Amylin(human), 25-L-proline-28-L-proline-29-L-proline-, acetate (salt), hydrate (9CI) | CAS No. 196078-30-5

Amylin(human), 25-L-proline-28-L-proline-29-L-proline-, acetate (salt), hydrate (9CI)

Basic Information

CAS Number

196078-30-5

Molecular Formula

C173H273N51O56S2

Molecular Weight

4027.46 g/mol

EINECS

251-228-4

AD

Basic Physical Properties

Melting Point

>175°C (dec.)

CCC(C(NC(C1N(C(CNC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(NC(C(N)CCCCN)=O)CS)=O)CC(N)=O)=O)C(O)C)=O)C)=O)C(O)C)=O)CS)=O)C)=O)C(O)C)=O)CCC(N)=O)=O)CCCNC(N)=N)=O)CC(C)C)=O)C)=O)CC(N)=O)=O)CC2=CC=CC=C2)=O)CC(C)C)=O)C(C)C)=O)CC2N=CNC=2)=O)CO)=O)CO)=O)CC(N)=O)=O)CC(N)=O)=O)CC2=CC=CC=C2)=O)=O)CCC1)=O)C(NC(C(N1C(C(N2C(C(NC(C(NC(C(NC(C(NCC(NC(C(NC(C(NC(C(NC(C(N)=O)CC3=CC=C(O)C=C3)=O)C(O)C)=O)CC(N)=O)=O)CO)=O)=O)C(C)C)=O)CC(N)=O)=O)C(O)C)=O)CCC2)=O)CCC1)=O)CC(C)C)=O)C

InChI

InChI=1S/C171H269N51O53S2/c1-21-81(12)130(163(268)207-110(56-78(6)7)169(274)222-53-33-42-118(222)170(275)221-52-32-41-117(221)160(265)219-135(89(20)230)167(272)206-109(66-125(180)238)151(256)212-128(79(8)9)161(266)186-68-126(239)192-111(70-223)154(259)203-107(64-123(178)236)152(257)218-134(88(19)229)166(271)195-98(136(181)241)57-92-43-45-94(231)46-44-92)214-159(264)116-40-31-51-220(116)127(240)69-187-141(246)101(58-90-34-24-22-25-35-90)199-148(253)105(62-121(176)234)201-149(254)106(63-122(177)235)202-155(260)112(71-224)209-156(261)113(72-225)208-146(251)103(60-93-67-184-75-188-93)205-162(267)129(80(10)11)213-150(255)100(55-77(4)5)198-145(250)102(59-91-36-26-23-27-37-91)200-147(252)104(61-120(175)233)196-137(242)82(13)189-144(249)99(54-76(2)3)197-142(247)96(39-30-50-185-171(182)183)193-143(248)97(47-48-119(174)232)194-165(270)132(86(17)227)215-138(243)83(14)190-157(262)114(73-276)211-168(273)133(87(18)228)216-139(244)84(15)191-164(269)131(85(16)226)217-153(258)108(65-124(179)237)204-158(263)115(74-277)210-140(245)95(173)38-28-29-49-172/h22-27,34-37,43-46,67,75-89,95-118,128-135,223-231,276-277H,21,28-33,38-42,47-66,68-74,172-173H2,1-20H3,(H2,174,232)(H2,175,233)(H2,176,234)(H2,177,235)(H2,178,236)(H2,179,237)(H2,180,238)(H2,181,241)(H,184,188)(H,186,266)(H,187,246)(H,189,249)(H,190,262)(H,191,269)(H,192,239)(H,193,248)(H,194,270)(H,195,271)(H,196,242)(H,197,247)(H,198,250)(H,199,253)(H,200,252)(H,201,254)(H,202,260)(H,203,259)(H,204,263)(H,205,267)(H,206,272)(H,207,268)(H,208,251)(H,209,261)(H,210,245)(H,211,273)(H,212,256)(H,213,255)(H,214,264)(H,215,243)(H,216,244)(H,217,258)(H,218,257)(H,219,265)(H4,182,183,185)

InChIKey

NRKVKVQDUCJPIZ-UHFFFAOYSA-N

LogP

-3.45320

Topological Polar Surface Area

1690.6399999999992 Ų

Hydrogen Bond Donor/Acceptor

67 / 104

Complexity

9620

Synonyms & References

English

  • AMYLIN (HUMAN), 25-L-PROLINE-28-L-PROLINE-29-L-PROLINE-, ACETATE (SALT), HYDRATE
  • pramlintide acetate
  • pramlintide acetate hydrate
  • 25-L-Proline-28-L-proline-29-L-proline-aMylin (huMan) Acetate Hydrate
  • AC-137 Acetate Hydrate, SyMlin Acetate Hydrate
  • Tripo-aMylin Acetate Hydrate
  • Pramlintide Acetate, Amylin Rat
  • Pramlintide?Acetate impurity
  • Pramlintide Acetate
  • Pramlintide
  • Pramlintide Acetate Hydrate

MDL Number

MFCD08460172

EC Number

251-228-4

FAQ

What are the physical and chemical properties of Amylin(human), 25-L-proline-28-L-proline-29-L-proline-, acetate (salt), hydrate (CAS: 196078-30-5)?

Amylin(human), 25-L-proline-28-L-proline-29-L-proline-, acetate (salt), hydrate is a crystalline compound with a molecular weight of approximately 2274.5 g/mol. It has a high solubility in water and lower solubility in organic solvents. The compound is relatively stable under normal conditions but can degrade upon exposure to heat and acid. It exhibits strong reactivity with bases and is susceptible to hydrolysis under certain conditions.

How is Amylin(human), 25-L-proline-28-L-proline-29-L-proline-, acetate (salt), hydrate (CAS: 196078-30-5) typically synthesized?

Amylin(human), 25-L-proline-28-L-proline-29-L-proline-, acetate (salt), hydrate is synthesized through a multi-step process involving peptide synthesis and acetylation. Commonly, solid-phase peptide synthesis is used, followed by deprotection and acetylation. This process typically yields a product with high purity and selectivity, though careful monitoring of reaction conditions is necessary to achieve optimal yields.

What industries use Amylin(human), 25-L-proline-28-L-proline-29-L-proline-, acetate (salt), hydrate (CAS: 196078-30-5)?

Amylin(human), 25-L-proline-28-L-proline-29-L-proline-, acetate (salt), hydrate is predominantly used in the pharmaceutical industry for the development and production of pharmaceutical products. It may also find applications in research and development for diagnostic tools and sensors. Its specific use in polymers and semiconductors is limited but not entirely ruled out.

What precautions should be taken when handling Amylin(human), 25-L-proline-28-L-proline-29-L-proline-, acetate (salt), hydrate (CAS: 196078-30-5)?

When handling Amylin(human), 25-L-proline-28-L-proline-29-L-proline-, acetate (salt), hydrate, it is essential to wear appropriate personal protective equipment (PPE), including gloves, safety goggles, and a lab coat. Work should be conducted in a well-ventilated area or a fume hood to minimize inhalation risks. Spills should be cleaned up immediately using appropriate absorbent materials. Always consult the Safety Data Sheet (SDS) for detailed handling and disposal instructions.

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