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Merck
모든 사진(1)

문서

394467

Sigma-Aldrich

Morpholine

purified by redistillation, ≥99.5%

동의어(들):

Tetrahydro-1,4-oxazine

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About This Item

실험식(Hill 표기법):
C4H9NO
CAS Number:
Molecular Weight:
87.12
Beilstein:
102549
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor density

3 (vs air)

vapor pressure

31 mmHg ( 38 °C)
7 mmHg ( 20 °C)

분석

≥99.5%

형태

liquid

autoignition temp.

590 °F

정제법

redistillation

expl. lim.

10.8 %

refractive index

n20/D 1.454 (lit.)

bp

129 °C (lit.)
129 °C

mp

−7-−5 °C (lit.)

solubility

water: miscible

density

0.996 g/mL at 25 °C (lit.)

SMILES string

C1COCCN1

InChI

1S/C4H9NO/c1-3-6-4-2-5-1/h5H,1-4H2

InChI key

YNAVUWVOSKDBBP-UHFFFAOYSA-N

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관련 카테고리

일반 설명

Morpholine is a heterocyclic secondary amine. It is formed by the condensation of diethanolamine and sulfuric acid. Its IR spectra and Raman spectra at -180°C has been recorded. The crystal structure of morpholine has been determined at 150K. The microwave spectra of morpholine within the 8 to 40GHz region have been investigated. Ascorbate anion and glutathione have been reported to inhibit the aqueous reaction between nitrogen dioxide and morpholine. Conformational studies by Raman spectroscopy and theoretical calculations suggest that equatorial chair conformation of morpholine predominates in the pure liquid state. Degradation of morpholine using Mycobacterium sp. strain RP1 has been proposed.

애플리케이션

Morpholine is suitable for use as a test compound in the study of morpholine biodegradation by Mycobacterium strains.
It may be used in the following studies:
  • As a reactant in the synthesis of 1,3-dihydro-1-hydroxy-3-morpholin-4-yl-2,1-benzoxaborole by reacting with o-formylphenylboronic acid.
  • As a corrosion inhibitor and to maintain basic pH in boiler feed water.
  • As a reactant in the bis(β-ketoenolates)nickel(II) adducts of morpholine.
  • As one of the reagent used in the colorimetric quantitative determination of C-2 unsubstituted phenothiazine derivatives.
  • As a reactant in the quantitative determination of α,β-unsaturated compounds.

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Repr. 2 - Skin Corr. 1B

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point (°F)

87.8 °F - closed cup

Flash Point (°C)

31 °C - closed cup

개인 보호 장비

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


시험 성적서(COA)

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문서 라이브러리 방문

이미 열람한 고객

P Poupin et al.
Applied and environmental microbiology, 64(1), 159-165 (1998-01-22)
A Mycobacterium strain (RP1) was isolated from a contaminated activated sludge collected in a wastewater treatment unit of a chemical plant. It was capable of utilizing morpholine and other heterocyclic compounds, such as pyrrolidine and piperidine, as the sole source
S R el-Shabouri et al.
Journal - Association of Official Analytical Chemists, 69(5), 821-824 (1986-09-01)
A colorimetric method for quantitative determination of 6 C-2 unsubstituted phenothiazine derivatives is described. The method is based on reaction of phenothiazine derivative with morpholine and N-bromosuccinimide reagents in aqueous methanol at 60 degrees C to produce a blue color.
Adducts of Piperidine, Piperazine, Methylpiperazine, and Morpholine with Bis (β-Ketoenolates) of Nickel (II).
Marcotrigiano G,et al.
Canadian Journal of Chemistry, 50(16), 2557-2560 (1972)
Microwave spectrum of morpholine.
Sloan JJ and Kewley R.
Canadian Journal of Chemistry, 47(18), 3453-3462 (1969)
Determination of Alpha, Beta-Unsaturated Compouds by Reaction with Morpholine
Critchfield FE, et al.
Analytical Chemistry, 28(1), 76-79 (1956)

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