて表示

プロトコル

RAFT Polymerization Procedures

RAFT (Reversible Addition-Fragmentation chain Transfer) is a form of living radical polymerization involving conventional free radical polymerization of a substituted monomer in the presence of a suitable chain transfer (RAFT) reagent.

Concepts and Tools for RAFT Polymerization

Sigma-Aldrich presents an article about RAFT, or Reversible Addition/Fragmentation Chain Transfer, which is a form of living radical polymerization.

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