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agency
BP
ChP
JPE
NF
Ph. Eur.
Quality Level
vapor density
3.4 (vs air)
vapor pressure
2.2 mmHg ( 20 °C)
5 mmHg ( 25 °C)
product line
EMPROVE® EXPERT
form
liquid
concentration
85%
technique(s)
API processing | salt formation: suitable
pH
<0.5 (20 °C, 100 g/L in H2O)
kinematic viscosity
30.5 cSt(20 °C)
bp
158 °C (lit.)
mp
~40 °C (lit.)
density
1.685 g/mL at 25 °C (lit.)
application(s)
liquid formulation
ophthalmics
pharma/biopharma processes
pharmaceutical
semi-solid formulation
storage temp.
2-30°C
SMILES string
OP(O)(O)=O
InChI
1S/H3O4P/c1-5(2,3)4/h(H3,1,2,3,4)
InChI key
NBIIXXVUZAFLBC-UHFFFAOYSA-N
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This Item | 1.93403 | PHR3222 | 4.80951 |
|---|---|---|---|
| concentration 85% | concentration - | concentration - | concentration - |
| application(s) liquid formulation | application(s) - | application(s) pharmaceutical small molecule | application(s) pharmaceutical |
| agency BP, JPE, Ph. Eur., ChP, NF | agency - | agency traceable to USP 1535802 | agency NF, Ph. Eur. |
| technique(s) API processing | salt formation: suitable | technique(s) - | technique(s) - | technique(s) - |
| form liquid | form - | form - | form liquid |
| density 1.685 g/mL at 25 °C (lit.) | density 1.685 g/mL at 25 °C (lit.) | density 1.685 g/mL at 25 °C (lit.) | density 1.053 g/cm3 at 20 °C |
General description
As part of our Emprove® Program, our raw materials are offered with extensive documentation facilitating compliance of your pharma and biopharma product, full supply chain transparency and risk mitigation. Our SAFC® portfolio of high-quality products for biopharmaceutical and pharmaceutical formulation and production withstands strict quality control procedures and is produced according to applicable cGMP guidelines.
Application
Other Notes
Legal Information
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B
Storage Class
8B - Non-combustible corrosive hazardous materials
wgk_germany
WGK 1
flash_point_f
does not flash
flash_point_c
does not flash
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