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DI-1-ADAMANTYLPHOSPHINE

CAS No.
131211-27-3
Chemical Name:
DI-1-ADAMANTYLPHOSPHINE
Synonyms
Diadamantylphosphine;DI-1-ADAMANTYLPHOSPHINE;Bis(adamant-1-yl)phosphine;Di-1-adamantylphosphine>Di-1-adamantylphosphine,97%;Di(adamantan-1-yl)phosphine;Di-1-adamantylphosphine 97%;Bis(1-adamantyl)phosphine, 98%;Di-1-adamantylphosphine,min.97%;Di-1-adamantylphosphine, min. 97%
CBNumber:
CB4371982
Molecular Formula:
C20H31P
Molecular Weight:
302.43
MDL Number:
MFCD06658117
MOL File:
131211-27-3.mol
MSDS File:
SDS
Last updated:2026-01-13 11:21:13
Product description Number Pack Size Price
Di-1-adamantylphosphine 97% 695823 500mg $134.32
Di-1-adamantylphosphine 97% 695823 2g $517.04
Di-1-adamantylphosphine >95.0%(GC) D4781 200mg $43
Di-1-adamantylphosphine >95.0%(GC) D4781 1g $126
Di-1-adamantylphosphine, min. 97% 15-0954 250mg $69
More product size

DI-1-ADAMANTYLPHOSPHINE Properties

Melting point 181-185 °C
Boiling point 407.8±12.0 °C(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
form Powder
color white
Sensitive air sensitive
InChI InChI=1S/C20H31P/c1-13-2-15-3-14(1)8-19(7-13,9-15)21-20-10-16-4-17(11-20)6-18(5-16)12-20/h13-18,21H,1-12H2
InChIKey RRRZOLBZYZWQBZ-UHFFFAOYSA-N
SMILES P(C12CC3CC(CC(C3)C1)C2)C12CC3CC(CC(C3)C1)C2
UNSPSC Code 12350000
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS06
Signal word  Danger
Hazard statements  H301+H311+H331-H315-H319-H335
Precautionary statements  P261-P280-P301+P310-P302+P352+P312-P304+P340+P311-P305+P351+P338
target organs Respiratory system
PPE Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Hazard Codes  T
Risk Statements  23/24/25-36/37/38
Safety Statements  36/37/39-45
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
HS Code  2931.90.9051
HazardClass  6.1
PackingGroup 
Storage Class 6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard Classifications Acute Tox. 3 Dermal
Acute Tox. 3 Inhalation
Acute Tox. 3 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3

DI-1-ADAMANTYLPHOSPHINE price More Price(18)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 695823 Di-1-adamantylphosphine 97% 131211-27-3 500mg $134.32 2025-07-31 Buy
Sigma-Aldrich 695823 Di-1-adamantylphosphine 97% 131211-27-3 2g $517.04 2025-07-31 Buy
TCI Chemical D4781 Di-1-adamantylphosphine >95.0%(GC) 131211-27-3 200mg $43 2025-07-31 Buy
TCI Chemical D4781 Di-1-adamantylphosphine >95.0%(GC) 131211-27-3 1g $126 2025-07-31 Buy
Strem Chemicals 15-0954 Di-1-adamantylphosphine, min. 97% 131211-27-3 250mg $69 2024-03-01 Buy
Product number Packaging Price Buy
695823 500mg $134.32 Buy
695823 2g $517.04 Buy
D4781 200mg $43 Buy
D4781 1g $126 Buy
15-0954 250mg $69 Buy

DI-1-ADAMANTYLPHOSPHINE Chemical Properties,Uses,Production

Appearance

White Powder

Uses

Di-1-adamantylphosphine is a useful research chemical.

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand

Synthesis

DI-1-ADAMANTYLPHOSPHINIC CHLORIDE

126683-99-6

DI-1-ADAMANTYLPHOSPHINE

131211-27-3

The general procedure for the synthesis of di-1-adamantylphosphine using bis(1-adamantyl)phosphinic chloride as starting material was as follows: at -10 °C, LiAlH4 (2.54 g, 67.0 mmol) was slowly added to a cooled solution of bis(1-adamantyl)phosphinic chloride (10.00 g, 28.3 mmol) dissolved in dry THF (120 cm3) over 90 min. The reaction mixture was gradually warmed to room temperature and stirred continuously for 20 hours. Subsequently, the gray suspension was re-cooled to -10 °C and a mixed solution consisting of concentrated hydrochloric acid (5 cm3) and degassed water (50 cm3) was slowly added via syringe (due to the exothermic nature of the reaction, the initial rate of addition needed to be very slow), at which point a two-phase system was formed, with solids visible in the lower phase. To further improve the phase separation, concentrated hydrochloric acid (5 cm3) was added. The upper organic phase was removed using a flat cannula and the remaining organic phase was dried with MgSO4 and filtered through a cannula. Volatiles were removed under vacuum to give a white powdery product which was separated in a glove box. The final product yield was 6.00 g in 70% yield. The product showed a single peak (δ=17 ppm) by 31P NMR and was 100% pure. The molecular weight of the product was 302.44.

References

[1] Phosphorus, Sulfur and Silicon and the Related Elements, 1995, vol. 102, # 1-4, p. 211 - 216
[2] Phosphorus, Sulfur and Silicon and the Related Elements, 1993, vol. 81, # 1-4, p. 141 - 148
[3] Organometallics, 2018, vol. 37, # 19, p. 3243 - 3247
[4] Patent: US9802185, 2017, B2. Location in patent: Page/Page column 38; 39
[5] J. Gen. Chem. USSR (Engl. Transl.), 1990, vol. 60, # 8.1, p. 1603 - 1606

281-23-2
131211-27-3
Synthesis of DI-1-ADAMANTYLPHOSPHINE from Adamantane
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View Lastest Price from DI-1-ADAMANTYLPHOSPHINE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
DI-1-ADAMANTYLPHOSPHINE pictures 2025-12-23 DI-1-ADAMANTYLPHOSPHINE
131211-27-3
US $0.00-0.00 / KG 1KG 0.98 500kg XINXIANG RUNYU MATERIAL CO., LTD.
Bis(1-adamantyl)phosphine   pictures 2025-12-12 Bis(1-adamantyl)phosphine
131211-27-3
US $1.00-0.00 / KG 1KG 99% 20 tons Shaanxi Dideu Medichem Co. Ltd
DI-1-ADAMANTYLPHOSPHINE pictures 2025-10-13 DI-1-ADAMANTYLPHOSPHINE
131211-27-3
US $2.00-5.00 / kg 1kg 99% 100kg ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
DI-1-ADAMANTYLPHOSPHINE Bis(adamant-1-yl)phosphine, Bis(tricyclo[3.3.1.13,7]dec-1-yl)phosphine Di-1-adamantylphosphine, min. 97% Bis(1-adamantyl)phosphine, 98% Di-1-adamantylphosphine 97% Di-1-adamantylphosphine,min.97% Bis(adamant-1-yl)phosphine Diadamantylphosphine Di(adamantan-1-yl)phosphine Di-1-adamantylphosphine,97% Di-1-adamantylphosphine> Phosphine, bis(tricyclo[3.3.1.13,7]dec-1-yl)- 131211-27-3 133211-27-3 C10H152PH C20H31P P-H Achiral Phosphine Alkyl Phosphine organophosphine ligand