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80621

Sigma-Aldrich

Piperazine

BioUltra, anhydrous, ≥99.0% (T)

Sinonimo/i:

1,4-Diazacyclohexane, Diethylenediamine

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About This Item

Formula empirica (notazione di Hill):
C4H10N2
Numero CAS:
110-85-0
Peso molecolare:
86.14
Beilstein:
102555
Numero CE:
203-808-3
Numero MDL:
MFCD00005953
Codice UNSPSC:
12161700
eCl@ss:
39160301
ID PubChem:
329769002
NACRES:
NA.25

Tensione di vapore

0.8 mmHg ( 20 °C)

Livello qualitativo

200

Nome Commerciale

BioUltra

Saggio

≥99.0% (T)

Forma fisica

solid

Limite di esplosione

14 %

Impurezze

insoluble matter, passes filter test
≤1% water

pH

11.0-12.5 (25 °C, 0.1 M in H2O)

P. eboll.

145-146 °C (lit.)

Punto di fusione

109-112 °C (lit.)

Solubilità

H2O: 0.1 M at 20 °C, clear, colorless

Anioni in tracce

chloride (Cl-): ≤50 mg/kg
sulfate (SO42-): ≤50 mg/kg

Cationi in tracce

Al: ≤5 mg/kg
As: ≤0.1 mg/kg
Ba: ≤5 mg/kg
Bi: ≤5 mg/kg
Ca: ≤10 mg/kg
Cd: ≤5 mg/kg
Co: ≤5 mg/kg
Cr: ≤5 mg/kg
Cu: ≤5 mg/kg
Fe: ≤5 mg/kg
K: ≤50 mg/kg
Li: ≤5 mg/kg
Mg: ≤5 mg/kg
Mn: ≤5 mg/kg
Mo: ≤5 mg/kg
Na: ≤50 mg/kg
Ni: ≤5 mg/kg
Pb: ≤5 mg/kg
Sr: ≤5 mg/kg
Zn: ≤5 mg/kg

λ

0.1 M in H2O

Assorbanza UV

λ: 260 nm Amax: 0.035
λ: 280 nm Amax: 0.010

Stringa SMILE

C1CNCCN1

InChI

1S/C4H10N2/c1-2-6-4-3-5-1/h5-6H,1-4H2
GLUUGHFHXGJENI-UHFFFAOYSA-N

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Categorie correlate

Avvertenze

Danger

Indicazioni di pericolo

H228,H314,H317,H334,H361fd

Classi di pericolo

Eye Dam. 1 - Flam. Sol. 1 - Repr. 2 - Resp. Sens. 1B - Skin Corr. 1B - Skin Sens. 1B

Codice della classe di stoccaggio

4.1B - Flammable solid hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 1

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificati d'analisi (COA)

Lot/Batch Number
BCCL6236
BCCL8124
BCCL7478
BCCL4605
BCCL1296

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Mitsunori Kono et al.
Bioorganic & medicinal chemistry, 21(1), 28-41 (2012-12-12)
A series of piperazine ureas was designed, synthesized, and evaluated for their potential as novel orally available fatty acid amide hydrolase (FAAH) inhibitors that are therapeutically effective against pain. We carried out an optimization study of the lead compound 3
R A Lovell
The Veterinary clinics of North America. Small animal practice, 20(2), 453-468 (1990-03-01)
Review of all reports involving anthelmintics in dogs and cats to the IAPIC between January 1, 1986 and August 10, 1988, revealed that ivermectin (extra-label use) and piperazine accounted for over 50% of the calls assessed as toxicoses and suspected
Janie Sheridan et al.
Drug and alcohol review, 26(3), 335-343 (2007-04-25)
In this Harm Reduction Digest Sheridan, Butler, Wilkins and Russell address the emergent phenomenon of so-called 'legal party pills' which have become a significant drug issue in New Zealand and elsewhere. Although banned in a number of countries, they are
John A Christopher et al.
Journal of medicinal chemistry, 56(9), 3446-3455 (2013-03-23)
Biophysical fragment screening of a thermostabilized β1-adrenergic receptor (β1AR) using surface plasmon resonance (SPR) enabled the identification of moderate affinity, high ligand efficiency (LE) arylpiperazine hits 7 and 8. Subsequent hit to lead follow-up confirmed the activity of the chemotype
Julio H K Rozenfeld et al.
Biochimica et biophysica acta, 1848(1 Pt A), 127-133 (2014-10-16)
In this work, the bilayer structure of novel cationic lipid diC16-amidine was compared to the one of zwitterionic dipalmitoyl phosphatidylcholine ( DPPC), which shares the same hydrophobic domain. Differential scanning calorimetry shows that DPPC and diC16-am idine bilayers have similar
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