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Merck
CN

33262

1,3-Diamino-2-propanol

purum, ≥96.5% (GC)

Synonym(s):

1,3-Diamino-2-hydroxypropane

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About This Item

Linear Formula:
NH2CH2CH(OH)CH2NH2
CAS Number:
616-29-5
Molecular Weight:
90.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
329754481
EC Number:
210-474-2
Beilstein/REAXYS Number:
741859
MDL number:
MFCD00008142
Assay:
≥96.5% (GC)
Form:
solid

Key Documents

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InChI key

UYBWIEGTWASWSR-UHFFFAOYSA-N

InChI

1S/C3H10N2O/c4-1-3(6)2-5/h3,6H,1-2,4-5H2

SMILES string

NCC(O)CN

grade

purum

assay

≥96.5% (GC)

form

solid

impurities

≤2.0% water

mp

40-44 °C (lit.)

solubility

water: soluble 1 g/10 mL

functional group

amine, hydroxyl

storage temp.

2-8°C

Quality Level

200

Gene Information

rat ... Grin2a(24409)

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Application

1,3-Diamino-2-propanol was used in the synthesis of poly(2-hydroxypropylene imine), poly(2-hydroxypropylene imine ethylene imine) and poly(hydroxypropylene imine propylene imine). It was also used in the synthesis of tetranuclear mixed ligand copper(II) complex of a pyrazole containing Schiff base and a hydroxyhexahydropyrimidylpyrazole group.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCN2651
BCCH9954
BCCJ0325
BCCF1842
BCCB3937

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Sachindranath Pal et al.
Inorganic chemistry, 44(11), 3880-3889 (2005-05-24)
A tetranuclear mixed ligand copper(II) complex of a pyrazole containing Schiff base and a hydroxyhexahydropyrimidylpyrazole and copper(II) and nickel(II) complexes of the Schiff base having N-donor atoms have been investigated. A 2 equiv amount of 5-methyl-3-formylpyrazole (MPA) and 2 equiv
L Alhonen-Hongisto et al.
The Biochemical journal, 188(2), 491-501 (1980-05-15)
The anti-proliferative effects of 1,1'-[(methylethanediylidene)dinitrilo]diguanidine [methylglyoxal bis(guanylhydrazone)] and 1,1'-[(metHYLETHANEDIYLIDENE)dinitrilo]bis-(3-aminoguaNIDINE) HAVE BEEN STUDIED IN Ehrlich ascites carcinoma cells grown in suspension cultures. Both compounds are potent inhibitors of S-adenosyl-L-methionine decarboxylase from the tumour cells. In the presence of putrescine (but not
J M Matés et al.
Biochemical pharmacology, 42(5), 1045-1052 (1991-08-08)
Ornithine decarboxylase (ODC) activity of Ehrlich carcinoma cells was increased more than 36-fold after being maintained for 3.5 hr in vitro in a special chamber which allowed continuous perifusion with 0.5 mM ornithine; if incubated in vitro without perifusion the
M Mach et al.
The Biochemical journal, 202(1), 153-162 (1982-01-15)
Inhibitors of polyamine synthesis (alpha-methylornithine and 1,3-diaminopropan-2-ol) were used to study the relationship between polyamine synthesis and specific methylations of tRNA in Dictyostelium discoideum during vegetative growth. Polyamine concentrations were found to be 10 mM for putrescine, 1.6 mM for
H Raunio et al.
Biochemical pharmacology, 31(2), 189-193 (1982-01-15)
The induction of aryl hydrocarbon and ornithine decarboxylase by benz[a]-anthracene in the presence or absence of ornithine decarboxylase inhibitors was studied in three different cell culture systems. An almost complete abolishment of ornithine decarboxylase activity by 1,3-diamino-2-propanol or alpha-difluoremethyl ornithine
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