3-Pyrrolidinamine dihydrochloride

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Names

[ CAS No. ]:
103831-11-4

[ Name ]:
3-Pyrrolidinamine dihydrochloride

[Synonym ]:
Pyrrolidin-3-amine dihydrochloride
3-aminopyrrolidine dihydrochloride
3-Pyrrolidinamine dihydrochloride
MFCD00060176
pyrrolidin-3-amine,dihydrochloride
3-Pyrrolidinamine, hydrochloride (1:2)

Chemical & Physical Properties

[ Density]:
1.413

[ Boiling Point ]:
214.5ºC at 760 mmHg

[ Melting Point ]:
>300 °C(lit.)

[ Molecular Formula ]:
C4H12Cl2N2

[ Molecular Weight ]:
159.057

[ Flash Point ]:
83.5ºC

[ Exact Mass ]:
158.037750

[ PSA ]:
38.05000

[ LogP ]:
1.94010

[ Vapour Pressure ]:
1.24mmHg at 25°C

[ Water Solubility ]:
Slightly soluble.

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi:Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36-S37/39

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2933990090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • (3R)-3-azido-1-(phenylmethyl)pyrrolidine
  • 3-Pyrrolidinamine

DownStream

  • 1-Boc-3-aminopyrrolidine

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Metabolic Profiling with Gas Chromatography-Mass Spectrometry and Capillary Electrophoresis-Mass Spectrometry Reveals the Carbon-Nitrogen Status of Tobacco Leaves Across Different Planting Areas.

J. Proteome Res. 15 , 468-76, (2016)

The interaction between carbon (C) and nitrogen (N) metabolism can reflect plant growth status and environmental factors. Little is known regarding the connections between C-N metabolism and growing r...

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

Inorganica Chim. Acta 339 , 253-64, (2002)

Synthesis of 3-Aminopyrrolidine and its N-alkylating Derivatives [J]. Run-pu SHEN, et al.

J. Chem. Eng. Chin. Univ. 4 , 014, (2003)


More Articles

Related Compounds

  • 3-Pyrrolidinamine dihydrochloride
  • (3R)-3-Pyrrolidinamine dihydrochloride
  • 1-Ethyl-3-pyrrolidinamine dihydrochloride
  • 1-Methyl-3-pyrrolidinamine dihydrochloride
  • (3R)-1-Ethyl-3-pyrrolidinamine dihydrochloride
  • N,N-Dimethyl-3-pyrrolidinamine dihydrochloride
  • (3S)-7-Ethyl-2,3-dihydro-1-benzofuran-3-amine
  • 1-Hexyl-3-methylimidazolium perfluorobutanesulfonate
  • Methyl (2S)-2-(thieno[2,3-d]pyrimidin-4-ylamino)propanoate
  • 1-(4-Methoxybutyl)-1H-indole-4-carboxylic acid methyl ester
  • (2Z)-2-Cyano-N-(furan-2-ylmethyl)-2-[2-(4-methoxyphenyl)-6-methylchromen-4-ylidene]acetamide
  • (Z)-3-(1,3-Benzodioxol-5-yl)-2-cyano-N-(3-piperidin-1-ylsulfonylphenyl)prop-2-enamide
  • 2-cyano-N-(2,3-dihydro-1,4-benzodioxin-6-yl)-3-(naphthalen-2-yl)prop-2-enamide
  • Tert-butyl (2-(6-((tetrahydrothiophen-3-yl)oxy)nicotinamido)ethyl)carbamate
  • N-((5-(hydroxymethyl)furan-2-yl)methyl)-6-((tetrahydrothiophen-3-yl)oxy)nicotinamide
  • N-(1-methyl-1H-indazol-5-yl)-6-((tetrahydrothiophen-3-yl)oxy)nicotinamide
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