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25126-51-6

undecaprenyl phosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 25126-51-6 Structure

  • Basic information

    1. Product Name: undecaprenyl phosphate
    2. Synonyms: undecaprenyl phosphate;undecaprenyl dihydrogen phosphate
    3. CAS NO:25126-51-6
    4. Molecular Formula: C55H91O4P
    5. Molecular Weight: 847.282401
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 25126-51-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 838.8°Cat760mmHg
    3. Flash Point: 461.1°C
    4. Appearance: /
    5. Density: 0.952g/cm3
    6. Vapor Pressure: 4.66E-31mmHg at 25°C
    7. Refractive Index: 1.513
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: undecaprenyl phosphate(CAS DataBase Reference)
    11. NIST Chemistry Reference: undecaprenyl phosphate(25126-51-6)
    12. EPA Substance Registry System: undecaprenyl phosphate(25126-51-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 25126-51-6(Hazardous Substances Data)

25126-51-6 Usage

Definition

ChEBI: The all-trans-isomer of undecaprenyl phosphate.

Check Digit Verification of cas no

The CAS Registry Mumber 25126-51-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,1,2 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 25126-51:
(7*2)+(6*5)+(5*1)+(4*2)+(3*6)+(2*5)+(1*1)=86
86 % 10 = 6
So 25126-51-6 is a valid CAS Registry Number.
InChI:InChI=1/C55H91O4P/c1-45(2)23-13-24-46(3)25-14-26-47(4)27-15-28-48(5)29-16-30-49(6)31-17-32-50(7)33-18-34-51(8)35-19-36-52(9)37-20-38-53(10)39-21-40-54(11)41-22-42-55(12)43-44-59-60(56,57)58/h23,25,27,29,31,33,35,37,39,41,43H,13-22,24,26,28,30,32,34,36,38,40,42,44H2,1-12H3,(H2,56,57,58)/b46-25+,47-27+,48-29+,49-31+,50-33+,51-35+,52-37+,53-39+,54-41+,55-43+

25126-51-6SDS

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 undecaprenyl dihydrogen phosphate

1.2 Other means of identification

Product number -
Other names [(2E,6E,10E,14E,18E,22E,26E,30E,34E,38E)-3,7,11,15,19,23,27,31,35,39,43-undecamethyltetratetraconta-2,6,10,14,18,22,26,30,34,38,42-undecaenyl] dihydrogen phosphate

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:25126-51-6 SDS

25126-51-6Downstream Products

25126-51-6Relevant articles and documents

BIOSYNTHESIS OF A D-GLUCOSYL POLYISOPRENYL DIPHOSPHATE IN PARTICULATE PREPARATIONS OF MICROCOCCUS LYSODEIKTICUS

Yamazaki, Tatsumi,Laske, Douglas W.,Herscovics, Annette,Warren, Christopher D.,Jeanloz, Roger W.

, p. 159 - 170 (2007/10/02)

Particulate fractions of Micrococcus lysodeikticus incubated with UDP-D-glucose incorporated radioactivity into a chloroform-methanol-soluble, low-mol. wt. compound, and into a polymer.The low-mol. wt. compound consisted of a glucolipid that was extremely labile to mild acid hydrolysis with the formation of D-glucose, and to mild alkali, yielding 14C-labeled α-D-glucopyranose 1,2-phosphate and D-glucose 2-phosphate.The labeled glucolipid was eluted from a DEAE-cellulose column at a salt concentration higher than that required by synthetic ficaprenyl (D-glucopyranosyl phosphate), and it migrated more slowly than the latter compound in t.l.c.Formation of glucolipid was stimulated by exogenous ficaprenyl phosphate, but not by C55-dolichyl phophate.These results suggest that the glucolipid has the characteristic properties of a polyisoprenyl glucosyl diphosphate.

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