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Merck
모든 사진(1)

주요 문서

251194

Sigma-Aldrich

1-Fluoropentane

98%

동의어(들):

Amyl fluoride

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About This Item

Linear Formula:
CH3(CH2)4F
CAS Number:
Molecular Weight:
90.14
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

분석

98%

양식

liquid

refractive index

n20/D 1.36 (lit.)

bp

62-63 °C (lit.)

density

0.789 g/mL at 25 °C (lit.)

작용기

alkyl halide
fluoro

SMILES string

CCCCCF

InChI

1S/C5H11F/c1-2-3-4-5-6/h2-5H2,1H3

InChI key

OEPRBXUJOQLYID-UHFFFAOYSA-N

일반 설명

Dual luminescence of 4-N,N-dimethylaminobenzonitrile has been observed in 1-fluoropentane.

애플리케이션

1-Fluoropentane has been used in the synthesis of 6-F-B10H13 and 6-Cl- B10H13 (halodecaboranes).

픽토그램

FlameExclamation mark

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

표적 기관

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point (°F)

-9.4 °F - closed cup

Flash Point (°C)

-23 °C - closed cup

개인 보호 장비

Eyeshields, Faceshields, Gloves


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시험 성적서(COA)

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문서 라이브러리 방문

이미 열람한 고객

K R Harikumar et al.
Nature chemistry, 1(9), 716-721 (2010-12-03)
The controlled imprinting of surfaces with specified patterns is important in the development of nanoscale devices. Previously, such patterns were created using self-assembled physisorbed adsorbate molecules that can be stabilized on the surface by subsequent chemical bonding. Here we show
C F Nhachi et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 26(8), 705-713 (1988-08-01)
Phenobarbitone pretreatment potentiated hepatocyte lesions in male rats 24 hr after treatment with 1-fluoropentane (3.5 mg/kg body weight) and 1-fluorohexane (0.17 mg/kg body weight). Serum levels of the enzymes ornithine carbamyltransferase, glutamic-pyruvic transaminase and gamma-glutamyltranspeptidase were significantly elevated by the
William C Ewing et al.
Inorganic chemistry, 47(19), 8580-8582 (2008-08-30)
The high-yield syntheses of 6-X-B 10H 13 [X = Cl (88%), Br (96%), I (84%)] resulted from the cage-opening reactions of the (NH 4 (+)) 2B 10H 10 (2-) salt with ionic-liquid-based superacidic hydrogen halides, while both the previously unknown
The role of the solvent in the dual luminescence of 4-N, N-dimethylaminobenzonitrile.
Suppan P.
Chemical Physics Letters, 128(2), 160-161 (1986)

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