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404624

3-Aminopyrrolidine dihydrochloride

Name: 3-Aminopyrrolidine dihydrochloride
Brand: ALDRICH

98%

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About This Item

Empirical Formula (Hill Notation):

C₄H₁₀N₂ · 2HCl

CAS Number:

103831-11-4

Molecular Weight:

159.06

NACRES:

NA.22

PubChem Substance ID:

24865261

UNSPSC Code:

12352100

MDL number:

MFCD00060176

Assay:

98%

Form:

solid

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Properties

Quality Level

100

assay

98%

form

solid

mp

>300 °C (lit.)

SMILES string

Cl[H].Cl[H].NC1CCNC1

InChI

1S/C4H10N2.2ClH/c5-4-1-2-6-3-4;;/h4,6H,1-3,5H2;2*1H

InChI key

NJPNCMOUEXEGBL-UHFFFAOYSA-N

Description

General description

3-Aminopyrrolidine dihydrochloride (3-pyrrolidinamine dihydrochloride) is one of the key intermediate of tosufloxacin and other quinolone antibiotics.

Application

3-Aminopyrrolidine dihydrochloride is the suitable reagent used as an internal standard for the quantitative analysis of amino acids in bio-fluids. (R,S) 3-Aminopyrrolidine dihydrochloride may be used in the preparation of cis-[PdCl₂(pyrr)] and cis-[PtCl₂(pyrr)] (pyrr= (R,S)-3-aminopyrrolidine) complexes.

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

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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Synthesis of 3-Aminopyrrolidine and its N-alkylating Derivatives [J].

Run-pu SHEN, et al.

Journal of Chemical Engineering of Chinese Universities / Gao Xiao Hua Xue Gong Cheng Xue Bao, 4, 014-014 (2003)

Pd (II) and Pt (II)(R, S)-3-aminopyrrolidine complexes. Reactions with 9-ethylguanine and study of their antiproliferative activity.

Riera X, et al.

Inorgorganica Chimica Acta, 339, 253-264 (2002)

Metabolome profiling of various seaweed species discriminates between brown, red, and green algae.

Shahlizah Sahul Hamid et al.

Planta, 249(6), 1921-1947 (2019-03-21)

Among seaweed groups, brown algae had characteristically high concentrations of mannitol, and green algae were characterised by fructose. In red algae, metabolite profiles of individual species should be evaluated. Seaweeds are metabolically different from terrestrial plants. However, general metabolite profiles

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Global Trade Item Number

SKU	GTIN
404624-25G	04061833398487
404624-5G	04061833372494