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Merck
모든 사진(1)

주요 문서

415693

Sigma-Aldrich

8-Chloro-1-octanol

98%

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크기 선택

25 ML
₩187,572

₩187,572


출고 가능일2025년 4월 21일세부사항


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보기 변경
25 ML
₩187,572

About This Item

Linear Formula:
Cl(CH2)8OH
CAS Number:
Molecular Weight:
164.67
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

₩187,572


출고 가능일2025년 4월 21일세부사항


벌크 견적 요청

Quality Level

분석

98%

refractive index

n20/D 1.458 (lit.)

bp

129-130 °C/11 mmHg (lit.)

density

0.976 g/mL at 25 °C (lit.)

작용기

chloro
hydroxyl

SMILES string

OCCCCCCCCCl

InChI

1S/C8H17ClO/c9-7-5-3-1-2-4-6-8-10/h10H,1-8H2

InChI key

YDFAJMDFCCJZSI-UHFFFAOYSA-N

일반 설명

8-Chloro-1-octanol is a ω-chloro-1-alkanol.[1]

애플리케이션

8-Chloro-1-octanol may be employed for the following studies:
  • Biosynthesis of bacteriochlorophyll c derivatives, via esterification.[1]
  • Preparation of new macroporous triisobutylphosphine sulphide functionalized polymers.[2]
  • Synthesis of series of new mesogenic azomethine diols.[3]
  • Synthesis of bis(4-hydroxyoctoxyphenyl)sulfone (HOS).[4]

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

Eyeshields, Gloves


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문서 라이브러리에서 최근에 구매한 제품에 대한 문서를 찾아보세요.

문서 라이브러리 방문

New macroporous polymers for the selective adsorption of gold (III) and palladium (II). I. The synthesis, characterization, and effect of spacers on metal adsorption.
Sanchez JM, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 38(2), 269-278 (2000)
Issam Ahmed Mohammed et al.
Molecules (Basel, Switzerland), 15(5), 3260-3269 (2010-07-27)
A series of new mesogenic azomethine diols were successfully synthesized by condensation reactions between various chloroalkanols and N,N'-bis(4-hydroxy)-benzylidene-o-toluidine (1). The structures of these compounds were confirmed by CHN, FT-IR, (1)H-NMR, and (13)C-NMR spectrophotometer. Their thermotropic liquid crystalline behavior was studied
Synthesis and Properties of a Ferrocene-based Metallomesogenic Polymer Containing Bis (4-hydroxyoctoxyphenyl) sulfone.
Amer WA, et al.
Journal of Inorganic and Organometallic Polymers and Materials, 22(6), 1229-1239 (2012)
Yoshitaka Saga et al.
Journal of bioscience and bioengineering, 118(1), 82-87 (2014-02-06)
The green sulfur photosynthetic bacterium Chlorobaculum tepidum newly produced BChl c derivatives possessing a chlorine or bromine atom at the terminus of the esterifying chain in the 17-propionate residue by cultivation with exogenous ω-halo-1-alkanols. The relative ratios of BChl c
Zachary K Zander et al.
Biomaterials, 178, 339-350 (2018-05-23)
The use of catheters is ubiquitous in medicine and the incidence of infection remains unacceptably high despite numerous advances in functional surfaces and drug elution. Herein we report the use of a thermoplastic polyurethane containing an allyl ether side-chain functionality

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