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CAS

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30470-60-1

ADAMANTANE-D16, also known as labeled adamantane, is a chemical compound derived from the adamantane molecule with deuterium atoms (D16) incorporated into its structure. It is a white waxy solid that serves as a valuable tool in various scientific and pharmaceutical applications due to its unique properties.

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  • 30470-60-1 Structure

  • Basic information

    1. Product Name: ADAMANTANE-D16
    2. Synonyms: ADAMANTANE-D16;ADAMANTANE-D16 (98 ATOM % D)
    3. CAS NO:30470-60-1
    4. Molecular Formula: C10D16
    5. Molecular Weight: 152.33
    6. EINECS: N/A
    7. Product Categories: Alphabetical Listings;Stable Isotopes;Isotope Labeled Compounds;A
    8. Mol File: 30470-60-1.mol

  • Chemical Properties

    1. Melting Point: 209-212 °C (subl.)(lit.)
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: ADAMANTANE-D16(CAS DataBase Reference)
    10. NIST Chemistry Reference: ADAMANTANE-D16(30470-60-1)
    11. EPA Substance Registry System: ADAMANTANE-D16(30470-60-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 30470-60-1(Hazardous Substances Data)

30470-60-1 Usage

Uses

Used in Analytical Chemistry:
ADAMANTANE-D16 is used as an internal standard for the quantification of adamantane by gas chromatography (GC) or liquid chromatography (LC) mass spectrometry. Its incorporation of deuterium atoms allows for accurate measurement and comparison of the target compound's concentration in a given sample.
Used in Pharmaceutical Applications:
ADAMANTANE-D16 serves as a key component in the fast catalytic hydroxylation of hydrocarbons with ruthenium porphyrins. This process is essential in the synthesis of various pharmaceutical compounds.
Additionally, unlabeled adamantane derivatives, which are structurally similar to ADAMANTANE-D16, have been used to treat influenza and act as N-methyl-D-aspartate (NMDA) receptor channel blockers. These blockers have a wide range of pharmaceutical applications, including the treatment of neurological disorders and pain management.

Check Digit Verification of cas no

The CAS Registry Mumber 30470-60-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,4,7 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30470-60:
(7*3)+(6*0)+(5*4)+(4*7)+(3*0)+(2*6)+(1*0)=81
81 % 10 = 1
So 30470-60-1 is a valid CAS Registry Number.

30470-60-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,2,3,4,4,5,6,6,7,8,8,9,9,10,10-hexadecadeuterioadamantane

1.2 Other means of identification

Product number -
Other names Adamantane-d16

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:30470-60-1 SDS

30470-60-1Upstream product

30470-60-1Relevant articles and documents

Multiple deuteration of alkanes synergistically-catalyzed by platinum and rhodium on carbon as a mixed catalytic system

Yamada, Tsuyoshi,Sawama, Yoshinari,Shibata, Kyoshiro,Morita, Kosuke,Monguchi, Yasunari,Sajiki, Hironao

, p. 13727 - 13732 (2015/02/19)

We have accomplished an efficient and mild multiple deuteration method for alkanes catalyzed by the combined use of heterogeneous platinum on carbon (Pt/C) and rhodium on carbon (Rh/C) catalysts in i-PrOD-d8 and D2O as a mixed solvent. The present multi-deuteration could be initiated by the transition metal-catalyzed dedeuteration of i-PrOD-d8 to produce D2 and the subsequent C-H bond activation of alkanes catalyzed by the Pt/C and/or Rh/C-D2 complex. This method could be applied to the deuteration of wide variety of linear, branched and cyclic alkanes as useful deuterated materials under mild conditions. This journal is

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