Fortfahren mit
08569
2-Amino-2-methyl-1,3-propandiol
BioUltra, ≥99.5% (NT)
Synonym(e):
AMPD, Ammediol
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| Packungsgröße | SKU | Verfügbarkeit | Preis |
|---|---|---|---|
| 100 g | Warenkorb auf Verfügbarkeit prüfen | € 203,00 |
Über diesen Artikel
Lineare Formel:
(HOCH2)2C(NH2)CH3
CAS-Nummer:
Molekulargewicht:
105.14
UNSPSC Code:
12161700
NACRES:
NA.25
PubChem Substance ID:
EC Number:
204-100-7
Beilstein/REAXYS Number:
635708
MDL number:
Technischer Dienst
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Unterstützung erhaltenvapor density
3.63 (vs air)
Quality Level
vapor pressure
~10 mmHg ( 152 °C)
product line
BioUltra
assay
≥99.5% (NT)
form
crystalline
impurities
insoluble matter, passes filter test
pH
10.5-11.5 (25 °C, 1 M in H2O)
useful pH range
7.8-9.7
pKa (25 °C)
8.8
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Verwandte Kategorien
Application
2-Amino-2-methyl-1,3-propanediol can be used to study biological buffers. 2-Amino-2-methyl-1,3-propanediol has been used in a study to afford a new family of isostructural octanuclear Cu4Ln4 complexes. 2-Amino-2-methyl-1,3-propanediol has also been used in a study to improve cooling refrigerants for low-temperature applications.
Buffer component in a SDS-gradient gel electrophoresis system that separates polypeptides in the molecular weight range of 1500 to 100,000. Used as a spacer in isotachophoresis of proteins. Also used as a buffer for the determination of alkaline phosphatase activity.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Lagerklasse
11 - Combustible Solids
wgk
WGK 1
flash_point_f
>212.0 °F
flash_point_c
> 100 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
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S Canepari et al.
Talanta, 44(11), 2059-2067 (2008-10-31)
Formation constants of the silver(I) complexes with some amino-alcohols have been determined at 25 degrees C in 0.5 M KNO(3) by means of two independent potentiometric measurements employing glass and silver electrode. The ligands considered are: sec-butylamine, 2-amino-1-propanol, 2-amino-1-methoxy-propane, 2-amino-2-methyl-1-propanol
A new family of octanuclear Cu4Ln4 (Ln = Gd, Tb and Dy) spin clusters
Alley, K.G., et al.
Dalton Transactions, 7, 59-63 (2008)
Takayuki Yakura et al.
Chemical & pharmaceutical bulletin, 55(9), 1385-1389 (2007-09-11)
Dirhodium(II)-catalyzed C-H amination reaction of (S)-3-(tert-butyldimethylsilyloxy)-2-methylpropyl carbamate, which was easily prepared from methyl (S)-2-methyl-3-hydroxypropanoate, proceeded more smoothly than those of their 2-(methoxycarbonyl)propyl derivative to give the corresponding oxazolidinone in excellent yield. The resulting oxazolidinone was converted efficiently into both (R)-monoprotected
H Kikuchi et al.
The Tohoku journal of experimental medicine, 173(4), 391-397 (1994-08-01)
The method by MacQueen and Plaut was modified to devise simple microdetermination method of l-lactate which is applicable to deproteinized blood sample. Blood was deproteinized with addition of 25% (w/w) trichloroacetic acid (TCA), and 0.075 M 2-amino-2-methyl-1, 3-propanediole (AMPD) was
Karen M O'Connor et al.
Journal of pharmaceutical sciences, 91(10), 2271-2281 (2002-09-13)
Dissolution of diclofenac from compressed discs containing mixtures of a diclofenac salt and a basic excipient, in various w/w ratios, was examined. Two diclofenac salts, diclofenac deanol (DDNL) and diclofenac tert-butylamine, and the basic excipient 2-amino-2-methyl-1,3-propanediol (AMPD) were examined. Inclusion
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 218170-5G | 04061838775306 |
| 218170-25G | 04061838252531 |
| 218170-1G | 04061838775290 |
| 218170-100G | 04061838775283 |
| 08569-25G | 04061838652546 |
| 08569-100G | 04061833605356 |
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