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About This Item
Quality Segment
agency
according to Ph. Eur., according to USP
vapor density
2.7 (vs air)
vapor pressure
0.42 mmHg ( 20 °C)
product line
SupraSolv®
assay
≥99.8% (GC)
form
liquid
autoignition temp.
573 °F
potency
28300 mg/kg LD50, oral (Rat), 40000 mg/kg LD50, skin (Rat)
expl. lim.
42 %, 63 °F
technique(s)
GC-HS: suitable
impurities
≤1 μg/g Every residual solvent of class 1 acc. to ICH, ≤10 μg/g Every residual solvent of class 2 acc. to ICH, ≤50 μg/g Every residual solvent of class 3 acc. to ICH, ≤0.05% Water
evapn. residue
≤3.0 mg/L
color
APHA: ≤10
refractive index
n20/D 1.479 (lit.)
kinematic viscosity
2.14 cSt
bp
189 °C (lit.)
mp
16-19 °C (lit.)
transition temp
flash point 87 °C
density
1.10 g/mL (lit.)
storage temp.
2-30°C
SMILES string
CS(C)=O
InChI
1S/C2H6OS/c1-4(2)3/h1-2H3
InChI key
IAZDPXIOMUYVGZ-UHFFFAOYSA-N
General description
Application
Features and Benefits
- Regulatory compliance with ICH Q3C, Ph. Eur., and USP residual solvent guidelines, directly supporting pharmaceutical quality control workflows
- Ultra-low intrinsic volatile impurity content, eliminating solvent-derived interferences in the headspace chromatogram and ensuring an unobstructed baseline
- Batch-to-batch consistency, ensuring reproducibility across analytical campaigns
Analysis Note
Other Notes
Legal Information
Disclaimer
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Storage Class
10 - Combustible liquids
flash_point_f
188.6 °F - closed cup
flash_point_c
87 °C - closed cup
Certificates of Analysis (COA)
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