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Key Documents

33262

Sigma-Aldrich

1,3-Diamino-2-propanol

purum, ≥96.5% (GC)

Sinonimo/i:

1,3-Diamino-2-hydroxypropane

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About This Item

Formula condensata:
NH2CH2CH(OH)CH2NH2
Numero CAS:
Peso molecolare:
90.12
Beilstein:
741859
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

Grado

purum

Livello qualitativo

Saggio

≥96.5% (GC)

Forma fisica

solid

Impurezze

≤2.0% water

Punto di fusione

40-44 °C (lit.)

Solubilità

water: soluble 1 g/10 mL

Gruppo funzionale

amine
hydroxyl

Temperatura di conservazione

2-8°C

Stringa SMILE

NCC(O)CN

InChI

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

Informazioni sul gene

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Categorie correlate

Applicazioni

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.

Pittogrammi

Exclamation mark

Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves


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I clienti hanno visto anche

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
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
S Yamamoto et al.
Chemical & pharmaceutical bulletin, 37(11), 3139-3141 (1989-11-01)
When Vibrio parahaemolyticus AQ 3627 was grown in the presence of 1,3-diaminopropan-2-ol (OH-Dap), a new compound accumulated in the cells. This was identified as hydroxynorspermidine (OH-Nspd), N-(3-aminopropyl)-1,3-diaminopropan-2-ol, by gas chromatography-mass spectrometry and thin-layer chromatography. It was also synthesized enzymatically from
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

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