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77700-90-4

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77700-90-4 Usage

Chemical composition

1,3-Dimyristin is composed of two myristic acid molecules linked by an ether bond.

Physical state

It is a white, waxy solid.

Solubility

Insoluble in water but soluble in organic solvents.

Common uses

a. Emulsifying agent
b. Base for cosmetic and personal care products
c. Lubricant
d. Component in pharmaceuticals and dietary supplements

Applications

a. Lotions
b. Creams
c. Lip balms

Properties

a. Ability to form stable emulsions
b. Moisturizing properties

Popularity

Widely used in cosmetic and personal care formulations due to its emulsifying and moisturizing properties.

Check Digit Verification of cas no

The CAS Registry Mumber 77700-90-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,7,0 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 77700-90:
(7*7)+(6*7)+(5*7)+(4*0)+(3*0)+(2*9)+(1*0)=144
144 % 10 = 4
So 77700-90-4 is a valid CAS Registry Number.

77700-90-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name triosmiumplatinum(μ-hydrido)2(carbonyl)10(P(cyclohexyl)3)(carbonyl)

1.2 Other means of identification

Product number -
Other names -

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:77700-90-4 SDS

77700-90-4Upstream product

77700-90-4Downstream Products

77700-90-4Relevant articles and documents

Chemistry of the Unsaturated Cluster Compound >; X-Ray Crystal Structures of >, >, and > (Two Isomers)

Farrugia, Louis J.,Green, Michael,Hankey, David R.,Murray, Martin,Orpen, A. Guy,Stone, F. Gordon A.

, p. 177 - 190 (1985)

Reactions of the unsaturated cluster compound > with hydrogen and with diazomethane have been investigated, and the structures of the products determined by X-ray diffraction.The structure of the previously prepared carbon monoxide adduct P(cyclo-C6H11)3>> has also been established.The latter species, which is formed in a readily reversed reaction, has a 'butterfly' arrangement of the metal atoms with the platinum atom at a wing-tip position.One hydrido-ligand bridges the Os-Os vector of the body of the butterfly, and the other an Os-Pt edge.The latter is cis to the P(cyclo-C6H11)3 group on the platinum, which also carries a CO ligand.The osmium atom at the other wing-tip is ligated by four CO groups, and the remaining two Os are each terminally bonded to three carbonyls.The hydrogen adduct > is also formed reversibly but in contrast with the product from carbon monoxide has a closo-tetrahedral metal core.The hydrido-ligands occupy edge-bridging sites on the cluster framework, with two bridging Os-Pt vectors and two bridging Os-Os vectors.Thus the M4 tetrahedron has D2d symmetry with two short unbridged edges and four longer bridged edges.Diazomethane readily adds to > to give the complex > which exists as an equilibrium mixture of two isomeric forms (orange-yellow and red crystals).Both species have a closo distorted tetrahedral geometry for the metal atoms, with the methylene group bridging an Os-Os edge cisoid to the P(cyclo-C6H11)3 ligand on the platinum in the orange-yellow form and transoid to the phosphine group in the red isomer.The relative positions of the hydrido-ligands also differ.In the orange-yellow form they bridge the remaining two Os-Os edges, while although not located directly in the red isomer, being assigned on potential-energy grounds, they bridge an Os-Os edge and the Os-Pt edge cis to the P(cyclo-C6H11)3 ligand.N.m.r. studies reveal that the two isomers maintain these solid-state structures in solution.The mechanism of formation of the two isomers is discussed in the context of the orange-yellow form being the kinetically controlled product, which after several days in solution establishes a 1:4 equilibrium with the red form.

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