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Merck
모든 사진(2)

주요 문서

50053

Sigma-Aldrich

Glycidyltrimethylammonium chloride

technical, ≥90% (calc. based on dry substance, AT)

동의어(들):

(2,3-Epoxypropyl)trimethylammonium chloride

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About This Item

실험식(Hill 표기법):
C6H14ClNO
CAS Number:
Molecular Weight:
151.63
Beilstein:
3914931
MDL number:
UNSPSC 코드:
12352302
PubChem Substance ID:
NACRES:
NA.22

grade

technical

Quality Level

분석

≥90% (calc. based on dry substance, AT)

불순물

2-4% chlorohydrin
20-25% water

density

1.13 g/mL at 20 °C (lit.)

저장 온도

2-8°C

SMILES string

[Cl-].C[N+](C)(C)CC1CO1

InChI

1S/C6H14NO.ClH/c1-7(2,3)4-6-5-8-6;/h6H,4-5H2,1-3H3;1H/q+1;/p-1

InChI key

PUVAFTRIIUSGLK-UHFFFAOYSA-M

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일반 설명

Glycidyltrimethylammonium chloride (GTMAC) is a cationizing agent commonly used for starch modification.

애플리케이션

Glycidyltrimethylammonium chloride be used as a derivatizing agent to synthesize N-(2-hydroxypropyl)-3-trimethylammonium chitosan chloride (HTCC), a water-soluble chitosan derivative, by reacting with chitosan. HTCC can form nanocomposite films with silver nanoparticles that show good antimicrobial property and optical transparency. Cationic starches can also be prepared by derivatization of starch with GTMAC.

주의사항

hydrolysis on storage (approx. 3.5%/month at 20°C)

관련 제품

제품 번호
설명
가격

픽토그램

Health hazardCorrosionExclamation mark

신호어

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 1B - Eye Dam. 1 - Muta. 2 - Repr. 1B - Skin Sens. 1 - STOT RE 2 - STOT SE 2

표적 기관

Kidney

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point (°F)

338.0 °F - closed cup

Flash Point (°C)

170 °C - closed cup

개인 보호 장비

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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문서 라이브러리 방문

Le Thi Tuyet Nhung et al.
Polymers, 12(11) (2020-11-21)
An efficient and effective process for the production of high-performance anion exchange membranes (AEMs) is necessary for the commercial application of fuel cells. Therefore, in this study, quaternized poly vinylbenzyl chloride (QVBC) and polysulfone were composited with glycidyltrimethylammonium-chloride-quaternized chitosan (QCS)
Wai Yan Cheah et al.
International journal of biological macromolecules, 126, 569-577 (2018-12-26)
The electrospinning PAN nanofiber membrane (P-CN) was hydrolysed to convert carboxylic groups as reaction sites and covalently graft chitosan molecule. The chitosan derivatives with quaternary ammonium groups exerted greater efficiency against bacteria as compared to pure chitosan. Hence, the chitosan
E Pedone et al.
Journal of controlled release : official journal of the Controlled Release Society, 77(1-2), 139-153 (2001-11-02)
Hydrophilic polycations form complexes when mixed with plasmids. Following functionalisation with glycidyltrimethylammonium chloride (GTA) alpha,beta-poly(asparthylhydrazide) (PAHy), a water-soluble synthetic macromolecule, becomes polycationic and potentially useful for systemic gene delivery. Initially the biocompatibility of PAHy and PAHy-GTA derivatives with different degrees
Sirlei Rosa et al.
Journal of hazardous materials, 155(1-2), 253-260 (2008-01-09)
Adsorption of reactive orange 16 by quaternary chitosan salt (QCS) was used as a model to demonstrate the removal of reactive dyes from textile effluents. The polymer was characterized by infrared (IR), energy dispersive X-ray spectrometry (EDXS) analyses and amount
Shingo Sotoma et al.
Materials (Basel, Switzerland), 11(8) (2018-08-22)
Cationic polymers are often employed in conjugation with nanomaterials, and the resultant hybrids are useful for various bioapplications. Here, a single-step metal-free method for the synthesis of fluorescent nanodiamonds (FNDs) conjugated with cationic polymer brushes is reported. Distinct from the

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