Y0001304
Methansulfonsäure-butylester
European Pharmacopoeia (EP) Reference Standard
Synonym(e):
NSC 36060
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Alle Fotos(1)
About This Item
Empirische Formel (Hill-System):
C5H12O3S
CAS-Nummer:
Molekulargewicht:
152.21
UNSPSC-Code:
41116107
NACRES:
NA.24
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Qualität
pharmaceutical primary standard
API-Familie
imatinib
Hersteller/Markenname
EDQM
Anwendung(en)
pharmaceutical (small molecule)
Format
neat
Lagertemp.
2-8°C
SMILES String
[S](=O)(=O)(OCCCC)C
InChI
1S/C5H12O3S/c1-3-4-5-8-9(2,6)7/h3-5H2,1-2H3
InChIKey
LFLBHTZRLVHUQC-UHFFFAOYSA-N
Allgemeine Beschreibung
This product is provided as delivered and specified by the issuing Pharmacopoeia. All information provided in support of this product, including SDS and any product information leaflets have been developed and issued under the Authority of the issuing Pharmacopoeia.For further information and support please go to the website of the issuing Pharmacopoeia.
Anwendung
Butyl methanesulfonate EP Reference standard, intended for use in laboratory tests only as specifically prescribed in the European Pharmacopoeia.
Verpackung
The product is delivered as supplied by the issuing Pharmacopoeia. For the current unit quantity, please visit the EDQM reference substance catalogue.
Sonstige Hinweise
Sales restrictions may apply.
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Produkt-Nr.
Beschreibung
Preisangaben
Lagerklassenschlüssel
10 - Combustible liquids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
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Analysenzertifikate (COA)
Lot/Batch Number
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International journal of cancer, 28(1), 105-110 (1981-07-15)
The influence of pregnant mare serum gonadotropin (PSGM) on the induction of ovarian tumors by carcinogen(DMBA) and/or mutagens (EMS and BMS) has been studied in Swiss albino mice. Priming of the ovaries of 6-week-old mice with PMSG (50 IU/mouse) 24
J C Ball et al.
Environmental and molecular mutagenesis, 13(2), 100-106 (1989-01-01)
This report describes experiments in which a chiral alkyl methanesulfonate was used to investigate possible mechanisms by which alkylating agents cause their mutagenic, cytotoxic, and clastogenic effects. Optically active enantiomers and the racemic mixture of 2-butyl methanesulfonate (2-BMS) were cytotoxic
H Hoppe et al.
Mutation research, 250(1-2), 411-421 (1991-09-11)
Cells of the human lymphoblast line WI-L2 and its derivative TK-6 were synchronized by centrifugal elutriation and cell-cycle dependent mutation to 6TGR (HPRT) and OUAR (Na+, K+ ATPase) measured. Bromodeoxyuridine induced 6TGR and OUAR mutations within S phase while butylmethyl-sulfonate
R Saffhill
Carcinogenesis, 5(5), 621-625 (1984-05-01)
The reaction of N-n-butyl-N-nitrosourea ( BNU ) and n-butyl methanesulphonate (BMS) with DNA has been investigated. In addition to the expected n- butylpurines formed on reaction with BNU some rearranged sec-butyl-adducts were also observed, indicating that a carbonium ion is
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