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Safety Information

852503

Sigma-Aldrich

6-Cyanopurine

97%

Synonym(s):

6-Purinecarbonitrile

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About This Item

Empirical Formula (Hill Notation):
C6H3N5
CAS Number:
2036-13-7
Molecular Weight:
145.12
EC Number:
218-005-3
MDL number:
MFCD00005569
UNSPSC Code:
12352100
PubChem Substance ID:
24888324

Assay

97%

form

powder

mp

186-189 °C (lit.)

SMILES string

N#Cc1ncnc2nc[nH]c12

InChI

1S/C6H3N5/c7-1-4-5-6(10-2-8-4)11-3-9-5/h2-3H,(H,8,9,10,11)

InChI key

NHYQQYMSESLQDX-UHFFFAOYSA-N

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PDSCL

Deleterious substance

JAN Code

852503-VAR:
852503-25MG:4548173181325
852503-BULK:
852503-100MG:4548173181318

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Certificates of Analysis (COA)

Lot/Batch Number
14709AE
18568DQ
14617DO
07843TN
07839BZ

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M Alice Carvalho et al.
Organic & biomolecular chemistry, 2(7), 1019-1024 (2004-03-23)
An extremely simple method for the selective synthesis of 9-aryl and 9-alkyl 6-alkoxy or 6-alkoxyformimidoylpurines from the corresponding 6-cyanopurines is described. The reaction is carried out with methanol or ethanol in the presence of DBU. At room temperature, nucleophilic attack
J B Peterson et al.
Journal of bacteriology, 151(3), 1473-1484 (1982-09-01)
A soluble aldehyde dehydrogenase (EC 1.2.1.3) was partially purified from Rhizobium japonicum bacteroids and from free-living R. japonicum 61A76. The enzyme was activated by NAD+, NADH, and dithiothreitol, and it reduced NAD(P)+. Acetaldehyde, propionaldehyde, butyraldehyde, benzaldehyde, and succinic semialdehyde were

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