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Key Documents

249467

Sigma-Aldrich

Propyl chloroformate

98%

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About This Item

Formule linéaire :
ClCO2CH2CH2CH3
Numéro CAS:
Poids moléculaire :
122.55
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22

Pression de vapeur

0.87 psi ( 20 °C)

Pureté

98%

Forme

liquid

Indice de réfraction

n20/D 1.404 (lit.)

Point d'ébullition

105-106 °C (lit.)

Solubilité

benzene: miscible(lit.)
chloroform: miscible(lit.)
diethyl ether: miscible(lit.)

Densité

1.09 g/mL at 25 °C (lit.)

Température de stockage

2-8°C

Chaîne SMILES 

CCCOC(Cl)=O

InChI

1S/C4H7ClO2/c1-2-3-7-4(5)6/h2-3H2,1H3

Clé InChI

QQKDTTWZXHEGAQ-UHFFFAOYSA-N

Application

Propyl chloroformate has been used:
  • as derivatization reagent in quantification of dopamine, serotonin and norepinephrine in human urine by solid phase microextraction-gas chromatography-triple quadrupole mass spectrometry
  • in the preparation of dipropyl 3,6-diphenyl-1,2-dihydro-1,2,4,5-tetrazine-1,2-dicarboxylate

Pictogrammes

FlameSkull and crossbonesCorrosion

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

71.6 °F

Point d'éclair (°C)

22 °C

Équipement de protection individuelle

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Consulter la Bibliothèque de documents

Guo-Wu Rao et al.
Acta crystallographica. Section C, Crystal structure communications, 59(Pt 5), o281-o282 (2003-05-14)
The title compound, C(22)H(24)N(4)O(4), was prepared from propyl chloroformate and 3,6-diphenyl-1,2-dihydro-s-tetrazine. This reaction yields the title compound rather than dipropyl 3,6-diphenyl-1,4-dihydro-s-tetrazine-1,4-dicarboxylate. The 2,3-diazabutadiene group in the central six-membered ring is not planar; the C=N double-bond length is 1.285 (2) A
Jake P Violi et al.
Ecotoxicology and environmental safety, 172, 72-81 (2019-01-27)
Environmental exposure to the amino acid β-methylamino-L-alanine (BMAA) was linked to the high incidence of neurodegenerative disease first reported on the island of Guam in the 1940s and has more recently been implicated in an increased incidence of amyotrophic lateral
Nur Cebi et al.
Food chemistry, 248, 8-13 (2018-01-14)
An effective and simultaneous liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was used with the aim of quantifying monosodium glutamate (MSG) in foodstuffs, such as chips, taste cubes, sauces and soups. The results were linear (R
Brendan J Main et al.
Harmful algae, 74, 10-18 (2018-05-05)
The emerging toxin β-methylamino-l-alanine (BMAA) has been linked to the development of a number of neurodegenerative diseases in humans including amyotrophic lateral sclerosis (ALS), Alzheimer's disease, and Parkinson's disease. BMAA has been found to be produced by a range of
Laura Louise Scott et al.
Neurotoxicity research, 33(1), 6-14 (2017-05-05)
Chronic inhalation of aerosolized β-N-methylamino-L-alanine (BMAA) could serve as potenital route for exposure to this cyanobacterial neurotoxin implicated in the development of neurodegenerative disease. We investigated environmental aerosol BMAA loads and the fate of inhaled isotopically labeled aerosolized BMAA in

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