Neutral Formalin Buffered Solution - 10% , CAS No.50-00-0

CAS: 50-00-0 Cat. No.: F301880 Formule: CH₂O Poids moléculaire: 30.03 Beilstein Registry Number: 1209228 Numéro CE: 200-001-8 PubChem CID: 712

GRADE & PURITY 10%

Synonyms

Durine | Formalin (JP17) | Formalin-loesungen [German] | Hercules 37M6-8 | DTXSID7020637 | F-gen | Formalin 40 | NSC 298885 | 1HG84L3525 | EINECS 200-001-8 | Oxomethylene | Dormol | H2CO | DSSTox_CID_637 | Formaldehyde [USP] | formaldhyde | Aldehyd mraven

Storage

Protected from light,Room temperature

Shipped In

FedEx DG Service

Specifications

Synonymes

Durine | Formalin (JP17) | Formalin-loesungen [German] | Hercules 37M6-8 | DTXSID7020637 | F-gen | Formalin 40 | NSC 298885 | 1HG84L3525 | EINECS 200-001-8 | Oxomethylene | Dormol | H2CO | DSSTox_CID_637 | Formaldehyde [USP] | formaldhyde | Aldehyd mraven

Spécifications et pureté

10%

Conditions de stockage de stockage

Protected from light,Room temperature

Expédié en

FedEx DG Service

Noms et identifiants

Pubchem Sid

508811740

PH

7.25-7.35

Sourires canoniques

C=O

IUPAC Name

formaldehyde

InChIKey

WSFSSNUMVMOOMR-UHFFFAOYSA-N

INCHI

1S/CH2O/c1-2/h1H2

Isomères SMILES

C=O

WGK Allemagne

2

RTECS

LP8925000

PubChem CID

712

Numéro ONU

2209

Groupe d'emballage

III

Poids moléculaire

30.03

Beilstein

1209228

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic oxygen compounds
    • Classe Organooxygen compounds
      • Subclass Carbonyl compounds

• Kingdom: Organic compounds
• Superclass: Organic oxygen compounds
• Classe: Organooxygen compounds
• Subclass: Carbonyl compounds
• Intermediate Tree Nodes: Not available
• Direct Parent: Carbonyl compounds
• Alternative Parents: Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Organic oxide - Hydrocarbon derivative - Carbonyl group - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as carbonyl compounds. These are organic compounds containing a carbonyl group, with the general structure RC(=O)R', where R=organyl, R'=H, N, O, organyl group or halide group.
• External Descriptors: an n-alkanal

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Cibles associées (humaines)

TRPA1 Tclin Transient receptor potential cation channel subfamily A member 1 (0 Activities)

Discover Target: TRPA1

Activity Type	Activity Value -log(M)	Mechanism of Action	Activity Reference	Publications (PubMed IDs)

ACHE Tclin Acetylcholinesterase (18204 Activities)

Discover Target: ACHE

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MPO Tchem Myeloperoxidase (1002 Activities)

Discover Target: MPO

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

NCI/ADR-RES (33767 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

MIA PaCa-2 (5949 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ALPL Tchem Alkaline phosphatase, tissue-nonspecific isozyme (1551 Activities)

Discover Target: ALPL

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cibles associées (non humaines)

Carboxylesterase (379 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Pseudomonas aeruginosa (123386 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Pseudomonas putida (467 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Staphylococcus aureus (210822 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Streptococcus pyogenes (16140 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Plasmodium falciparum (966862 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mécanismes d'action

Propriétés chimiques et physiques

• Sensibilité: Light sensitive.
• Indice de réfraction: 1.3755-1.3775
• Point d'éclair (°C): 64°C
• Point d'ébullition (°C): 97°C
• Point de fusion (°C): -15°C
• Poids moléculaire: 30.026 g/mol
• XLogP3: 1.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 30.0106 Da
• Monoisotopic Mass: 30.0106 Da
• Topological Polar Surface Area: 17.100 Ų
• Heavy Atom Count: 2
• Formal Charge: 0
• Complexity: 2.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1