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Sigma-Aldrich

Fluoromethane-13C

99 atom % 13C

Synonyme(s) :

Methyl-13C fluoride

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About This Item

Formule linéaire :
13CH3F
Numéro CAS:
20666-44-8
Poids moléculaire :
35.03
Numéro MDL:
MFCD00083967
Code UNSPSC :
12352101
ID de substance PubChem :
24872480
Nomenclature NACRES :
NA.12

Densité de vapeur

1.231 (vs air)

Pression de vapeur

44.2 atm ( 21.1 °C)

Pureté isotopique

99 atom % 13C

Point d'ébullition

−77.9 °C (lit.)

Pf

−141.8 °C (lit.)

Changement de masse

M+1

Chaîne SMILES 

[13CH3]F

InChI

1S/CH3F/c1-2/h1H3/i1+1

Clé InChI

NBVXSUQYWXRMNV-OUBTZVSYSA-N

Catégories apparentées

Conditionnement

100 mL quantity is packaged in a 25 mL Sure/Pac™ cylinder with brass 1/4" male NPT valve. Nominal gas pressure at 21ºC is 32 psig for 100 mL. This pressure is slightly above atmospheric pressure. Care must be taken when extracting this product from the cylinder.
This product may be available from bulk stock and can be packaged on demand. For information on pricing, availability and packaging, please contact Stable Isotopes Customer Service.

Produits recommandés

Brass hose adapter Z146811 or brass body mini gas regulator Z513539 is recommended.

Informations légales

Sure/Pac is a trademark of Sigma-Aldrich Co. LLC

Raccord cannelé

Réf. du produit
Description
Tarif

Z146811

Hose adapter, brass

Régulateur

Réf. du produit
Description
Tarif

Pictogrammes

FlameGas cylinder
GHS02,GHS04

Mention d'avertissement

Danger

Mentions de danger

H220,H280

Classification des risques

Flam. Gas 1 - Press. Gas Liquefied gas

Code de la classe de stockage

2A - Gases

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Faceshields, Gloves, multi-purpose combination respirator cartridge (US)

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.

Consulter la Bibliothèque de documents

Jongwook Choi et al.
Science (New York, N.Y.), 332(6037), 1545-1548 (2011-06-28)
Carbon-fluorine bonds are the strongest known single bonds to carbon and as a consequence can prove very hard to cleave. Alhough vinyl and aryl C-F bonds can undergo oxidative addition to transition metal complexes, this reaction has appeared inoperable with
Robert E Rosenberg
The journal of physical chemistry. A, 116(44), 10842-10849 (2012-10-13)
Fluorinated organic compounds have become increasingly important in the pharmaceutical and agricultural industries. However, even the simplest aspects of these compounds are still not well understood. For instance, it is an open question as to whether fluoroorganics can form a
Xiang Zhao et al.
The journal of physical chemistry. A, 110(36), 10607-10618 (2006-09-08)
Reactions of CH(3)F have been surveyed systematically at room temperature with 46 different atomic cations using an inductively coupled plasma/selected-ion flow tube tandem mass spectrometer. Rate coefficients and product distributions were measured for the reactions of fourth-period atomic ions from
G K Surya Prakash et al.
Journal of the American Chemical Society, 133(26), 9992-9995 (2011-06-09)
The trifluoromethyl substituent has been incorporated into quinidine as a conformational stabilizer and a probe to provide straightforward insight into the conformational behavior of cinchona alkaloids. By significantly decreasing the rotation rate of the quinoline-carbinol bond, the relatively bulky CF(3)
G K Surya Prakash et al.
Proceedings of the National Academy of Sciences of the United States of America, 106(11), 4090-4094 (2009-02-25)
Highly efficient stereoselective 1,4-addition of racemic alpha-fluoro-alpha-nitro(phenylsulfonyl)methane (FNSM) as a fluoromethyl pronucleophile to alpha,beta-unsaturated ketones using a wide range of chiral organobifunctional catalysts under moderate conditions in the absence of an additional base has been achieved. A series of catalysts
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