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H28807

Sigma-Aldrich

1-(2-Hydroxyethyl)piperazine

98%

Synonym(s):

2-Piperazinoethanol, Piperazine-1-ethanol

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About This Item

Empirical Formula (Hill Notation):
C6H14N2O
CAS Number:
103-76-4
Molecular Weight:
130.19
Beilstein:
104361
EC Number:
203-142-3
MDL number:
MFCD00005970
UNSPSC Code:
12352100
PubChem Substance ID:
24895538
NACRES:
NA.22

Assay

98%

refractive index

n20/D 1.506 (lit.)

bp

246 °C (lit.)

density

1.061 g/mL at 25 °C (lit.)

SMILES string

OCCN1CCNCC1

InChI

1S/C6H14N2O/c9-6-5-8-3-1-7-2-4-8/h7,9H,1-6H2

InChI key

WFCSWCVEJLETKA-UHFFFAOYSA-N

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Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H315,H318

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 1

Flash Point(F)

275.0 °F

Flash Point(C)

135 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Ana I Loureiro et al.
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Patrice N Mimche et al.
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William H Parker et al.
Biochemical and biophysical research communications, 458(2), 262-267 (2015-02-04)
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Katalin F Medzihradszky et al.
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Beam-type collision-induced dissociation (CID) data of intact glycopeptides isolated from mouse liver tissue are presented to illustrate characteristic fragmentation of differentially sialylated glycopeptides. Eight glycoforms of an O-linked glycopeptide from Nucleobindin-1 are distinguished on the basis of the precursor masses
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