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Merck
모든 사진(1)

주요 문서

87208

Supelco

Myristyltrimethylammonium bromide

suitable for ion pair chromatography, LiChropur, ≥99.0% (AT)

동의어(들):

Tetradecyltrimethylammonium bromide, Trimethyl(tetradecyl)ammonium bromide

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10 G
₩331,499

₩331,499


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10 G
₩331,499

About This Item

Linear Formula:
CH3(CH2)13N(Br)(CH3)3
CAS Number:
Molecular Weight:
336.39
Beilstein:
3633227
EC Number:
MDL number:
UNSPSC 코드:
12000000
PubChem Substance ID:
NACRES:
NB.21

₩331,499


구입 가능 여부는 고객센터에 문의하십시오.

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설명

cationic

Quality Level

분석

≥99.0% (AT)

양식

crystals

품질

LiChropur

분자량

micellar avg mol wt 27,000

응집 번호

80

기술

ion pair chromatography: suitable

CMC

4-5 mM (20-25°C)

mp

245-250 °C (lit.)

λ

10 % in H2O

UV 흡수

λ: 240 nm Amax: ≤0.08
λ: 250 nm Amax: ≤0.05
λ: 260 nm Amax: ≤0.04
λ: 500 nm Amax: ≤0.02

적합성

corresponds to standard for filter test

SMILES string

[Br-].CCCCCCCCCCCCCC[N+](C)(C)C

InChI

1S/C17H38N.BrH/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18(2,3)4;/h5-17H2,1-4H3;1H/q+1;/p-1

InChI key

CXRFDZFCGOPDTD-UHFFFAOYSA-M

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일반 설명

Ion-pairing reagents as mobile phase additives facilitate the separation of ionic and highly polar substances on reversed phase HPLC columns. Their purity is an important parameter for their successful application. Sigma-Aldrich offers an wide range of tailor-made reagents for anionic (quaternary ammonium and phosphonium salts) and cationic (alkanesulfonates) analyzes. All mobile phase additives are subject to rigorous testing with special emphasis on the requirements of modern reversed phase HPLC:

추천 제품

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

법적 정보

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Irrit. 2 - STOT RE 2 Oral - STOT SE 3

표적 기관

Gastrointestinal tract, Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

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


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이미 열람한 고객

Mohd Sajid Ali et al.
Journal of colloid and interface science, 352(2), 436-443 (2010-09-25)
Unfolding of rabbit serum albumin (RSA) by cationic surfactants cetyltrimethylammonium bromide (CTAB) and tetradecyltrimethylammonium bromide (TTAB) was studied by exploiting surface tensiometry, small-angle neutron scattering (SANS), intrinsic fluorescence, resonance Rayleigh scattering (RRS) (also referred as turbidity at 350/350), and circular
Juan Zhang et al.
The journal of physical chemistry. B, 114(41), 13128-13135 (2010-09-28)
Two fatty acids, perfluorononanoic acid (C(8)F(17)COOH) and nonanoic acid (C(8)H(17)COOH), were mixed with a cationic hydrocarbon surfactant, tetradecyltrimethylammonium hydroxide (TTAOH), in aqueous solutions for comparative investigation. Phase behaviors of the two systems are quite different because of the special properties
Suruchi Mahajan et al.
Langmuir : the ACS journal of surfaces and colloids, 28(50), 17238-17246 (2012-12-12)
Keeping in view the use of surfactants in drug delivery, the interactions of surface active ionic liquids, such as 1-tetradecyl-3-methylimidazolium bromide (C(14)mimBr), with drugs, viz., dopamine hydrochloride (DH) and acetylcholine chloride (AC), have been studied, and the results are further
Cexiong Fu et al.
Journal of chromatography. A, 1216(10), 1901-1907 (2009-02-03)
The usefulness of the micellar selectivity triangle (MST) for prediction and interpretation of separation patterns in micellar electrokinetic chromatography (MEKC) separations is presented. In addition, we demonstrate the capability of controlling selectivity properties of micelles through addition of organic modifiers
Changcheng Liu et al.
The journal of physical chemistry. B, 114(30), 9795-9804 (2010-07-14)
The phase behavior, rheological properties, and structures of two salt-free catanionic surfactant systems, tetradecyltrimethylammonium hydroxide ((TTA)OH)/lauric acid (LA)/H(2)O and cetyltrimethylammonium hydroxide ((CTA)OH)/LA/H(2)O, in the presence of deoxycholic acid (DeCA) were investigated and compared with the results of cholic acid (CA).

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