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Merck
CN

442700

十五烷

analytical standard

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线性分子式:
CH3(CH2)13CH3
化学文摘社编号:
分子量:
212.41
EC Number:
211-098-1
UNSPSC Code:
41121813
PubChem Substance ID:
Beilstein/REAXYS Number:
1698194
MDL number:
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InChI key

YCOZIPAWZNQLMR-UHFFFAOYSA-N

InChI

1S/C15H32/c1-3-5-7-9-11-13-15-14-12-10-8-6-4-2/h3-15H2,1-2H3

SMILES string

CCCCCCCCCCCCCCC

grade

analytical standard

vapor density

7.4 (vs air)

vapor pressure

1 mmHg ( 91.6 °C)

description

This product has been discontinued. It has been replaced by product 76509.

expl. lim.

6.5 %

packaging

ampule of 1000 mg

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

refractive index

n20/D 1.431 (lit.)

bp

270 °C (lit.)

mp

8-10 °C (lit.)

density

0.769 g/mL at 25 °C (lit.)

application(s)

environmental
petroleum

format

neat

storage temp.

room temp

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Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

pictograms

Health hazard

signalword

Danger

hcodes

Hazard Classifications

Asp. Tox. 1

supp_hazards

存储类别

10 - Combustible liquids

wgk

WGK 1

flash_point_f

219.2 °F - closed cup

flash_point_c

104 °C - closed cup

ppe

Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Keith D Schwartz et al.
Organic letters, 13(2), 248-251 (2010-12-18)
Conjugate reduction of an enone accompanied by in situ intramolecular aldol condensation was used to construct the tetrasubstituted cyclohexane nucleus of phomactins. Subsequent relay ring-closing metathesis completed the nine-membered ansa bridge of the diterpenoid framework.
From 2,2'-methylenedifuran to all stereomeric pentadecane-1,3,5,7,9,11,13,15-octols.
M E Schwenter et al.
The Journal of organic chemistry, 66(23), 7869-7872 (2001-11-10)
Biosynthesis of phomactins: common intermediate phomactatriene and taxadiene.
Tetsuo Tokiwano et al.
Chemical communications (Cambridge, England), (11)(11), 1324-1325 (2004-05-22)
Nao Fujiwara-Tsujii et al.
Zoological science, 23(4), 353-358 (2006-05-17)
The alarm pheromone of the ant Camponotus obscuripes (Formicinae) was identified and quantified by gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS). Comparisons between alarm pheromone components and extracts from the major exocrine gland of this ant species revealed that
Synthesis of homogeneous FePt nanoparticles using a nitrile ligand.
Virginie Monnier et al.
Small (Weinheim an der Bergstrasse, Germany), 4(8), 1139-1142 (2008-07-16)

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