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Key Documents

PHR1548

Supelco

Propyl acetate

Pharmaceutical Secondary Standard; Certified Reference Material

Synonyme(s) :

Propyl acetate

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About This Item

Formule linéaire :
CH3COOCH2CH2CH3
Numéro CAS:
Poids moléculaire :
102.13
Numéro Beilstein :
1740764
Numéro CE :
Numéro MDL:
Code UNSPSC :
41116107
ID de substance PubChem :
Nomenclature NACRES :
NA.24

Qualité

certified reference material
pharmaceutical secondary standard

Niveau de qualité

Agence

traceable to USP 1576402

Densité de vapeur

3.5 (vs air)

Pression de vapeur

25 mmHg ( 20 °C)

Famille d'API

propyl acetate

CofA (certificat d'analyse)

current certificate can be downloaded

Température d'inflammation spontanée

842 °F

Limite d'explosivité

1.7 %, 37 °F
8 %

Conditionnement

ampule of 3x1.2 mL

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Indice de réfraction

n20/D 1.384 (lit.)

Point d'ébullition

102 °C (lit.)

Pf

−95 °C (lit.)

Densité

0.888 g/mL at 25 °C (lit.)

Application(s)

pharmaceutical (small molecule)

Format

neat

Température de stockage

2-30°C

Chaîne SMILES 

CCCOC(C)=O

InChI

1S/C5H10O2/c1-3-4-7-5(2)6/h3-4H2,1-2H3

Clé InChI

YKYONYBAUNKHLG-UHFFFAOYSA-N

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Description générale

Pharmaceutical secondary standards for application in quality control, provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards. Propyl Acetate is the propyl ester of acetic acid. It is a volatile component of Beaufort cheese, apples, bananas, nectarines and Concord grape juice. It is widely used as a printing ink solvent and finds applications as a solvent for chlorinated rubber, heat reactive phenolics, cellulose nitrate, etc.

Application

These Secondary Standards are qualified as Certified Reference Materials. These are suitable for use in several analytical applications including but not limited to pharma release testing, pharma method development for qualitative and quantitative analyses, food and beverage quality control testing, and other calibration requirements.

Remarque sur l'analyse

These secondary standards offer multi-traceability to the USP, EP and BP primary standards, where they are available.

Autres remarques

This Certified Reference Material (CRM) is produced and certified in accordance with ISO 17034 and ISO/IEC 17025. All information regarding the use of this CRM can be found on the certificate of analysis.

Note de bas de page

To see an example of a Certificate of Analysis for this material enter LRAA4464 in the slot below. This is an example certificate only and may not be the lot that you receive.

Produits recommandés

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Pictogrammes

FlameExclamation mark

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

Organes cibles

Central nervous system

Risques supp

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

53.2 °F - closed cup

Point d'éclair (°C)

11.8 °C - closed cup


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Certificats d'analyse (COA)

Lot/Batch Number

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Les clients ont également consulté

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Handbook of Environmental Fate and Exposure Data For Organic Chemicals, 4(10) (1993)
Handbook of Environmental Fate and Exposure Data For Organic Chemicals, 4(10) (1993)
Handbook of Environmental Fate and Exposure Data For Organic Chemicals, 4(10) (1993)
M R Menlyadiev et al.
The Analyst, 140(9), 2995-3002 (2015-03-25)
Proton-bound dimers were dissociated to protonated monomers in air at ambient pressure and temperature using electric fields of ultrahigh Field Asymmetric Ion Mobility Spectrometry (ultraFAIMS) with the onset of dissociation for ethyl acetate as 96 Td and for dimethyl methyl
Anthony Sclafani et al.
American journal of physiology. Regulatory, integrative and comparative physiology, 307(12), R1448-R1457 (2014-10-17)
Recent studies indicate that, unlike glucose, fructose has little or no post-oral preference conditioning actions in C57BL/6J (B6) mice. The present study determined whether this is also the case for FVB mice, which overconsume fructose relative to B6 mice. In

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