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Merck
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04500

Sigma-Aldrich

N-乙基吗啉

≥97.0% (GC)

别名:

N-Ethylmorpholine

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About This Item

经验公式（希尔记法）:
C6H13NO
CAS号:
100-74-3
分子量:
115.17
Beilstein:
102969
EC號碼:
202-885-0
MDL號碼:
MFCD00006177
分類程式碼代碼:
12352100
eCl@ss:
39162412
PubChem物質ID:
329747936
NACRES:
NA.22

品質等級

100

化驗

≥97.0% (GC)

雜質

≤3% 4-methylmorpholine

折射率

n20/D 1.441 (lit.)
n20/D 1.442

bp

139 °C (lit.)

mp

−63 °C (lit.)

密度

0.91 g/mL at 20 °C (lit.)

官能基

ether

SMILES 字串

CCN1CCOCC1

InChI

1S/C6H13NO/c1-2-7-3-5-8-6-4-7/h2-6H2,1H3

InChI 密鑰

HVCNXQOWACZAFN-UHFFFAOYSA-N

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相关类别

訊號詞

Danger

危險分類

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

儲存類別代碼

3 - Flammable liquids

水污染物質分類（WGK）

WGK 1

閃點（°F）

86.0 °F - closed cup

閃點（°C）

30 °C - closed cup

個人防護裝備

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

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分析证书(COA)

Lot/Batch Number
BCCG7757
BCCD7039
BCCC0308

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Andreas Zettl et al.
The American journal of pathology, 161(5), 1635-1645 (2002-11-05)
Genetic alterations in enteropathy-type T-cell lymphoma (ETL) are unknown so far. In this series, 38 cases of ETL were analyzed by comparative genomic hybridization (CGH). CGH revealed chromosomal imbalances in 87% of cases analyzed, with recurrent gains of genetic material
Manja Newe et al.
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Skin fibrosis is a complex biological remodeling process occurring in disease like systemic sclerosis, morphea, or eosinophilic fasciitis. Since the knowledge about the underlying pathomechanisms is still incomplete, there is currently no therapy, which prevents or reverses skin fibrosis sufficiently.
V S Kamanna et al.
Biochimica et biophysica acta, 1043(1), 119-121 (1990-03-12)
Apolipoprotein B (ApoB) in general is known as an insoluble protein in aqueous buffers without the initial aid of denaturing agents. However, following the total delipidization of rat plasma low-density lipoproteins, a considerable portion (28.2 +/- 3.0%) of rat ApoB
Jesús Muñoz-Estrada et al.
Journal of cell science, 132(17) (2019-08-09)
Mutations in the Abelson-helper integration site 1 (AHI1) gene are associated with neurological/neuropsychiatric disorders, and cause the neurodevelopmental ciliopathy Joubert syndrome (JBTS). Here, we show that deletion of the transition zone (TZ) protein Ahi1 in mouse embryonic fibroblasts (MEFs) has
Seh-Jin Yang et al.
Organic letters, 11(15), 3438-3441 (2009-07-09)
A new, nondestructive, highly sensitive method for colorimetric monitoring of primary amines, secondary amines, and thiols on a solid support was developed. The resin used in this method is simply regenerated for the repetition of the reaction or an ensuing
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