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A9754

Sigma-Aldrich

2-Amino-2-methyl-1,3-propanediol

≥99%

Synonym(s):

AMPD, Ammediol

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About This Item

Linear Formula:
(HOCH2)2C(NH2)CH3
CAS Number:
115-69-5
Molecular Weight:
105.14
Beilstein:
635708
EC Number:
204-100-7
MDL number:
MFCD00004678
UNSPSC Code:
12161700
PubChem Substance ID:
24891493
NACRES:
NA.25

vapor density

3.63 (vs air)

Quality Level

300

vapor pressure

~10 mmHg ( 152 °C)

Assay

≥99%

form

crystalline

pH

10.5-11.5 (25 °C, 105.1 g/L)

useful pH range

7.8-9.7

pKa (25 °C)

8.8

bp

151 °C/10 mmHg (lit.)

mp

100-110 °C (lit.)

solubility

H2O: 100 mg/mL, clear to slightly hazy, colorless to very faintly yellow

application(s)

diagnostic assay manufacturing

SMILES string

CC(N)(CO)CO

InChI

1S/C4H11NO2/c1-4(5,2-6)3-7/h6-7H,2-3,5H2,1H3

InChI key

UXFQFBNBSPQBJW-UHFFFAOYSA-N

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Related Categories

Application

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.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

>212.0 °F

Flash Point(C)

> 100 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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2-Amino-2-methyl-1-propanol BioXtra, ≥95%

Sigma-Aldrich

A9199

2-Amino-2-methyl-1-propanol

3-Amino-1,2-propanediol for synthesis

Sigma-Aldrich

8.18522

3-Amino-1,2-propanediol

Masahiro Fukuyama et al.
Frontiers in cell and developmental biology, 9, 590333-590333 (2021-08-20)
Current approaches for human hair follicle (HF) regeneration mostly adopt cell-autonomous tissue reassembly in a permissive murine intracorporeal environment. This, together with the limitation in human-derived trichogenic starting materials, potentially hinders the bioengineering of human HF structures, especially for the
K Jung et al.
Clinica chimica acta; international journal of clinical chemistry, 102(2-3), 215-219 (1980-03-28)
The inhibitory effect of inorganic phosphate on the activity determination of isoenzymes of alkaline phosphatase (AP) in diethanolamine (DEA), glycine and 2-amino-2-methyl-1,3-propandiol (AMPD) buffer was studied. This effect depends on the buffer used and isoenzyme investigated. Especially the placental isoenzyme
Richard E Wooley et al.
Diseases of aquatic organisms, 59(3), 263-267 (2004-07-22)
The antimicrobial agents used to treat bacterial fish diseases are archaic, and their uses may result in the emergence of drug-resistant bacterial strains. This study evaluated the in vitro antimicrobial activity of combinations of Tricide and neomycin or oxytetracycline on
A A Lemmens et al.
Journal of chromatography, 320(1), 193-197 (1985-02-22)
Isotachophoresis seems a likely candidate for a reference method, as it is more accurate and precise than common routine methods. The response is highly linear and depends on a well defined transport number of the leading ion, stability of the
W Thormann et al.
Electrophoresis, 11(4), 298-304 (1990-04-01)
The isotachophoretic behavior of a model protein, serum albumin, was examined (i) by computer simulation, (ii) by capillary isotachophoresis in HPE 100 and Tachophor 2127, (iii) by continuous flow isotachophoresis in Elphor VaP 22 and the BIO-STREAM Separator and (iv)
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