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PHR1275

Supelco

Naphthalene

Pharmaceutical Secondary Standard; Certified Reference Material

Synonym(s):

Naphthalene

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About This Item

Empirical Formula (Hill Notation):
C10H8
CAS Number:
Molecular Weight:
128.17
Beilstein:
1421310
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 USP 1457083

vapor density

4.4 (vs air)

vapor pressure

0.03 mmHg ( 25 °C)

CofA

current certificate can be downloaded

autoignition temp.

978 °F

expl. lim.

5.9 %

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

218 °C (lit.)

mp

80-82 °C (lit.)

application(s)

pharmaceutical (small molecule)

format

neat

storage temp.

2-30°C

SMILES string

c1ccc2ccccc2c1

InChI

1S/C10H8/c1-2-6-10-8-4-3-7-9(10)5-1/h1-8H

InChI key

UFWIBTONFRDIAS-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. Naphthalene is produced from fossil fuels such as coal and petroleum. Its commercial applications include, the production of polyvinyl plastics, moth repellents, dyes, leather tanning agents, resins, 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 (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 LRAA0011 in the slot below. This is an example certificate only and may not be the lot that you receive.

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Flam. Sol. 2

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 3

Flash Point(F)

173.3 °F - closed cup

Flash Point(C)

78.5 °C - closed cup


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Toxicological Profile for Naphthalene, 1-methylnaphthalene, and 2-methylnaphthalene (2005)
Fabrice Gritti et al.
Journal of chromatography. A, 1352, 20-28 (2014-06-14)
The effect of the pressure on the dispersion of a low molecular weight compound along 0.508 and 1.016 mm i.d. × 50 cm long open circular tubes was investigated theoretically and experimentally. The theoretical predictions were based on the early
H Höke et al.
Toxicology, 126(1), 1-7 (1998-05-19)
Detailed knowledge does exist on the toxicological safety of diisopropylnaphthalene (DIPN). Its metabolism is the key to understanding its very low toxicity. The metabolic pathway of 2,6-DIPN in rats was found to proceed almost exclusively through oxidation of the isopropyl
Sidney J Stohs et al.
Toxicology, 180(1), 97-105 (2002-09-27)
Naphthalene is a bicyclic aromatic compound that has wide industrial and commercial applications. It is used as the starting material for the synthesis of other compounds, as a moth repellent, soil fumigant and lavatory deodorant. Most exposure occurs through low
K M Yen et al.
Critical reviews in microbiology, 15(3), 247-268 (1988-01-01)
In pseudomonads, naphthalene is catabolized in a series of reactions to salicylic acid, which is further degraded via the catechol meta-cleavage, ortho-cleavage, or gentisic acid pathway to Krebs cycle intermediates. The naphthalene catabolic genes have been located on self-transmissible plasmids

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