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Merck

394912

Supelco

ヘプタフルオロ酪酸無水物

for GC derivatization, LiChropur, ≥99.0%

別名:

HFBA, HFAA, パーフルオロ酪酸無水物

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About This Item

化学式:
(CF3CF2CF2CO)2O
CAS番号:
分子量:
410.06
Beilstein:
856036
EC Number:
MDL番号:
UNSPSCコード:
12000000
PubChem Substance ID:
NACRES:
NA.22

グレード

derivatization grade ((GC derivatization))
for GC derivatization

アッセイ

≥99.0%

フォーム

liquid

品質

LiChropur

反応適合性

reagent type: derivatization reagent
reaction type: Acylations

テクニック

gas chromatography (GC): suitable

屈折率

n20/D 1.287 (lit.)

bp

108-110 °C (lit.)

mp

−43 °C (lit.)

密度

1.674 g/mL at 20 °C (lit.)

SMILES記法

FC(F)(F)C(F)(F)C(F)(F)C(=O)OC(=O)C(F)(F)C(F)(F)C(F)(F)F

InChI

1S/C8F14O3/c9-3(10,5(13,14)7(17,18)19)1(23)25-2(24)4(11,12)6(15,16)8(20,21)22

InChI Key

UFFSXJKVKBQEHC-UHFFFAOYSA-N

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詳細

Heptafluorobutyric anhydride (HFB) is a derivatizing reagent. It provides facile and sensitive way for detecting and elucidating structure of numerous alkyl-chain homologs.

アプリケーション

Learn more in the Product Information
GC derivatizing agent used to prepare volatile derivatives of amino acids and other biologically active compounds.
HFB was used as derivatizing agent in analysing platelet-activating factor using GC-MS.
Suitable for the derivatization of aldosterone, digoxin, digitoxin and metabolites, estradiol, postaglandins F and F2α, 3-oxo-Δ4-steroids, and testosterone.

包装

Derivatization reagent used in a GC-MS analysis of stereoisomer content of synthetic peptides.

その他情報

Reagent for heptafluorobutyrate, 3-enol heptafluorobutyrate, 17-heptafluorobutyrate, heptafluorobutyrate and heptafluorobutyryl.

法的情報

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

ピクトグラム

Corrosion

シグナルワード

Danger

危険有害性情報

危険有害性の分類

Skin Corr. 1B

保管分類コード

8A - Combustible corrosive hazardous materials

WGK

WGK 3

引火点(°F)

Not applicable

引火点(℃)

Not applicable

個人用保護具 (PPE)

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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。

Jan Code

394912-VAR:
394912-10ML:
394912-20ML:
394912-BULK:
394912-1ML:
394912-25ML:
394912-100ML:
394912-5ML:
394912-10X1ML:


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試験成績書(COA)

Lot/Batch Number

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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

S T Weintraub et al.
Journal of lipid research, 31(4), 719-725 (1990-04-01)
Parallel analysis of platelet-activating factor (PAF) using chemical ionization gas chromatography-mass spectrometry after direct derivatization with pentafluorobenzoyl chloride (PFB) and heptafluorobutyric anhydride (HFB) provides a facile and highly sensitive means for detecting and elucidating the structure of the numerous alkyl-chain
J Bakthavachalam et al.
Journal of chromatography, 500, 373-386 (1990-02-02)
Several electrophoric derivatives of 1-aminopyrene and 2-aminofluorene were prepared. Reagents such as heptafluorobutyryl chloride, pentafluorobenzoyl chloride, pentafluorobenzyl bromide and pentafluorobenzaldehyde, alone and in certain combinations, were employed. The ease of formation, yield, stability and fragmentation by gas chromatography with electron-capture
Ralf Pätzold et al.
Chirality, 18(7), 551-557 (2006-05-10)
Synthetic dipeptides comprising mixtures of enantiomers, diastereomers, or sequential isomers were converted into their N-perfluoroacetyl dipeptide esters (perfluoroacetyl: trifluoroacetyl, pentafluoroacetyl, heptafluorobutyryl; ester: methyl, 1-propyl, 2-propyl, 2,2,2-trifluoroethyl) and analyzed by GC-MS on the chiral stationary phases Chirasil-L-Val and Lipodex-E using helium
C Fakt et al.
Journal of chromatography. B, Biomedical sciences and applications, 700(1-2), 93-100 (1997-12-09)
A convenient and sensitive method for the quantitative determination of poly(ethylene glycol) 400 in plasma and urine with capillary gas chromatography-mass spectrometry has been developed. The sample preparation involves solid-phase extraction with subsequent derivatization with heptafluorobutyric anhydride, which proved to
Oliver Lerch et al.
Journal of chromatography. A, 991(1), 77-97 (2003-04-22)
Methods for ultra trace detection of endocrine disruptive chemicals (EDCs) are needed because of their low levels of impact. Twenty-one EDCs were selected, including 17beta-estradiol, 17alpha-ethinylestradiol, 17beta-testosterone and bisphenol A. Derivatisation with eight different fluorine containing compounds was examined. All

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