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PHR1554

Supelco

Heptane

Pharmaceutical Secondary Standard; Certified Reference Material

Synonyme(s) :

Heptane

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About This Item

Formule linéaire :
CH3(CH2)5CH3
Numéro CAS:
Poids moléculaire :
100.20
Numéro Beilstein :
1730763
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 1304209

Densité de vapeur

3.5 (vs air)

Pression de vapeur

40 mmHg ( 20 °C)
83 mmHg ( 37.7 °C)

CofA (certificat d'analyse)

current certificate can be downloaded

Température d'inflammation spontanée

433 °F

Limite d'explosivité

7 %

Conditionnement

ampule of 3x1.2 mL each

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Indice de réfraction

n20/D 1.387 (lit.)

Point d'ébullition

98 °C (lit.)

Pf

−91 °C (lit.)

Densité

0.684 g/mL at 25 °C (lit.)

Application(s)

pharmaceutical (small molecule)

Format

neat

Température de stockage

2-30°C

Chaîne SMILES 

CCCCCCC

InChI

1S/C7H16/c1-3-5-7-6-4-2/h3-7H2,1-2H3

Clé InChI

IMNFDUFMRHMDMM-UHFFFAOYSA-N

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Description générale

Heptane is a non-polar organic solvent and a straight-chain alkane with seven carbon atoms. It is generally employed in the synthesis of pharmaceuticals and considered to be one of the green solvents.
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.

Application

Heptane may be used as a pharmaceutical reference solvent standard for the determination of the analyte in bulk drug and pharmaceutical formulations by gas chromatography.
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 LRAC0594 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.

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Central nervous system

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

24.8 °F - closed cup

Point d'éclair (°C)

-4 °C - closed cup


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Certificats d'analyse (COA)

Lot/Batch Number

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Les clients ont également consulté

Green process chemistry in the pharmaceutical industry
Cue BW and Zhang J
Green Chemistry Letters and Reviews, 2(4), 193-211 (2009)
What is a green solvent? A comprehensive framework for the environmental assessment of solvents
Capello C, et al.
Green Chemistry, 9(9), 927-934 (2007)
?467? Residual Solvents
USP43/NF38: United States Pharmacopeia and National Formulary
United States Pharmacopeia/National Formulary, 45(3), 6712-6712 (2019)
A generic static headspace gas chromatography method for determination of residual solvents in drug substance.
Cheng, et al.
Journal of Chromatography A, 1217(41), 6413-6421 (2010)
Gábor Csordás et al.
PloS one, 9(6), e98191-e98191 (2014-06-04)
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