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Cyclophosphamide monohydrate - 97%, high purity , DNA inhibitor, CAS No.6055-19-2, DNA inhibitor

  • ≥97%
Item Number
C106991
Grouped product items
SKUSizeAvailabilityPrice Qty
C106991-1g
1g
In stock
$22.90
C106991-5g
5g
In stock
$87.90
C106991-25g
25g
In stock
$294.90
C106991-100g
100g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$1,060.90
C106991-500g
500g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$4,770.90

Basic Description

SynonymsCyclophosphamide monohydrate|6055-19-2|Cyclophosphamide hydrate|Neosar|Endoxan monohydrate|Revimmune|2-(Bis(2-chloroethyl)amino)-1,3,2-oxazaphosphinane 2-oxide hydrate|Cyclophosphamide (hydrate)|Ciclophosphamide hydrat|Ciclofosfamide|Cycloblastin|6055-19-
Specifications & Purity≥97%
Storage TempStore at 2-8°C,Argon charged
Shipped InWet ice
Action TypeINHIBITOR
Mechanism of actionDNA inhibitor
Product Description

Cyclophosphamide monohydrate is an alkylating, cytotoxic agent experimentally shown to crosslink DNA, causing strand breakage and inducing mutations. It is also believed to possess immunosuppressive properties. Cyclophosphamide Monohydrate inhibits ALDH1 (aldehyde dehydrogenase 1) through its degradation product acrolein, as well as induces apoptosis in the rat thymus via the Fas/Fas ligand pathway.
An immunosuppressive, cytotoxic apoptosis inducer.

Associated Targets

EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GMNN Tbio Geminin 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RUNX1 Tbio Runt-related transcription factor 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SMAD3 Tchem Mothers against decapentaplegic homolog 3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ALOX15 Tchem Arachidonate 15-lipoxygenase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

APEX1 Tchem DNA-(apurinic or apyrimidinic site) lyase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TARDBP Tchem TAR DNA-binding protein 43 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

NFE2L2 Tchem Nuclear factor erythroid 2-related factor 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KDM4E Tchem Lysine-specific demethylase 4E 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAPK1 Tchem Mitogen-activated protein kinase 1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name N,N-bis(2-chloroethyl)-2-oxo-1,3,2λ5-oxazaphosphinan-2-amine;hydrate
INCHI InChI=1S/C7H15Cl2N2O2P.H2O/c8-2-5-11(6-3-9)14(12)10-4-1-7-13-14;/h1-7H2,(H,10,12);1H2
InChi Key PWOQRKCAHTVFLB-UHFFFAOYSA-N
Canonical SMILES C1CNP(=O)(OC1)N(CCCl)CCCl.O
Isomeric SMILES C1CNP(=O)(OC1)N(CCCl)CCCl.O
WGK Germany 3
RTECS RP6157750
Alternate CAS 6055-19-2,50-18-0 (Parent)
PubChem CID 22420
UN Number 2811
Packing Group I
MeSH Entry Terms (+,-)-2-(bis(2-Chloroethyl)amino)tetrahydro-2H-1,3,2-oxazaphosphorine 2-Oxide Monohydrate;B 518;B-518;B518;Cyclophosphamide;Cyclophosphamide Anhydrous;Cyclophosphamide Monohydrate;Cyclophosphamide, (R)-Isomer;Cyclophosphamide, (S)-Isomer;Cyclophosphane;Cy
Molecular Weight 279.1
Beilstein 4678992
Reaxy-Rn 8167897

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

5 results found

Lot NumberCertificate TypeDateItem
K2217398Certificate of AnalysisNov 03, 2022 C106991
K2217399Certificate of AnalysisNov 03, 2022 C106991
K2217400Certificate of AnalysisNov 03, 2022 C106991
K2217404Certificate of AnalysisNov 03, 2022 C106991
K2217473Certificate of AnalysisNov 03, 2022 C106991

Chemical and Physical Properties

SolubilitySoluble in water (30 mg/ml), ethanol (slightly soluble), benzene (slightly soluble), ethylene glycol (slightly soluble), carbon tetrachloride (slightly soluble), dioxane (slightly soluble), ether (sparingly soluble), acetone (sparingly soluble), alcohol,
SensitivityHeat, Light, Air sensitive.
Flash Point(°F)235.4 °F
Flash Point(°C)113 °C
Boil Point(°C)110°C
Melt Point(°C)49-53°C

Safety and Hazards(GHS)

Pictogram(s) GHS06,   GHS08
Signal Danger
Hazard Statements

H301:Toxic if swallowed

H350:May cause cancer

Precautionary Statements

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P270:Do not eat, drink or smoke when using this product.

P330:Rinse mouth.

P203:Obtain, read and follow all safety instructions before use.

P301+P316:IF SWALLOWED: Get emergency medical help immediately.

P318:if exposed or concerned, get medical advice.

WGK Germany 3
RTECS RP6157750
Reaxy-Rn 8167897
Class 6.1
Merck Index 2747

Related Documents

Solution Calculators