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Merck
CN

74989

辛胺

analytical standard

别名:

1-氨基辛烷, 正辛胺, 辛基胺

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关于此项目

线性分子式:
CH3(CH2)7NH2
化学文摘社编号:
分子量:
129.24
EC Number:
203-916-0
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
1679227
MDL number:
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grade

analytical standard

Quality Level

vapor pressure

1 mmHg ( 20 °C)

assay

≥99.5% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

impurities

≤0.2% water

refractive index

n20/D 1.429

bp

175-177 °C (lit.)

mp

−5-−1 °C (lit.)

density

0.782 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

SMILES string

CCCCCCCCN

InChI

1S/C8H19N/c1-2-3-4-5-6-7-8-9/h2-9H2,1H3

InChI key

IOQPZZOEVPZRBK-UHFFFAOYSA-N

Application

Octylamine may be used as an ion pairing reagent for the separation and determination of biogenic amines and precursor aminoacids in various food samples using ion-pair high-performance liquid chromatography technique.
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.


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wgk

WGK 3

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Aquatic Acute 1 - Aquatic Chronic 2 - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A - STOT SE 3

target_organs

Respiratory system

存储类别

3 - Flammable liquids

flash_point_f

140.0 °F - closed cup

flash_point_c

60 °C - closed cup

ppe

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

法规信息

危险化学品

此项目有



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Ion-pair HPLC determination of biogenic amines and precursor aminoacids. Application of a method based on simultaneous use of heptanesulphonate and octylamine to some foods
Arlorio.M, et al.
Chromatographia, 48(11-12), 763-769 (1998)
Kristine Spildo et al.
Journal of colloid and interface science, 252(2), 470-472 (2005-11-18)
The adsorption of octanoic acid (Octac) and octylamine (Octam) onto silica from isooctane solutions has been studied, both from individual solutions of Octac and Octam and from mixtures of the two in isooctane. The results show that Octam has a
Erin Harleton et al.
The Journal of pharmacology and experimental therapeutics, 310(3), 1011-1019 (2004-05-04)
The anticancer drug N,N,"N"-triethylenethiophosphoramide (tTEPA) inactivated CYP2B6 and CYP2B1 in the reconstituted system in a time-, concentration-, and NADPH-dependent manner indicative of mechanism-based inactivation. The KI value for the inactivation of CYP2B1 was 38 microM, the kinact was 0.3 min(-1)



全球贸易项目编号

货号GTIN
74989-1ML04061832897752