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PHR1548

Supelco

Propyl Acetate

Pharmaceutical Secondary Standard; Certified Reference Material

Synonym(s):

Propyl acetate

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About This Item

Linear Formula:
CH3COOCH2CH2CH3
CAS Number:
109-60-4
Molecular Weight:
102.13
Beilstein/REAXYS Number:
1740764
EC Number:
203-686-1
MDL number:
MFCD00009372
UNSPSC Code:
41116107
PubChem Substance ID:
329823457
NACRES:
NA.24

grade

certified reference material
pharmaceutical secondary standard

Quality Level

300

agency

traceable to USP 1576402

vapor density

3.5 (vs air)

vapor pressure

25 mmHg ( 20 °C)

API family

propyl acetate

CofA

current certificate can be downloaded

autoignition temp.

842 °F

expl. lim.

1.7 %, 37 °F
8 %

packaging

ampule of 3x1.2 mL

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.384 (lit.)

bp

102 °C (lit.)

mp

−95 °C (lit.)

density

0.888 g/mL at 25 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-30°C

SMILES string

CCCOC(C)=O

InChI

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

InChI key

YKYONYBAUNKHLG-UHFFFAOYSA-N

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General description

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.

Analysis Note

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

Other Notes

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.

Footnote

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.

Recommended products

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.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system

supp_hazards

EUH066

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

53.2 °F - closed cup

flash_point_c

11.8 °C - closed cup

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
LRAD1151
LRAB4507
LRAA4464

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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)
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
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
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