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PHR1313

Supelco

m-Xylene

Pharmaceutical Secondary Standard; Certified Reference Material

Synonym(s):

1,3-Dimethylbenzene

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About This Item

Linear Formula:
C6H4(CH3)2
CAS Number:
Molecular Weight:
106.17
Beilstein:
605441
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

certified reference material
pharmaceutical secondary standard

Quality Level

Agency

traceable to NIST 3004
traceable to USP 1601849

vapor density

3.7 (vs air)

CofA

current certificate can be downloaded

autoignition temp.

982 °F

expl. lim.

7 %

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.497 (lit.)

bp

138-139 °C (lit.)

mp

−48 °C (lit.)

density

0.868 g/mL at 25 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-30°C

SMILES string

Cc1cccc(C)c1

InChI

1S/C8H10/c1-7-4-3-5-8(2)6-7/h3-6H,1-2H3

InChI key

IVSZLXZYQVIEFR-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. m-Xylene is widely used as a residual solvent (RS) or organic volatile impurity (OVI) in pharmaceutical formulations.

Application

m-Xylene may be used as a pharmaceutical reference standard for the determination of the analyte in tablet formulations by chromatography. It can also be used as a residual solvent standard for the quantification of the analyte in tablet formulations by headspace gas chromatography (HS-GC) with flame ionization detection (FID) technique.
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 (PhEur) 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 LRAB3625 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.

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Aquatic Chronic 3 - Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point(F)

80.6 °F - closed cup

Flash Point(C)

27 °C - closed cup


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Customers Also Viewed

m-Xylene
USP43-NF38
United States Pharmacopeia/National Formulary, 6218-6218 (2013)
Determination of Organic Volatile Impurities in Twenty-Three Different Coated Tablet Formulations Using Headspace Gas Chromatography with Flame Ionization Detection Technique
Latif A, et al.
Pharmaceutica Analytica Acta, 8, 553-553 (2017)
Dragana Bozinovski et al.
FEMS microbiology ecology, 81(1), 134-144 (2012-03-01)
A sulfate-reducing consortium maintained for several years in the laboratory with m-xylene as sole source of carbon and energy was characterized by terminal restriction fragment length polymorphism (T-RFLP) fingerprinting of PCR-amplified 16S rRNA genes and stable isotope probing of proteins
Shu Cheng et al.
Environmental health perspectives, 119(12), 1712-1718 (2011-08-13)
Computational modeling of the absorption, distribution, metabolism, and excretion of chemicals is now theoretically able to describe metabolic interactions in realistic mixtures of tens to hundreds of substances. That framework awaits validation. Our objectives were to a) evaluate the conditions
Michalis Koutinas et al.
Environmental microbiology, 12(6), 1705-1718 (2010-06-18)
The structure of the extant transcriptional control network of the TOL plasmid pWW0 born by Pseudomonas putida mt-2 for biodegradation of m-xylene is far more complex than one would consider necessary from a mere engineering point of view. In order

Protocols

Protocol for HPLC Analysis of Xylene Isomers on Discovery® Zr-Carbon

ASTM D6526: GC Analysis of Impurities in Toluene on SLB®-IL100, 60 m Column

GC Analysis of Xylene Isomers on SLB®-IL60 - The cresol (methylphenol) isomers are also precursors to many chemicals. This chromatogram of a mix of aromatic and methylphenol compounds was generated using an SLB-IL60 ionic liquid column. Its interaction mechanisms allow the separation of all three xylene isomers, and all three cresol isomers.

Technical article page on -US EPA Method 8015 (modified): GC Analysis of Gasoline Range Organics (GRO) on Equity®-1 after Purge & Trap using "M" Trap

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