Skip to Content
Merck
CN

01-3780

2-Amino-2-methyl-1-propanol

SAJ first grade, ≥98.0%

Synonym(s):

β-Aminoisobutyl alcohol, AMP

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
(CH3)2C(NH2)CH2OH
CAS Number:
Molecular Weight:
89.14
EC Number:
204-709-8
UNSPSC Code:
12352104
PubChem Substance ID:
Beilstein/REAXYS Number:
505979
MDL number:
Assay:
≥98.0%
Grade:
SAJ first grade
Bp:
165 °C (lit.)
Vapor pressure:
<1 mmHg ( 25 °C)
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI

1S/C4H11NO/c1-4(2,5)3-6/h6H,3,5H2,1-2H3

InChI key

CBTVGIZVANVGBH-UHFFFAOYSA-N

SMILES string

CC(C)(N)CO

grade

SAJ first grade

vapor density

3 (vs air)

vapor pressure

<1 mmHg ( 25 °C)

assay

≥98.0%

availability

available only in Japan

dilution

(for analytical testing)

refractive index

n20/D 1.4455 (lit.)

useful pH range

9.0-10.5

pKa (25 °C)

9.7

bp

165 °C (lit.)

mp

24-28 °C (lit.)

density

0.934 g/mL at 25 °C (lit.)

Looking for similar products? Visit Product Comparison Guide

pictograms

Corrosion

signalword

Danger

Hazard Classifications

Aquatic Chronic 3 - Eye Dam. 1 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk

WGK 1

flash_point_f

179.8 °F - closed cup

flash_point_c

82.1 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

K Lewandrowski et al.
Clinical chemistry, 38(11), 2286-2294 (1992-11-11)
We evaluated N-methyl-D-glucamine (MEG) as a buffer for assay of alkaline phosphatase (ALP; EC 3.1.3.1) and compared the MEG-based assay with the current International Federation of Clinical Chemistry Reference Method for ALP (IFCC/RM/ALP), in which 2-amino-2-methyl-1-propanol (AMP) is the pH
Shia-Chung Chen et al.
Journal of hazardous materials, 179(1-3), 692-700 (2010-04-15)
In this study, the recovery of carbon dioxide using an absorbent composed of 2-amino-2-methyl-l-propanol (AMP)+monoethanolamine (MEA)+piperazine (PZ) in polytetrafluoroethylene (PTFE) membrane contactors was investigated. Experiments were conducted using various gas flow rates, liquid flow rates, absorbent blends, and pore size
M Lamberto et al.
Analytical biochemistry, 230(2), 224-228 (1995-09-20)
The effect of derivatization with 2-amino-2-methyl-propanol on trans-3-hexadecenoic acid was investigated as part of the identification of the trans-3-hexadecenoic acid in two Nova Scotian seaweeds. After the extraction of the total fatty acids and their methylation, the monoenoic trans fraction
R A Stinson
Clinical chemistry, 39(11 Pt 1), 2293-2297 (1993-11-01)
Nine different isoenzymes and (or) isoforms of alkaline phosphatase (ALP; EC 3.1.3.1) from human tissue were studied with respect to Km and Vmax values for p-nitrophenyl phosphate (p-NPP) in seven different potential phosphoacceptors/buffers. Generally, the phosphoacceptors/buffers with the lowest affinity
Won-Joon Choi et al.
Journal of environmental sciences (China), 21(7), 907-913 (2009-10-30)
The carbon dioxide (CO2) removal efficiency, reaction rate, and CO2 loading into aqueous blended monoethanolamine (MEA) + 2-amino-2-methyl-1-propanol (AMP) solutions to enhance absorption characteristics of MEA and AMP were carried out by the absorption/regeneration process. As a result, compared to

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service