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Merck

A9199

2-Amino-2-methyl-1-propanol

BioXtra, ≥95%

Synonym(s):

β-Aminoisobutyl alcohol, AMP

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About This Item

Linear Formula:
(CH3)2C(NH2)CH2OH
CAS Number:
Molecular Weight:
89.14
UNSPSC Code:
12161700
NACRES:
NA.25
PubChem Substance ID:
EC Number:
204-709-8
Beilstein/REAXYS Number:
505979
MDL number:
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Product Name

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

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

vapor density

3 (vs air)

vapor pressure

<1 mmHg ( 25 °C)

product line

BioXtra

assay

≥95%

form

liquid

impurities

≤0.005% Phosphorus (P)
≤0.1% Insoluble matter

ign. residue

≤0.1%

refractive index

n20/D 1.4455 (lit.)

pH

11.0-12 (25 °C, 8.9 g/L)

useful pH range

9.0-10.5

pKa (25 °C)

9.7

bp

165 °C (lit.)

mp

24-28 °C (lit.)

solubility

H2O: 0.5 M at 20 °C, clear, colorless

density

0.934 g/mL at 25 °C (lit.)

anion traces

chloride (Cl-): ≤0.05%
sulfate (SO42-): ≤0.05%

cation traces

Al: ≤0.0005%
Ca: ≤0.0005%
Cu: ≤0.0005%
Fe: ≤0.0005%
K: ≤0.005%
Mg: ≤0.0005%
NH4+: ≤0.05%
Na: ≤0.005%
Pb: ≤0.001%
Zn: ≤0.0005%

Quality Level

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Application

2-Amino-2-methyl-1-propanol has been used as an component in enzyme assay for screening the alkaline phosphatase activity in sarcoma osteogenic (SaOS-2) cells..

Biochem/physiol Actions

2-Amino-2-methyl-1-propanol is a substituted aliphatic alcohol and is used majorly as a pH balancer in cosmetic formulations. It has phototoxic effect as it can interact and penetrate above the sebum layer. However, it is not carcinogenic.

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


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The morphogenetically active polymer, inorganic polyphosphate complexed with GdCl3, as an inducer of hydroxyapatite formation in vitro
Wang X, et al.
Biochemical Pharmacology, 102(6), 97-106 (2016)
Phototoxic assessment of a sunscreen formulation and its excipients: An in vivo and in vitro study
Hossy BH, et al.
Journal of Photochemistry and Photobiology. B, Biology, 173(6), 545-550 (2017)
Final amended report on safety assessment on aminomethyl propanol and aminomethyl propanediol
Burnett CL, et al.
International Journal of Toxicology, 28(6), 141S-161S (2009)
Muhammad Hasib-ur-Rahman et al.
Environmental science & technology, 46(20), 11443-11450 (2012-09-12)
One of the major drawbacks of aqueous alkanolamine based CO(2) capture processes is the requirement of significantly higher energy of regeneration. This weakness can be overcome by separating the CO(2)-captured product to regenerate the corresponding amine, thus avoiding the consumption
Chia-Chang Lin et al.
Journal of hazardous materials, 175(1-3), 344-351 (2009-11-17)
The removal of CO(2) from a 10 vol% CO(2) gas by chemical absorption with 30 wt% alkanolamine solutions containing monoethanolamine (MEA), piperazine (PZ), and 2-amino-2-methyl-1-propanol (AMP) in the cross-flow rotating packed bed (RPB) was investigated. The CO(2) removal efficiency increased

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