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1.04002

SAFC

Formaldehyde solution

37%, EMPROVE® EVOLVE

Pharma Manufacturing

Synonym(s):

Formaline solution, Methanal solution, Methylaldehyde solution

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About This Item

UNSPSC Code:
12352114

description

stabilized with about 10% methanol Ph Eur,BP,USP

Quality Level

400

product line

EMPROVE® EVOLVE

form

liquid

autoignition temp.

300 °C (Formaldehyde)

expl. lim.

7-73 % (v/v) Formaldehyde)

concentration

36.5-38% (iodometric)
37%

pH

2.8-4.0 (20 °C in H2O)

bp

93-96 °C/1013 hPa

mp

<-15 °C

transition temp

flash point 62 °C (Formaldehyde)

density

1.09 g/cm3 at 20 °C

application(s)

histology
pharma/biopharma processes
pharmaceutical

storage temp.

15-25°C

Related Categories

General description

We offer a range of high quality critical raw materials plus the documentation and expertise to help our customers meet stringent regulatory requirements. Our SAFC® portfolio of high-quality products withstands strict quality control procedures.

Application

Formaldehyde can be used for virus inactivation in vaccine production.

Linkage

Replaces: 1.04002.2507; 1.04002.9187

Legal Information

Emprove is a registered trademark of Merck KGaA, Darmstadt, Germany
SAFC is a registered trademark of Merck KGaA, Darmstadt, Germany

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signalword

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Carc. 1B - Eye Dam. 1 - Muta. 2 - Skin Corr. 1B - Skin Sens. 1 - STOT SE 1 - STOT SE 3

target_organs

Eyes,Central nervous system, Respiratory system

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

143.6 °F - closed cup

flash_point_c

62 °C - closed cup

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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João M Fernandes Neto et al.
Nature communications, 11(1), 3157-3157 (2020-06-24)
Resistance to targeted cancer drugs is thought to result from selective pressure exerted by a high drug dose. Partial inhibition of multiple components in the same oncogenic signalling pathway may add up to complete pathway inhibition, while decreasing the selective

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