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:
Molecular Weight:
90.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-474-2
Beilstein/REAXYS Number:
741859
MDL number:
Assay:
≥96.5% (GC)
Form:
solid
grade
purum
Quality Level
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
SMILES string
NCC(O)CN
InChI
1S/C3H10N2O/c4-1-3(6)2-5/h3,6H,1-2,4-5H2
InChI key
UYBWIEGTWASWSR-UHFFFAOYSA-N
Gene Information
rat ... Grin2a(24409)
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.
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signalword
Warning
hcodes
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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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
Y W Hu et al.
Canadian journal of physiology and pharmacology, 60(12), 1493-1498 (1982-12-01)
The effect of diaminopropanol, an inhibitor of polyamine synthesis, on the metabolic response of liver to insulin was studied in streptozotocin-diabetic rats. Insulin elicited a prompt and very marked increase in ornithine and S-adenosylmethionine decarboxylase activities and in putrescine concentration.
L Alhonen-Hongisto
The Biochemical journal, 190(3), 747-754 (1980-09-15)
1. The mechanism of stimulation of S-adenosylmethionine decarboxylase (EC 4.1.1.50) activity by inhibitors of ornithine decarboxylase (EC 4.1.1.17), namely dl-alpha-difluoromethylornithine, 1,3-diaminopropane and 1,3-diaminopropan-2-ol, was studied in Ehrlich ascites-tumour cells grown in suspension cultures. 2. Difluoromethylornithine and diaminopropane, although decreasing the
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 33262-25G-F | 04061826736944 |
| 33262-5G-F | 04061837008122 |